Antigenic, morphologic, and molecular characterization of new Ehrlichia risticii isolates
Ehrlichia risticii causes an acute infectious disease in horses called Potomac horse fever. To investigate the biological diversity of E. risticii organisms, nine E. risticii isolates derived from the peripheral blood monocytes of clinically sick horses in Ohio and Kentucky during the summers of 199...
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Veröffentlicht in: | Journal of Clinical Microbiology 1994-12, Vol.32 (12), p.3026-3033 |
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description | Ehrlichia risticii causes an acute infectious disease in horses called Potomac horse fever. To investigate the biological diversity of E. risticii organisms, nine E. risticii isolates derived from the peripheral blood monocytes of clinically sick horses in Ohio and Kentucky during the summers of 1991 and 1993 were compared with Illinois and Virginia isolates originally obtained from horses in Maryland in 1984. Seven of the nine isolates (081, 606, 380, 679, As, Co, and Ov) formed large morulae (tightly packed inclusions of ehrlichial organisms). The remaining isolates, including 1984 isolates, were individually dispersed or formed small morulae in the cytoplasm of P388D1 cells. In Western blot (immunoblot) analysis with four equine and one rabbit polyclonal anti-E. risticii sera, these recent E. risticii isolates showed patterns of antigenic proteins distinct from those of the 1984 isolates and could be divided into three groups: (i) 081; (ii) 606, 022, 067, 380, and 679; and (iii) As, Co, and Ov. By indirect fluorescent antibody labeling with two panels of murine anti-E. risticii (Illinois and Maryland isolates) monoclonal antibodies, isolate 081 was not labeled with any of 20 monoclonal antibodies tested. The remaining isolates were not labeled with several monoclonal antibodies. The digestion pattern with one of the restriction enzymes, AvaII, of the PCR-amplified partial 16S rRNA gene of E. risticii from all Kentucky isolates (As, Co, and Ov) was different from that of Illinois, Virginia, and six Ohio isolates. These results indicate the presence of distinct variants of E. risticii which vary significantly in morpbology, antigenic composition, and the base sequence of the 16S rRNA gene |
doi_str_mv | 10.1128/JCM.32.12.3026-3033.1994 |
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(Ohio State University, Columbus, OH.) ; Rikihisa, Y ; Yamamoto, S ; Reed, S ; Crawford, T.B ; Perryman, L.E ; Palmer, G.H</creator><creatorcontrib>Chaichanasiriwithaya, W. (Ohio State University, Columbus, OH.) ; Rikihisa, Y ; Yamamoto, S ; Reed, S ; Crawford, T.B ; Perryman, L.E ; Palmer, G.H</creatorcontrib><description>Ehrlichia risticii causes an acute infectious disease in horses called Potomac horse fever. To investigate the biological diversity of E. risticii organisms, nine E. risticii isolates derived from the peripheral blood monocytes of clinically sick horses in Ohio and Kentucky during the summers of 1991 and 1993 were compared with Illinois and Virginia isolates originally obtained from horses in Maryland in 1984. Seven of the nine isolates (081, 606, 380, 679, As, Co, and Ov) formed large morulae (tightly packed inclusions of ehrlichial organisms). The remaining isolates, including 1984 isolates, were individually dispersed or formed small morulae in the cytoplasm of P388D1 cells. In Western blot (immunoblot) analysis with four equine and one rabbit polyclonal anti-E. risticii sera, these recent E. risticii isolates showed patterns of antigenic proteins distinct from those of the 1984 isolates and could be divided into three groups: (i) 081; (ii) 606, 022, 067, 380, and 679; and (iii) As, Co, and Ov. By indirect fluorescent antibody labeling with two panels of murine anti-E. risticii (Illinois and Maryland isolates) monoclonal antibodies, isolate 081 was not labeled with any of 20 monoclonal antibodies tested. The remaining isolates were not labeled with several monoclonal antibodies. The digestion pattern with one of the restriction enzymes, AvaII, of the PCR-amplified partial 16S rRNA gene of E. risticii from all Kentucky isolates (As, Co, and Ov) was different from that of Illinois, Virginia, and six Ohio isolates. These results indicate the presence of distinct variants of E. risticii which vary significantly in morpbology, antigenic composition, and the base sequence of the 16S rRNA gene</description><identifier>ISSN: 0095-1137</identifier><identifier>EISSN: 1098-660X</identifier><identifier>DOI: 10.1128/JCM.32.12.3026-3033.1994</identifier><identifier>PMID: 7533780</identifier><identifier>CODEN: JCMIDW</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>ADN ; Animals ; ANTIGENE ; ANTIGENOS ; ARN RIBOSOMAL ; ARN RIBOSOMIAL ; BACTERIA ; Bacteriology ; BACTERIOSE ; BACTERIOSIS ; Biological and medical sciences ; CABALLOS ; CHEVAL ; EHRLICHIA ; Ehrlichia - genetics ; Ehrlichia - immunology ; Ehrlichia - ultrastructure ; Ehrlichia risticii ; Ehrlichiosis - microbiology ; Ehrlichiosis - veterinary ; Epidemiology ; Fundamental and applied biological sciences. Psychology ; GENE ; GENES ; Horse Diseases - microbiology ; Horses ; IMMUNOFLUORESCENCE ; IMMUNOLOGIE ; INMUNOFLUORESCENCIA ; INMUNOLOGIA ; KENTUCKY ; MARYLAND ; Mice ; Microbiology ; OHIO ; Polymerase Chain Reaction ; PROTEINAS UNICELULARES ; PROTEINE MICROBIOLOGIQUE ; Rabbits ; RIBOSOMAS ; RIBOSOME ; RNA, Bacterial - genetics ; RNA, Ribosomal, 16S - genetics ; Sequence Analysis, RNA ; TECHNIQUE ANALYTIQUE ; TECNICAS ANALITICAS</subject><ispartof>Journal of Clinical Microbiology, 1994-12, Vol.32 (12), p.3026-3033</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c575t-56526f77e5a80460d272f78c2d119bafaa40c009fb769a71f2ec55857648d7103</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC264219/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC264219/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3348000$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7533780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chaichanasiriwithaya, W. (Ohio State University, Columbus, OH.)</creatorcontrib><creatorcontrib>Rikihisa, Y</creatorcontrib><creatorcontrib>Yamamoto, S</creatorcontrib><creatorcontrib>Reed, S</creatorcontrib><creatorcontrib>Crawford, T.B</creatorcontrib><creatorcontrib>Perryman, L.E</creatorcontrib><creatorcontrib>Palmer, G.H</creatorcontrib><title>Antigenic, morphologic, and molecular characterization of new Ehrlichia risticii isolates</title><title>Journal of Clinical Microbiology</title><addtitle>J Clin Microbiol</addtitle><description>Ehrlichia risticii causes an acute infectious disease in horses called Potomac horse fever. To investigate the biological diversity of E. risticii organisms, nine E. risticii isolates derived from the peripheral blood monocytes of clinically sick horses in Ohio and Kentucky during the summers of 1991 and 1993 were compared with Illinois and Virginia isolates originally obtained from horses in Maryland in 1984. Seven of the nine isolates (081, 606, 380, 679, As, Co, and Ov) formed large morulae (tightly packed inclusions of ehrlichial organisms). The remaining isolates, including 1984 isolates, were individually dispersed or formed small morulae in the cytoplasm of P388D1 cells. In Western blot (immunoblot) analysis with four equine and one rabbit polyclonal anti-E. risticii sera, these recent E. risticii isolates showed patterns of antigenic proteins distinct from those of the 1984 isolates and could be divided into three groups: (i) 081; (ii) 606, 022, 067, 380, and 679; and (iii) As, Co, and Ov. By indirect fluorescent antibody labeling with two panels of murine anti-E. risticii (Illinois and Maryland isolates) monoclonal antibodies, isolate 081 was not labeled with any of 20 monoclonal antibodies tested. The remaining isolates were not labeled with several monoclonal antibodies. The digestion pattern with one of the restriction enzymes, AvaII, of the PCR-amplified partial 16S rRNA gene of E. risticii from all Kentucky isolates (As, Co, and Ov) was different from that of Illinois, Virginia, and six Ohio isolates. These results indicate the presence of distinct variants of E. risticii which vary significantly in morpbology, antigenic composition, and the base sequence of the 16S rRNA gene</description><subject>ADN</subject><subject>Animals</subject><subject>ANTIGENE</subject><subject>ANTIGENOS</subject><subject>ARN RIBOSOMAL</subject><subject>ARN RIBOSOMIAL</subject><subject>BACTERIA</subject><subject>Bacteriology</subject><subject>BACTERIOSE</subject><subject>BACTERIOSIS</subject><subject>Biological and medical sciences</subject><subject>CABALLOS</subject><subject>CHEVAL</subject><subject>EHRLICHIA</subject><subject>Ehrlichia - genetics</subject><subject>Ehrlichia - immunology</subject><subject>Ehrlichia - ultrastructure</subject><subject>Ehrlichia risticii</subject><subject>Ehrlichiosis - microbiology</subject><subject>Ehrlichiosis - veterinary</subject><subject>Epidemiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GENE</subject><subject>GENES</subject><subject>Horse Diseases - microbiology</subject><subject>Horses</subject><subject>IMMUNOFLUORESCENCE</subject><subject>IMMUNOLOGIE</subject><subject>INMUNOFLUORESCENCIA</subject><subject>INMUNOLOGIA</subject><subject>KENTUCKY</subject><subject>MARYLAND</subject><subject>Mice</subject><subject>Microbiology</subject><subject>OHIO</subject><subject>Polymerase Chain Reaction</subject><subject>PROTEINAS UNICELULARES</subject><subject>PROTEINE MICROBIOLOGIQUE</subject><subject>Rabbits</subject><subject>RIBOSOMAS</subject><subject>RIBOSOME</subject><subject>RNA, Bacterial - genetics</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Sequence Analysis, RNA</subject><subject>TECHNIQUE ANALYTIQUE</subject><subject>TECNICAS ANALITICAS</subject><issn>0095-1137</issn><issn>1098-660X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU-L1DAYh4Mo67j6BQShiHiyNW_SJO3BwzKs_1jxoAt6Cu-kyTRL2oxJx0U_va0zDOrFU0h-zy95w0NIAbQCYM3L9-sPFWcVsIpTJktOOa-gbes7ZAW0bUop6Ze7ZEVpK0oAru6TBznfUAp1LcQZOVOCc9XQFfl6MU5-a0dvXhRDTLs-hrhdNjh280GwZh8wFabHhGayyf_EycexiK4Y7W1x2afgTe-xSD5P3nhf-BwDTjY_JPcchmwfHddzcv368vP6bXn18c279cVVaYQSUymkYNIpZQU2tJa0Y4o51RjWAbQbdIg1NfM_3EbJFhU4Zo0QjVCybjoFlJ-TV4d7d_vNYDtjxylh0LvkB0w_dESv_05G3-tt_K6ZrBm0c__5sZ_it73Nkx58NjYEHG3cZ62Ukhwo_S8IUoqGMZjB5gCaFHNO1p2GAaoXffrGDJozDUwv-vSiTy_65uqTPz9zKh59zfmzY47ZYHAJR-PzCeO8bujvUZ8esN5v-1ufrMY8_PPqDD0-QA6jxu0sUF9_aoVgMIe_ALShuE0</recordid><startdate>19941201</startdate><enddate>19941201</enddate><creator>Chaichanasiriwithaya, W. 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(Ohio State University, Columbus, OH.) ; Rikihisa, Y ; Yamamoto, S ; Reed, S ; Crawford, T.B ; Perryman, L.E ; Palmer, G.H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c575t-56526f77e5a80460d272f78c2d119bafaa40c009fb769a71f2ec55857648d7103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>ADN</topic><topic>Animals</topic><topic>ANTIGENE</topic><topic>ANTIGENOS</topic><topic>ARN RIBOSOMAL</topic><topic>ARN RIBOSOMIAL</topic><topic>BACTERIA</topic><topic>Bacteriology</topic><topic>BACTERIOSE</topic><topic>BACTERIOSIS</topic><topic>Biological and medical sciences</topic><topic>CABALLOS</topic><topic>CHEVAL</topic><topic>EHRLICHIA</topic><topic>Ehrlichia - genetics</topic><topic>Ehrlichia - immunology</topic><topic>Ehrlichia - ultrastructure</topic><topic>Ehrlichia risticii</topic><topic>Ehrlichiosis - microbiology</topic><topic>Ehrlichiosis - veterinary</topic><topic>Epidemiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GENE</topic><topic>GENES</topic><topic>Horse Diseases - microbiology</topic><topic>Horses</topic><topic>IMMUNOFLUORESCENCE</topic><topic>IMMUNOLOGIE</topic><topic>INMUNOFLUORESCENCIA</topic><topic>INMUNOLOGIA</topic><topic>KENTUCKY</topic><topic>MARYLAND</topic><topic>Mice</topic><topic>Microbiology</topic><topic>OHIO</topic><topic>Polymerase Chain Reaction</topic><topic>PROTEINAS UNICELULARES</topic><topic>PROTEINE MICROBIOLOGIQUE</topic><topic>Rabbits</topic><topic>RIBOSOMAS</topic><topic>RIBOSOME</topic><topic>RNA, Bacterial - genetics</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Sequence Analysis, RNA</topic><topic>TECHNIQUE ANALYTIQUE</topic><topic>TECNICAS ANALITICAS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chaichanasiriwithaya, W. (Ohio State University, Columbus, OH.)</creatorcontrib><creatorcontrib>Rikihisa, Y</creatorcontrib><creatorcontrib>Yamamoto, S</creatorcontrib><creatorcontrib>Reed, S</creatorcontrib><creatorcontrib>Crawford, T.B</creatorcontrib><creatorcontrib>Perryman, L.E</creatorcontrib><creatorcontrib>Palmer, G.H</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</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>Chaichanasiriwithaya, W. (Ohio State University, Columbus, OH.)</au><au>Rikihisa, Y</au><au>Yamamoto, S</au><au>Reed, S</au><au>Crawford, T.B</au><au>Perryman, L.E</au><au>Palmer, G.H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antigenic, morphologic, and molecular characterization of new Ehrlichia risticii isolates</atitle><jtitle>Journal of Clinical Microbiology</jtitle><addtitle>J Clin Microbiol</addtitle><date>1994-12-01</date><risdate>1994</risdate><volume>32</volume><issue>12</issue><spage>3026</spage><epage>3033</epage><pages>3026-3033</pages><issn>0095-1137</issn><eissn>1098-660X</eissn><coden>JCMIDW</coden><abstract>Ehrlichia risticii causes an acute infectious disease in horses called Potomac horse fever. To investigate the biological diversity of E. risticii organisms, nine E. risticii isolates derived from the peripheral blood monocytes of clinically sick horses in Ohio and Kentucky during the summers of 1991 and 1993 were compared with Illinois and Virginia isolates originally obtained from horses in Maryland in 1984. Seven of the nine isolates (081, 606, 380, 679, As, Co, and Ov) formed large morulae (tightly packed inclusions of ehrlichial organisms). The remaining isolates, including 1984 isolates, were individually dispersed or formed small morulae in the cytoplasm of P388D1 cells. In Western blot (immunoblot) analysis with four equine and one rabbit polyclonal anti-E. risticii sera, these recent E. risticii isolates showed patterns of antigenic proteins distinct from those of the 1984 isolates and could be divided into three groups: (i) 081; (ii) 606, 022, 067, 380, and 679; and (iii) As, Co, and Ov. By indirect fluorescent antibody labeling with two panels of murine anti-E. risticii (Illinois and Maryland isolates) monoclonal antibodies, isolate 081 was not labeled with any of 20 monoclonal antibodies tested. The remaining isolates were not labeled with several monoclonal antibodies. The digestion pattern with one of the restriction enzymes, AvaII, of the PCR-amplified partial 16S rRNA gene of E. risticii from all Kentucky isolates (As, Co, and Ov) was different from that of Illinois, Virginia, and six Ohio isolates. These results indicate the presence of distinct variants of E. risticii which vary significantly in morpbology, antigenic composition, and the base sequence of the 16S rRNA gene</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>7533780</pmid><doi>10.1128/JCM.32.12.3026-3033.1994</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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source | American Society for Microbiology; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | ADN Animals ANTIGENE ANTIGENOS ARN RIBOSOMAL ARN RIBOSOMIAL BACTERIA Bacteriology BACTERIOSE BACTERIOSIS Biological and medical sciences CABALLOS CHEVAL EHRLICHIA Ehrlichia - genetics Ehrlichia - immunology Ehrlichia - ultrastructure Ehrlichia risticii Ehrlichiosis - microbiology Ehrlichiosis - veterinary Epidemiology Fundamental and applied biological sciences. Psychology GENE GENES Horse Diseases - microbiology Horses IMMUNOFLUORESCENCE IMMUNOLOGIE INMUNOFLUORESCENCIA INMUNOLOGIA KENTUCKY MARYLAND Mice Microbiology OHIO Polymerase Chain Reaction PROTEINAS UNICELULARES PROTEINE MICROBIOLOGIQUE Rabbits RIBOSOMAS RIBOSOME RNA, Bacterial - genetics RNA, Ribosomal, 16S - genetics Sequence Analysis, RNA TECHNIQUE ANALYTIQUE TECNICAS ANALITICAS |
title | Antigenic, morphologic, and molecular characterization of new Ehrlichia risticii isolates |
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