Publications

Found 76 results

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2007
1996
MUNGE PROFMUKUNYAD. "Mibey, R.K., K.K. Kokwaro and D.M. Mukunya, 1996. A new species and four new records of Asterina from Kenya. Nova Hedwigia 62: 144 .". In: International Journal at Biochephysics vol.10, 30-33 (2000). Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1996. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1992
1990
Buruchara RA;, Mukunya DM;, Gathuru EM. "Bacterial black spot of mangoes in Kenya."; 1990.
MUNGE PROFMUKUNYAD. "Mutitu, E.W., D.M. Mukunya and S.O. Keya, 1990. Effect of moisture on Fusarium yellows of beans caused by Fusarium oxysporum f.sp. phaseoli in Kenya. Accepted for publication in the Kenya National Academy Journal Series B. for 1990.". In: International Journal at Biochephysics vol.10, 30-33 (2000). Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1990. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1989
MUNGE PROFMUKUNYAD. "Arama, F.P., D. M. Mukunya and R.A. Buruchara, 1989. The influence of temperature on infection of Rhynchosprium sequels on susceptible and resistant Kenya barley varieties.". In: Proceedings of 1st Plant Pathology Society of Kenya Conference, 23-24 Nov. 1989. Nairobi, Kenya. 15P. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1989. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Kihurani, A.W., D.M. Mukunya and R.A. Burucahra, 1989. Evaluation of bean cultivars for resistance to rust.". In: Proceedings of the 1st Plant Pathology Society of Kenya Conference, 23 . Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1989. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1989. Plant health for increased crop production and a healthy nation. A keynote address. The 1st Plant Pathology Society of Kenya Conference Proceedings, 23 .". In: International Journal at Biochephysics vol.10, 30-33 (2000). Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1989. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mutitu, E.W., D.M. Mukunya and E.M. Gathuru, 1989. Effect of organic amendments on Fusarium yellow disease on the bean host. Discovery and Innovation Vol 1: 67 .". In: International Journal at Biochephysics vol.10, 30-33 (2000). Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1989. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Njiru, J. and D.M. Mukunya, 1989. Variation in Collectotrichum coffeanum, the cause of coffee berry disease as shown by eletrophoretic separation of extracellular proteins of different isolates. Proceedings of the 1st Plant Pathology Society of Kenya Conf.". In: Proceedings of the 1st Plant Pathology Society of Kenya Conference, 23 . Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1989. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1988
Mukunya DM, Gathuru EM, Omunyin ME. "Reactions of cultivars of bean (Phaseolus vulgaris L.) to bean common mosaic virus (BCMV).". 1988. Abstract

3 plants of each cultivar were raised in pots filled with sterile soil, 451 bean cultivars were tested in all. Inoculum was prepared from 30-day-old plants of P. vulgaris. Seedlings of test varieties were inoculated when 2 weeks old, the inoculum consisted of 14 virus isolates ground in 0.01 m phosphate buffer, pH 7.3 and manually inoculated onto primary leaves of seedlings dusted with 500 mesh carborundum. A cultivar was rated resistant if no systemic infection could be detected and susceptible if it became systemically infected or if the presence of the virus in inoculated leaves of plants without systemic symptoms was demonstrated by virus indexing. Only 68 showed some resistance. The other 383 were found susceptible, with 77 of them expressing systemic necrosis, the remainder showing mosaic symptoms

MUNGE PROFMUKUNYAD. "Kedera, C.J., D.M. Mukunya and S.O. Keya, 1988. Survival of Rhizobium leguminosarum bv. Phaseoli in contact with Captan.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1988. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1988. Safe and Effective use of pesticides. Paper presented at the PCAK/GIFP workshop on responsible and effective Crop Protection held in Nairobi, Kenya. 11 .". In: Proceedings of 1st Plant Pathology Society of Kenya Conference, 23-24 Nov. 1989. Nairobi, Kenya. 15P. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1988. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. and C. Muinamia, 1988. Rational use of pesticides in Horticulture with special emphasis on Kenya. ACTA HORT. 218: 261 .". In: Proceedings of 1st Plant Pathology Society of Kenya Conference, 23-24 Nov. 1989. Nairobi, Kenya. 15P. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1988. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mutitu, E.W., D.M. Mukunya and S.O. Keya, 1988. Effect of antagonistic bacteria isolated from soil organic amendments on Fusarium oxyysporum Schl. In culture. Abstract 5th International congress on Plant Pathology, Kyoto, Japan.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1988. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mwang.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1988. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Njeru, R.W., D.M. Mukunya and E.M. Gathuru, 1988. Etiology and chemical control of Cercospora leaf spot of the ornamental bellies of Ireland (Molucella leavis L.) Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4 .". In: Proceedings of 1st Plant Pathology Society of Kenya Conference, 23-24 Nov. 1989. Nairobi, Kenya. 15P. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1988. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1987
MUNGE PROFMUKUNYAD. "Gathuru, E.M. and D.M. Mukunya and R.A. Buruchara, 1987. Diseases of crop plants in small scale farms of Embu Agro-ecozone I-IV and farmers awareness on disease control methods. In integrated Crop Protection for Small Scale Farmers in Eastern Africa. Comm.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1987. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Kimani, V.W. and D.M. Mukunya, 1987. Control of pesticides residues in food. Paper presented at the National Food Control Seminar, Kenya Bureau of Standards. 6-9th Oct. 1987. Nairobi, Kenya.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1987. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya D.M. 1987. Pesticides in our environment. Presented at the Regional Workshop on Environmental Protection for the Greenbelt Movement held at the college of Education and External Studies, Kikuyu, University of Nairobi, Kenya. 11p.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1987. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya D.M. 1987. Pesticides in our environment. Presented at the Regional Workshop on Environmental Protection for the Greenbelt Movement held at the college of Education and External Studies, Kikuyu, University of Nairobi, Kenya. 11p.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1987. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Omunyin, M.E., E.M. Gathuru and D.M. Mukunya, 1987. Reactions of cultivars of beans (Phaseolus vulgaris L.) to bean common mosaic virus (BCMV). Trop. Agric. (Trinidad) 65 (2): 166 .". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1987. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1986
Mukunya DM, Gatharu EM, Omunyin ME. "Strains of BCMV and their interaction with I-gene bean varieties.". 1986.
MUNGE PROFMUKUNYAD. "Bondole wa Mbula, E.M. Gathuru, 1986. Malakisi tobacco necrosis virus. Proceeding of the symposium on viral diseases in Africa held in Nairobi, Kenya. O.A.U. Scientific and Technical Res. Council Publication.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1986. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mathangya, P.M., D.M. Mukunya and E.M. Gathuru, 1986. Aetiology and sources of resistance to common blight (Xanthomonas campestris pv. Phaseolus (Smith, 1987). Dye,1978, of beans (phaseolus vulgaris L. ) in Kenya. Kenya Jour. Of Science Series B. 7 (2): 2.". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1986. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Omunyin, M.E. Gathuru and D.M. Mukunya, 1986. Las Cepas, del BCMCY. Su. Interaction Con Variedades de Frijol Con el Gene 1. Hojas de Frijol 8 (3).". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1986. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1985
MUNGE PROFMUKUNYAD. "Buruchara, R.A., E.M.Gathuru and D.M. Mukunya, 1985. Disease progress of angular leaf spot caused by Isariopsis griseola sacc. And it implications on resistance of some bean (Phaseolus vulgaris L.) cultivars. ACTA HORTICULATURAE 218: 321 .". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1985. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Buruchara, R.A., E.M.Gathuru and D.M. Mukunya, 1985. Disease progress of angular leaf spot caused by Isariopsis griseola sacc. And it implications on resistance of some bean (Phaseolus vulgaris L.) cultivars. ACTA HORTICULATURAE 218: 321 .". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1985. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mutitu, E.W., D.M. Mukunya and S.O. Keya, 1985, Biological control of Fusarium yellow on beans caused by Fusarium oxysporum Schl. F.sp phaseolus Kendrick and Snyder using organic amendments. ACTA HORT. 218:267 .". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1985. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1984
MUNGE PROFMUKUNYAD. "Nyangeri, J.P., E.M. Gathuru and D.M. Mukunya, 1984. Effect of latent infection on the spread of Bacterial wilt of Potatoes in Kenya. Trop. Pest management 30 (2): 163 .". In: Proceedings of the 1st Symposium of the Crop Science Society of Kenya held on 4-8th July 1988. Nairobi, Kenya. 15 p. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1984. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1983
Muigai SGS;, Njuguna SK;, Mukunya DM;, Ngugi DN. "Current bean research programmes in Kenya.".; 1983.
1982
Kinyua GK;, Mukunya DM;, Van Breukelen EM. "Studies on genetic resistance of beans to Pseudomonas phaseolicola in Kenya."; 1982.
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1982. Development of crop varieties for disease resistance.". In: Proceedings of the third FAO/SIDA seminar on . Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1982. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1982. UNDP/FAO Evaluation study on National Agricultural Research, Kenya 195 +35 Annex tables, FAO, ROME.". In: Proceedings of the Workshop on root and Tuber crops held in Burundi. IITA. Ibadan, Nigeria. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1982. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. et al. 1982. Citrus greening disease in Kenya and recommendations for its control. Ministry of Agriculture Publication. 128 p.". In: Proceedings of the Workshop on root and Tuber crops held in Burundi. IITA. Ibadan, Nigeria. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1982. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Onyango, D. and D.M. Mukunya. 1982. Bacterial blight of cassava, Xanthomonas manihotis in Kenya.". In: Proceedings of the Workshop on root and Tuber crops held in Burundi. IITA. Ibadan, Nigeria. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1982. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1981
Mukunya DM;, Muthangya PM;, Esele JPE. "Bacterial Blights Of Beans (phaseolus Vulgaris) In Kenya.".; 1981.
MUNGE PROFMUKUNYAD. "Kinyua, G.K., D.M. Mukunya and E.M. Van Breukelen, 1981. Variability in isolates of Pseudomonas phaseolicola (Burk) Dowson in Kenya and genetic studies on resistance in dry food beans.". In: Proceedings of the 5th International Conf. Oin Phytopathogenic Bacteria. Aug. 1981, CIAT, Colombia. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1981. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M., P.M. Muthangya and J.P.E. Esele 1981. Bacterial blights of beans (Phaseolus vulgaris) in Kenya.". In: Proceedings of the 5th International Congress on Phytopathologenic Bacteria. August 1981. CIAT. Colombia. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1981. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1980
"Cowpea research in Kenya." Department of Land Resource Management and Agricultural Technology (LARMAT). 1980;1980.
MUNGE PROFMUKUNYAD. "Njuguna, S.K., A.M.M. Ndegwa, H.A. Van Rheenen and D.M. Mukunya, 1980. Bean production in Kenya. Workshop on potentials for Bean production in Eastern Africa, Malawi, March, 1980. In potentials for Bean production in Eastern Africa. Published 1981 .". In: Proceedings of the 5th International Conf. Oin Phytopathogenic Bacteria. Aug. 1981, CIAT, Colombia. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1980. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1979
MUNGE PROFMUKUNYAD. "Keya S.O. and D.M. Mukunya, 1979. The influence of phosphorus and molybdenum application on modulation of Canadian Wonder bean variety.". In: Proceedings of Grain Legume Symposium held in Nairobi, Kenya, October 1979. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1979. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Keya, S.O., Mukunya, D.M., Ngugi, D.N. and Waithaka, K. 1979. Suggestions for modification of curriculum in Agricultural institutes to make them more effective for ruraldevelopment. In Seminar Report of the international Association of agriculture Student.". In: The proceedings of a workshop held at Kahuhui, Maui, Hawaii, Jan 15 . Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1979. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Keya, S.O., Ssali, H. Mukunya, D.M., Muruli, B.I. and Onim, J.F. 1979. Legume research at the University of Nairobi, in planning International Network of Legume inoculation trials.". In: The proceedings of a workshop held at Kahuhui, Maui, Hawaii, Jan 15 . Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1979. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. and S.O. Keya, 1979. Effects of seeds borne innoculum on disease development and yields of Canadian Wonder bean variety in Kenya.". In: Proceedings grain Legume Symposium held in Nairobi, Kenya. October, 1979. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1979. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mutitu, E.W. and D.M. Mukunya, 1979. Epidemiology and control of bean scab caused by Elsinoe Phaseolus Jenkins in Kenya.". In: Proceedings of the grain Legume Symposium held in Nairobi, Oct. 1979. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1979. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1978
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1978. Diseases affecting cowpeas in Kenya. Cowpeas Improvement Programme in Kenya. First Annual Report 61 .". In: The proceedings of a workshop held at Kahuhui, Maui, Hawaii, Jan 15 . Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1978. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. and S.O. Keya, 1978. Yield performance and selection of resistance in beans (Phaseolus vulgaris L.) to common disease in Kenya. In E.A. Agric. For. J. 43:4-8.". In: The proceedings of a workshop held at Kahuhui, Maui, Hawaii, Jan 15 . Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1978. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1977
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1977. Development of horizontal resistance in beans.". In: Presented at the FAO/IITA Crop Loss Horizontal Resistance Workshop. Ibadan, Nigeria October, 1977. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1977. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1976
Mukunya DM. "Agriculture."; 1976.
Mukunya DM. "Grain Storage."; 1976.
MUNGE PROFMUKUNYAD. "Mukunya, D. M. 1976. Development disease resistance in local beans (Phaseolus vulgaris L.) in Kenya.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1976. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1976. Agriculture .". In: Presented at the FAO/IITA Crop Loss Horizontal Resistance Workshop. Ibadan, Nigeria October, 1977. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1976. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1976. Grain Storage, A chapter in D. Ngugi et al. East Africa Agriculture. A text book for schools. Macmillan Publishers Ltd. P. 76 .". In: Presented at the FAO/IITA Crop Loss Horizontal Resistance Workshop. Ibadan, Nigeria October, 1977. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1976. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. and S.O. Keya, 1976. Phaseolus bean production in East Africa. A review paper prepared for publication in the Handbook of Agriculture in East Africa Publishing House, Nairobi 81 p.". In: Presented at the FAO/IITA Crop Loss Horizontal Resistance Workshop. Ibadan, Nigeria October, 1977. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1976. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1975
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1975. Sources of resistance to bean anthracnose and bean rust in Kenya local dry beans. Ann. Rept. Improvement Co-op.18:49-51.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1975. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1975. The occurrence in Kenya of a maize leaf blight caused by Phyllosticta maydis. Plant Disease Rept. 59:164-168.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1975. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M., C.W. Boothroyd and C.O. Grogan 1975. Genetic nature of resistance in corn to yellow leaf blight. Crop Science 15:495-501.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1975. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1974
Mukunya DM. "Bean Diseases In Kenya.".; 1974.
MUNGE PROFMUKUNYAD. "Mukunya, D.M. 1974. Bean diseases in Kenya. Ann. Rept. Bean Improvement Coop. 17; 57-59.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1974. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1973
MUNGE PROFMUKUNYAD. "Mukunya, D.M. and C.W. Boothroyd 1973. Mycosphaerella zea-mays sp.n, the sexual of Phyllostica maydis. Phytopathology 63:529-532.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1973. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
MUNGE PROFMUKUNYAD. "Mukunya, D.M. and C.W. Boothroyd 1973. Survival and spore dissertation of Mycosphaerella zeamaydis. Phytopathology 63:568.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1973. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1972
MUNGE PROFMUKUNYAD. "Yoder, O and D.M.Mukunya, 1972. A host specific toxin metabolite produced by Phyllostica maydis. Phytopathology 62:799.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1972. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43
1970
MUNGE PROFMUKUNYAD. "Mukunya, D.M. and C.W. Boothroyd, 1970. Phyllosticta leaf spot and tests for resistance to this disease. Phytopathology 60:577.". In: A seminar paper presented to the members of the institute of Botany and Physiology. July, 1976. Shangai, People. Plant Molecular Biology Reporter Vol. 27, pp. 79-85.; 1970. Abstract
The gene Q13L coding for the Capripoxvirus group specific structural protein P32 was expressed in Escherichia coli using plasmid pGEX-2T as a fusion protein with glutathione-s-transferase and purified on glutathione sepharose affinity chromatography column. The protein was then employed for diagnosis of sheeppox, goatpox and lumpyskin disease, by a latex agglutination test (LAT) using the purified P32 antigen and guinea pig detector antiserum raised against the P32 antigen. The LAT and virus neutralization test (VNT) were used to screen one hundred livestock field sera for antibodies to Capripoxvirus, in comparison the LAT was simpler, rapid and 23% more sensitive than the VNT. In addition the LAT was found to be specific for Carpripoxvirus because it did not pick antibodies to Orthopoxvirus and Parapoxvirus. The LA test can be taken for a simple and quick diagnostic tool for primary screening of Carpripoxvirus infection and will reduce the reliance of diagnostic laboratories on tissue culture facilities. Keywords: Carpripox, latex agglutination test, attachment gene J. Trop. Microbiol. Biotechnol. Vol. 3 (2) 2007: pp. 36-43

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