Identification and purification of specific Penicillium marneffei antigens and their recognition by human immune sera
Disseminated infection with the dimorphic pathogenic fungus Penicillium marneffei is increasingly seen among patients with AIDS in southeast Asian countries. Previous studies have demonstrated the presence of humoral immune responses to this fungus in patient sera; we have confirmed this work using...
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Veröffentlicht in: | Journal of clinical microbiology 1998-04, Vol.36 (4), p.949-954 |
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description | Disseminated infection with the dimorphic pathogenic fungus Penicillium marneffei is increasingly seen among patients with AIDS in southeast Asian countries. Previous studies have demonstrated the presence of humoral immune responses to this fungus in patient sera; we have confirmed this work using sera from P. marneffei-infected patients (n = 21) to develop Western blots of P. marneffei cytoplasmic yeast antigen (CYA). P. marneffei CYA was then partially purified by liquid isoelectric focusing, and fractions were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting. Immunoenzyme development of the Western blots with pooled sera from patients with P. marneffei infection and with pooled sera from patients with aspergillosis (n = 20), candidiasis (n = 10), cryptococcosis (n = 9), and histoplasmosis (n = 11) revealed three antigens with relative molecular masses of 61, 54, and 50 kDa. These antigens were specifically recognized by the pooled sera from the P. marneffei-infected patients. The 61- and 54-kDa antigens were subsequently purified to homogeneity by preparative gel electrophoresis, and the 50-kDa antigen was partially purified by the same technique. N-terminal amino acid sequencing revealed that the 61-kDa antigen had a strong homology (87% identity) with the antioxidant enzyme catalase. The three antigens were then subjected to SDS-PAGE and Western blotting and to immunoenzyme development with individual patient sera; sera from 86% of P. marneffei-infected patients recognized the 61-kDa antigen, sera from 71% recognized the 54-kDa antigen, and sera from 48% recognized the 50-kDa antigen. These specifically recognized antigens are the first to be purified from P. marneffei and can be used either singly or in combination to detect antibody responses in a large percentage of individuals infected with P. marneffei. |
doi_str_mv | 10.1128/jcm.36.4.949-954.1998 |
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J ; VANITTANAKOM, N ; UNGPAKORN, R ; EVANS, E. G. V ; SIRISANTHANA, T ; HAY, R. J</creator><creatorcontrib>JEAVONS, L ; HAMILTON, A. J ; VANITTANAKOM, N ; UNGPAKORN, R ; EVANS, E. G. V ; SIRISANTHANA, T ; HAY, R. J</creatorcontrib><description>Disseminated infection with the dimorphic pathogenic fungus Penicillium marneffei is increasingly seen among patients with AIDS in southeast Asian countries. Previous studies have demonstrated the presence of humoral immune responses to this fungus in patient sera; we have confirmed this work using sera from P. marneffei-infected patients (n = 21) to develop Western blots of P. marneffei cytoplasmic yeast antigen (CYA). P. marneffei CYA was then partially purified by liquid isoelectric focusing, and fractions were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting. Immunoenzyme development of the Western blots with pooled sera from patients with P. marneffei infection and with pooled sera from patients with aspergillosis (n = 20), candidiasis (n = 10), cryptococcosis (n = 9), and histoplasmosis (n = 11) revealed three antigens with relative molecular masses of 61, 54, and 50 kDa. These antigens were specifically recognized by the pooled sera from the P. marneffei-infected patients. The 61- and 54-kDa antigens were subsequently purified to homogeneity by preparative gel electrophoresis, and the 50-kDa antigen was partially purified by the same technique. N-terminal amino acid sequencing revealed that the 61-kDa antigen had a strong homology (87% identity) with the antioxidant enzyme catalase. The three antigens were then subjected to SDS-PAGE and Western blotting and to immunoenzyme development with individual patient sera; sera from 86% of P. marneffei-infected patients recognized the 61-kDa antigen, sera from 71% recognized the 54-kDa antigen, and sera from 48% recognized the 50-kDa antigen. 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J</creatorcontrib><creatorcontrib>VANITTANAKOM, N</creatorcontrib><creatorcontrib>UNGPAKORN, R</creatorcontrib><creatorcontrib>EVANS, E. G. V</creatorcontrib><creatorcontrib>SIRISANTHANA, T</creatorcontrib><creatorcontrib>HAY, R. J</creatorcontrib><title>Identification and purification of specific Penicillium marneffei antigens and their recognition by human immune sera</title><title>Journal of clinical microbiology</title><addtitle>J Clin Microbiol</addtitle><description>Disseminated infection with the dimorphic pathogenic fungus Penicillium marneffei is increasingly seen among patients with AIDS in southeast Asian countries. Previous studies have demonstrated the presence of humoral immune responses to this fungus in patient sera; we have confirmed this work using sera from P. marneffei-infected patients (n = 21) to develop Western blots of P. marneffei cytoplasmic yeast antigen (CYA). P. marneffei CYA was then partially purified by liquid isoelectric focusing, and fractions were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting. Immunoenzyme development of the Western blots with pooled sera from patients with P. marneffei infection and with pooled sera from patients with aspergillosis (n = 20), candidiasis (n = 10), cryptococcosis (n = 9), and histoplasmosis (n = 11) revealed three antigens with relative molecular masses of 61, 54, and 50 kDa. These antigens were specifically recognized by the pooled sera from the P. marneffei-infected patients. The 61- and 54-kDa antigens were subsequently purified to homogeneity by preparative gel electrophoresis, and the 50-kDa antigen was partially purified by the same technique. N-terminal amino acid sequencing revealed that the 61-kDa antigen had a strong homology (87% identity) with the antioxidant enzyme catalase. The three antigens were then subjected to SDS-PAGE and Western blotting and to immunoenzyme development with individual patient sera; sera from 86% of P. marneffei-infected patients recognized the 61-kDa antigen, sera from 71% recognized the 54-kDa antigen, and sera from 48% recognized the 50-kDa antigen. These specifically recognized antigens are the first to be purified from P. marneffei and can be used either singly or in combination to detect antibody responses in a large percentage of individuals infected with P. marneffei.</description><subject>Antigens, Fungal - analysis</subject><subject>Antigens, Fungal - immunology</subject><subject>Antigens, Fungal - isolation & purification</subject><subject>Biological and medical sciences</subject><subject>Human mycoses</subject><subject>Humans</subject><subject>Immune Sera - immunology</subject><subject>Immunoblotting</subject><subject>Immunoenzyme Techniques</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Molecular Weight</subject><subject>Mycology</subject><subject>Mycoses</subject><subject>Mycotic sepsis</subject><subject>Penicillium - immunology</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU9v1DAQxS0EKkvhI1TyAXFL8P_YBw5oVaCoqD2AxM3yOuNdV4mz2AlSv3297Wqhp5Hmvd_M2A-hC0paSpn-eOfHlqtWtEaYxkjRUmP0C7SixOhGKfL7JVoRYmRDKe9eozel3BFChZDyDJ1VPzNUrNBy1UOaY4jezXFK2KUe75f8rzEFXPbgDw18Cyn6OAxxGfHocoIQIFZkjltI5ZGddxAzzuCnbYqPAzb3eLeMLuE4jksCXCC7t-hVcEOBd8d6jn59ufy5_tZc33y9Wn--brzgYm6c1kFtNtAzRZjpaRAggyCC8M6TTmvtnQpEUQah96bvCZWKGukBOqkcZfwcfXqau182I_S-PjW7we5zrOff28lF-1xJcWe3019LiVBKVf7Dkc_TnwXKbMdYPAyDSzAtxXam05QJXo3yyejzVEqGcNpBiT3EZb-vf1iurLA1Llu_3x7iqtzF_weeqGM-VX9_1F3xbgjZJR_LycYYl6aT_AHJNKJc</recordid><startdate>19980401</startdate><enddate>19980401</enddate><creator>JEAVONS, L</creator><creator>HAMILTON, A. 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J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-a88f6bbed26029d1f4e5f404037c07888ca6f0612efdc9dd0156195cee756a123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Antigens, Fungal - analysis</topic><topic>Antigens, Fungal - immunology</topic><topic>Antigens, Fungal - isolation & purification</topic><topic>Biological and medical sciences</topic><topic>Human mycoses</topic><topic>Humans</topic><topic>Immune Sera - immunology</topic><topic>Immunoblotting</topic><topic>Immunoenzyme Techniques</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Molecular Weight</topic><topic>Mycology</topic><topic>Mycoses</topic><topic>Mycotic sepsis</topic><topic>Penicillium - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>JEAVONS, L</creatorcontrib><creatorcontrib>HAMILTON, A. J</creatorcontrib><creatorcontrib>VANITTANAKOM, N</creatorcontrib><creatorcontrib>UNGPAKORN, R</creatorcontrib><creatorcontrib>EVANS, E. G. V</creatorcontrib><creatorcontrib>SIRISANTHANA, T</creatorcontrib><creatorcontrib>HAY, R. J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>JEAVONS, L</au><au>HAMILTON, A. J</au><au>VANITTANAKOM, N</au><au>UNGPAKORN, R</au><au>EVANS, E. G. V</au><au>SIRISANTHANA, T</au><au>HAY, R. J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and purification of specific Penicillium marneffei antigens and their recognition by human immune sera</atitle><jtitle>Journal of clinical microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>1998-04-01</date><risdate>1998</risdate><volume>36</volume><issue>4</issue><spage>949</spage><epage>954</epage><pages>949-954</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><coden>JCMIDW</coden><abstract>Disseminated infection with the dimorphic pathogenic fungus Penicillium marneffei is increasingly seen among patients with AIDS in southeast Asian countries. Previous studies have demonstrated the presence of humoral immune responses to this fungus in patient sera; we have confirmed this work using sera from P. marneffei-infected patients (n = 21) to develop Western blots of P. marneffei cytoplasmic yeast antigen (CYA). P. marneffei CYA was then partially purified by liquid isoelectric focusing, and fractions were subjected to sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Western blotting. Immunoenzyme development of the Western blots with pooled sera from patients with P. marneffei infection and with pooled sera from patients with aspergillosis (n = 20), candidiasis (n = 10), cryptococcosis (n = 9), and histoplasmosis (n = 11) revealed three antigens with relative molecular masses of 61, 54, and 50 kDa. These antigens were specifically recognized by the pooled sera from the P. marneffei-infected patients. The 61- and 54-kDa antigens were subsequently purified to homogeneity by preparative gel electrophoresis, and the 50-kDa antigen was partially purified by the same technique. N-terminal amino acid sequencing revealed that the 61-kDa antigen had a strong homology (87% identity) with the antioxidant enzyme catalase. The three antigens were then subjected to SDS-PAGE and Western blotting and to immunoenzyme development with individual patient sera; sera from 86% of P. marneffei-infected patients recognized the 61-kDa antigen, sera from 71% recognized the 54-kDa antigen, and sera from 48% recognized the 50-kDa antigen. These specifically recognized antigens are the first to be purified from P. marneffei and can be used either singly or in combination to detect antibody responses in a large percentage of individuals infected with P. marneffei.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>9542914</pmid><doi>10.1128/jcm.36.4.949-954.1998</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, Fungal - analysis Antigens, Fungal - immunology Antigens, Fungal - isolation & purification Biological and medical sciences Human mycoses Humans Immune Sera - immunology Immunoblotting Immunoenzyme Techniques Infectious diseases Medical sciences Molecular Weight Mycology Mycoses Mycotic sepsis Penicillium - immunology |
title | Identification and purification of specific Penicillium marneffei antigens and their recognition by human immune sera |
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