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
Hauptverfasser: Chaichanasiriwithaya, W. (Ohio State University, Columbus, OH.), Rikihisa, Y, Yamamoto, S, Reed, S, Crawford, T.B, Perryman, L.E, Palmer, G.H
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container_title Journal of Clinical Microbiology
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creator Chaichanasiriwithaya, W. (Ohio State University, Columbus, OH.)
Rikihisa, Y
Yamamoto, S
Reed, S
Crawford, T.B
Perryman, L.E
Palmer, G.H
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
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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&amp;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. 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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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ispartof Journal of Clinical Microbiology, 1994-12, Vol.32 (12), p.3026-3033
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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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