Purification of Enterocytozoon bieneusi from Stools and Production of Specific Antibodies
Enterocytozoon bieneusi is clinically the most significant of the microsporidia in humans, causing chronic diarrhea wasting and cholangitis in individuals with human immunodeficiency virus infection and AIDS. Little progress on this infection has been made because of the inability to propagate E. bi...
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Veröffentlicht in: | Journal of Clinical Microbiology 2005, Vol.43 (1), p.387-392 |
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description | Enterocytozoon bieneusi is clinically the most significant of the microsporidia in humans, causing chronic diarrhea wasting and cholangitis in individuals with human immunodeficiency virus infection and AIDS. Little progress on this infection has been made because of the inability to propagate E. bieneusi in vitro and in vivo, which limits the source of parasite spores to the stools of infected human patients. Given the size and shape of the E. bieneusi spores (1.1 to 1.6 by 0.7 to 1.0 [micro]m) and the lack of specific immune reagents, the identification and purification of large quantities of spores from feces are technically challenging. Consequently, diagnosis relies entirely on PCR, a labor-intensive approach that requires highly skilled personnel. We describe a method for the purification of E. bieneusi spores from human stools and the production of rabbit-specific antisera. Spores were purified by a combination of isopycnic Percoll gradient centrifugation and continuous sucrose gradient centrifugation. Specific polyclonal antibodies raised in mice and rabbits reacted by indirect immunofluorescence with E. bieneusi but not with Encephalitozoon spp., Candida albicans, Staphylococcus aureus, Escherichia coli, or other forms present in human stools. |
doi_str_mv | 10.1128/JCM.43.1.387-392.2005 |
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Little progress on this infection has been made because of the inability to propagate E. bieneusi in vitro and in vivo, which limits the source of parasite spores to the stools of infected human patients. Given the size and shape of the E. bieneusi spores (1.1 to 1.6 by 0.7 to 1.0 [micro]m) and the lack of specific immune reagents, the identification and purification of large quantities of spores from feces are technically challenging. Consequently, diagnosis relies entirely on PCR, a labor-intensive approach that requires highly skilled personnel. We describe a method for the purification of E. bieneusi spores from human stools and the production of rabbit-specific antisera. Spores were purified by a combination of isopycnic Percoll gradient centrifugation and continuous sucrose gradient centrifugation. Specific polyclonal antibodies raised in mice and rabbits reacted by indirect immunofluorescence with E. bieneusi but not with Encephalitozoon spp., Candida albicans, Staphylococcus aureus, Escherichia coli, or other forms present in human stools.</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/JCM.43.1.387-392.2005</identifier><identifier>PMID: 15634999</identifier><identifier>CODEN: JCMIDW</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Antibodies, Protozoan - biosynthesis ; Antibodies, Protozoan - blood ; Antibodies, Protozoan - immunology ; Antibody Specificity ; Biological and medical sciences ; Candida albicans ; Centrifugation, Density Gradient - methods ; Encephalitozoon ; Enterocytozoon - immunology ; Enterocytozoon - isolation & purification ; Enterocytozoon - physiology ; Enterocytozoon bieneusi ; Escherichia coli ; Feces - parasitology ; Fundamental and applied biological sciences. Psychology ; Human immunodeficiency virus ; Humans ; Infectious diseases ; Medical sciences ; Mice ; Microbiology ; Microsporidia ; Microsporidiosis - parasitology ; Parasitology ; Rabbits ; Spores, Protozoan - immunology ; Spores, Protozoan - isolation & purification ; Staphylococcus aureus</subject><ispartof>Journal of Clinical Microbiology, 2005, Vol.43 (1), p.387-392</ispartof><rights>2005 INIST-CNRS</rights><rights>Copyright © 2005, American Society for Microbiology 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-5b3ff44af696c231bc90b03ab30fcd7946f0c38cb0d27bd6637277b8f77b527b3</citedby><cites>FETCH-LOGICAL-c518t-5b3ff44af696c231bc90b03ab30fcd7946f0c38cb0d27bd6637277b8f77b527b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC540125/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC540125/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,4010,27900,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16561188$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15634999$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sheoran, Abhineet S</creatorcontrib><creatorcontrib>Feng, Xiaochuan</creatorcontrib><creatorcontrib>Kitaka, Sabrina</creatorcontrib><creatorcontrib>Green, Linda</creatorcontrib><creatorcontrib>Pearson, Christine</creatorcontrib><creatorcontrib>Didier, Elizabeth S</creatorcontrib><creatorcontrib>Chapman, Susan</creatorcontrib><creatorcontrib>Tumwine, James K</creatorcontrib><creatorcontrib>Tzipori, Saul</creatorcontrib><title>Purification of Enterocytozoon bieneusi from Stools and Production of Specific Antibodies</title><title>Journal of Clinical Microbiology</title><addtitle>J Clin Microbiol</addtitle><description>Enterocytozoon bieneusi is clinically the most significant of the microsporidia in humans, causing chronic diarrhea wasting and cholangitis in individuals with human immunodeficiency virus infection and AIDS. Little progress on this infection has been made because of the inability to propagate E. bieneusi in vitro and in vivo, which limits the source of parasite spores to the stools of infected human patients. Given the size and shape of the E. bieneusi spores (1.1 to 1.6 by 0.7 to 1.0 [micro]m) and the lack of specific immune reagents, the identification and purification of large quantities of spores from feces are technically challenging. Consequently, diagnosis relies entirely on PCR, a labor-intensive approach that requires highly skilled personnel. We describe a method for the purification of E. bieneusi spores from human stools and the production of rabbit-specific antisera. Spores were purified by a combination of isopycnic Percoll gradient centrifugation and continuous sucrose gradient centrifugation. Specific polyclonal antibodies raised in mice and rabbits reacted by indirect immunofluorescence with E. bieneusi but not with Encephalitozoon spp., Candida albicans, Staphylococcus aureus, Escherichia coli, or other forms present in human stools.</description><subject>Animals</subject><subject>Antibodies, Protozoan - biosynthesis</subject><subject>Antibodies, Protozoan - blood</subject><subject>Antibodies, Protozoan - immunology</subject><subject>Antibody Specificity</subject><subject>Biological and medical sciences</subject><subject>Candida albicans</subject><subject>Centrifugation, Density Gradient - methods</subject><subject>Encephalitozoon</subject><subject>Enterocytozoon - immunology</subject><subject>Enterocytozoon - isolation & purification</subject><subject>Enterocytozoon - physiology</subject><subject>Enterocytozoon bieneusi</subject><subject>Escherichia coli</subject><subject>Feces - parasitology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Microsporidia</subject><subject>Microsporidiosis - parasitology</subject><subject>Parasitology</subject><subject>Rabbits</subject><subject>Spores, Protozoan - immunology</subject><subject>Spores, Protozoan - isolation & purification</subject><subject>Staphylococcus aureus</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkktv1DAUhS0EokPhJwDZwC6Db_yKFyyqUXmpiEpDJVhZtmPPuEriqZ2Ayq_HoxlaWLG5lq6_c-61jhF6DngJ0LRvPq0-LylZwpK0oiayWTYYswdoAVi2Nef420O0wFiyGoCIE_Qk52uMgVLGHqMTYJxQKeUCfb-cU_DB6inEsYq-Oh8nl6K9neKvWDomuNHNOVQ-xaFaTzH2udJjV12m2M32j2q9c3ZvU52NUzCxCy4_RY-87rN7djxP0dW786-rD_XFl_cfV2cXtWXQTjUzxHtKteeS24aAsRIbTLQh2NtOSMo9tqS1BneNMB3nRDRCmNaXwkqHnKK3B9_dbAbXWTdOSfdql8Kg062KOqh_b8awVZv4QzGKoWFF__qoT_FmdnlSQ8jW9b0eXZyz4oJQ3OD2vyCIFkAIKCA7gDbFnJPzd8sAVvvwVAlPUaJAlfBUCU_twyu6F3-_5F51TKsAr46Azlb3PunRhnzPccYB2v2m1YHbhs32Z0hO6TyoazvcDS3IywPidVR6k4rN1brBQMqfkaIU8hvZ2bkb</recordid><startdate>2005</startdate><enddate>2005</enddate><creator>Sheoran, Abhineet S</creator><creator>Feng, Xiaochuan</creator><creator>Kitaka, Sabrina</creator><creator>Green, Linda</creator><creator>Pearson, Christine</creator><creator>Didier, Elizabeth S</creator><creator>Chapman, Susan</creator><creator>Tumwine, James K</creator><creator>Tzipori, Saul</creator><general>American Society for Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2005</creationdate><title>Purification of Enterocytozoon bieneusi from Stools and Production of Specific Antibodies</title><author>Sheoran, Abhineet S ; Feng, Xiaochuan ; Kitaka, Sabrina ; Green, Linda ; Pearson, Christine ; Didier, Elizabeth S ; Chapman, Susan ; Tumwine, James K ; Tzipori, Saul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c518t-5b3ff44af696c231bc90b03ab30fcd7946f0c38cb0d27bd6637277b8f77b527b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Antibodies, Protozoan - biosynthesis</topic><topic>Antibodies, Protozoan - blood</topic><topic>Antibodies, Protozoan - immunology</topic><topic>Antibody Specificity</topic><topic>Biological and medical sciences</topic><topic>Candida albicans</topic><topic>Centrifugation, Density Gradient - methods</topic><topic>Encephalitozoon</topic><topic>Enterocytozoon - immunology</topic><topic>Enterocytozoon - isolation & purification</topic><topic>Enterocytozoon - physiology</topic><topic>Enterocytozoon bieneusi</topic><topic>Escherichia coli</topic><topic>Feces - parasitology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Microsporidia</topic><topic>Microsporidiosis - parasitology</topic><topic>Parasitology</topic><topic>Rabbits</topic><topic>Spores, Protozoan - immunology</topic><topic>Spores, Protozoan - isolation & purification</topic><topic>Staphylococcus aureus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheoran, Abhineet S</creatorcontrib><creatorcontrib>Feng, Xiaochuan</creatorcontrib><creatorcontrib>Kitaka, Sabrina</creatorcontrib><creatorcontrib>Green, Linda</creatorcontrib><creatorcontrib>Pearson, Christine</creatorcontrib><creatorcontrib>Didier, Elizabeth S</creatorcontrib><creatorcontrib>Chapman, Susan</creatorcontrib><creatorcontrib>Tumwine, James K</creatorcontrib><creatorcontrib>Tzipori, Saul</creatorcontrib><collection>AGRIS</collection><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>Algology Mycology and Protozoology Abstracts (Microbiology C)</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>Sheoran, Abhineet S</au><au>Feng, Xiaochuan</au><au>Kitaka, Sabrina</au><au>Green, Linda</au><au>Pearson, Christine</au><au>Didier, Elizabeth S</au><au>Chapman, Susan</au><au>Tumwine, James K</au><au>Tzipori, Saul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Purification of Enterocytozoon bieneusi from Stools and Production of Specific Antibodies</atitle><jtitle>Journal of Clinical Microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>2005</date><risdate>2005</risdate><volume>43</volume><issue>1</issue><spage>387</spage><epage>392</epage><pages>387-392</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><coden>JCMIDW</coden><abstract>Enterocytozoon bieneusi is clinically the most significant of the microsporidia in humans, causing chronic diarrhea wasting and cholangitis in individuals with human immunodeficiency virus infection and AIDS. Little progress on this infection has been made because of the inability to propagate E. bieneusi in vitro and in vivo, which limits the source of parasite spores to the stools of infected human patients. Given the size and shape of the E. bieneusi spores (1.1 to 1.6 by 0.7 to 1.0 [micro]m) and the lack of specific immune reagents, the identification and purification of large quantities of spores from feces are technically challenging. Consequently, diagnosis relies entirely on PCR, a labor-intensive approach that requires highly skilled personnel. We describe a method for the purification of E. bieneusi spores from human stools and the production of rabbit-specific antisera. Spores were purified by a combination of isopycnic Percoll gradient centrifugation and continuous sucrose gradient centrifugation. Specific polyclonal antibodies raised in mice and rabbits reacted by indirect immunofluorescence with E. bieneusi but not with Encephalitozoon spp., Candida albicans, Staphylococcus aureus, Escherichia coli, or other forms present in human stools.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>15634999</pmid><doi>10.1128/JCM.43.1.387-392.2005</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antibodies, Protozoan - biosynthesis Antibodies, Protozoan - blood Antibodies, Protozoan - immunology Antibody Specificity Biological and medical sciences Candida albicans Centrifugation, Density Gradient - methods Encephalitozoon Enterocytozoon - immunology Enterocytozoon - isolation & purification Enterocytozoon - physiology Enterocytozoon bieneusi Escherichia coli Feces - parasitology Fundamental and applied biological sciences. Psychology Human immunodeficiency virus Humans Infectious diseases Medical sciences Mice Microbiology Microsporidia Microsporidiosis - parasitology Parasitology Rabbits Spores, Protozoan - immunology Spores, Protozoan - isolation & purification Staphylococcus aureus |
title | Purification of Enterocytozoon bieneusi from Stools and Production of Specific Antibodies |
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