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The first isolation, in vitro propagation, and genetic characterization of Ehrlichia canis in Israel
Ehrlichia canis, the etiologic agent of canine ehrlichiosis, was isolated in Israel from a naturally infected dog with acute signs of the disease. The organism designated E. canis 611, was passaged experimentally to a beagle, from which it was propagated in primary canine monocytes. The organism was...
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Published in: | Veterinary parasitology 1996-04, Vol.62 (3), p.331-340 |
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container_title | Veterinary parasitology |
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creator | Keysary, Avi Waner, Trevor Rosner, Miri Warner, Cynthia K. Dawson, Jacqueline E. Zass, Rosa Biggie, Kristine L. Harrus, Shimon |
description | Ehrlichia canis, the etiologic agent of canine ehrlichiosis, was isolated in Israel from a naturally infected dog with acute signs of the disease. The organism designated
E. canis 611, was passaged experimentally to a beagle, from which it was propagated in primary canine monocytes. The organism was then grown in vitro in a continuous canine cell line, DH82. Nine beagles subsequently injected with whole
E. canis-infected blood all developed typical symptoms of ehrlichiosis. An indirect immunofluorescence antibody test to
E. canis was developed and compared with a commercial kit, revealing a good correlation between the two assays. Transmission electron microscopy of DH82 cells infected with the Israeli strain of
E. canis (611), revealed organisms similar to those described in the literature: two different forms of morulae appeared, one tightly, the other loosely, packed. The 16S rRNA gene sequence obtained from the Israeli
Ehrlichia isolate was compared with other isolates,
E. canis Oklahoma and
E. canis Florida. The Israeli strain 16S rRNA had three nucleotide differences from the Oklahoma isolate, and four nucleotide differences from the Florida isolate, in addition to one nucleotide gap in each. The Israeli isolate was found to be 0.54% different from the Oklahoma strain, and 0.61% different from the Florida strain. These are the same magnitudes of differences displayed by the other most closely related group in the phylogenetic tree, namely
Ehrlichia equi, Ehrlichia phagocytophilia and the human granulocytic ehrlichia. |
doi_str_mv | 10.1016/0304-4017(95)00866-7 |
format | article |
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E. canis 611, was passaged experimentally to a beagle, from which it was propagated in primary canine monocytes. The organism was then grown in vitro in a continuous canine cell line, DH82. Nine beagles subsequently injected with whole
E. canis-infected blood all developed typical symptoms of ehrlichiosis. An indirect immunofluorescence antibody test to
E. canis was developed and compared with a commercial kit, revealing a good correlation between the two assays. Transmission electron microscopy of DH82 cells infected with the Israeli strain of
E. canis (611), revealed organisms similar to those described in the literature: two different forms of morulae appeared, one tightly, the other loosely, packed. The 16S rRNA gene sequence obtained from the Israeli
Ehrlichia isolate was compared with other isolates,
E. canis Oklahoma and
E. canis Florida. The Israeli strain 16S rRNA had three nucleotide differences from the Oklahoma isolate, and four nucleotide differences from the Florida isolate, in addition to one nucleotide gap in each. The Israeli isolate was found to be 0.54% different from the Oklahoma strain, and 0.61% different from the Florida strain. These are the same magnitudes of differences displayed by the other most closely related group in the phylogenetic tree, namely
Ehrlichia equi, Ehrlichia phagocytophilia and the human granulocytic ehrlichia.</description><identifier>ISSN: 0304-4017</identifier><identifier>EISSN: 1873-2550</identifier><identifier>DOI: 10.1016/0304-4017(95)00866-7</identifier><identifier>PMID: 8686178</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antibodies, Bacterial - blood ; Cell Line ; DNA, Ribosomal - analysis ; Dog Diseases ; Dog-Rickettsia ; Dogs ; Ehrlichia - genetics ; Ehrlichia - growth & development ; Ehrlichia - isolation & purification ; Ehrlichia canis ; Ehrlichiosis - blood ; Ehrlichiosis - diagnosis ; Ehrlichiosis - veterinary ; Florida ; Fluorescent Antibody Technique, Indirect ; Genes, Bacterial ; Humans ; Israel ; Microscopy, Electron ; Molecular Sequence Data ; Monocytes - microbiology ; Oklahoma ; Phylogeny ; Reagent Kits, Diagnostic ; RNA, Ribosomal, 16S - genetics</subject><ispartof>Veterinary parasitology, 1996-04, Vol.62 (3), p.331-340</ispartof><rights>1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c388t-fbe3f3f07424852921f707af5294ecfc2a8830c7d945a07a324e5ed637e9fc8c3</citedby><cites>FETCH-LOGICAL-c388t-fbe3f3f07424852921f707af5294ecfc2a8830c7d945a07a324e5ed637e9fc8c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8686178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Keysary, Avi</creatorcontrib><creatorcontrib>Waner, Trevor</creatorcontrib><creatorcontrib>Rosner, Miri</creatorcontrib><creatorcontrib>Warner, Cynthia K.</creatorcontrib><creatorcontrib>Dawson, Jacqueline E.</creatorcontrib><creatorcontrib>Zass, Rosa</creatorcontrib><creatorcontrib>Biggie, Kristine L.</creatorcontrib><creatorcontrib>Harrus, Shimon</creatorcontrib><title>The first isolation, in vitro propagation, and genetic characterization of Ehrlichia canis in Israel</title><title>Veterinary parasitology</title><addtitle>Vet Parasitol</addtitle><description>Ehrlichia canis, the etiologic agent of canine ehrlichiosis, was isolated in Israel from a naturally infected dog with acute signs of the disease. The organism designated
E. canis 611, was passaged experimentally to a beagle, from which it was propagated in primary canine monocytes. The organism was then grown in vitro in a continuous canine cell line, DH82. Nine beagles subsequently injected with whole
E. canis-infected blood all developed typical symptoms of ehrlichiosis. An indirect immunofluorescence antibody test to
E. canis was developed and compared with a commercial kit, revealing a good correlation between the two assays. Transmission electron microscopy of DH82 cells infected with the Israeli strain of
E. canis (611), revealed organisms similar to those described in the literature: two different forms of morulae appeared, one tightly, the other loosely, packed. The 16S rRNA gene sequence obtained from the Israeli
Ehrlichia isolate was compared with other isolates,
E. canis Oklahoma and
E. canis Florida. The Israeli strain 16S rRNA had three nucleotide differences from the Oklahoma isolate, and four nucleotide differences from the Florida isolate, in addition to one nucleotide gap in each. The Israeli isolate was found to be 0.54% different from the Oklahoma strain, and 0.61% different from the Florida strain. These are the same magnitudes of differences displayed by the other most closely related group in the phylogenetic tree, namely
Ehrlichia equi, Ehrlichia phagocytophilia and the human granulocytic ehrlichia.</description><subject>Animals</subject><subject>Antibodies, Bacterial - blood</subject><subject>Cell Line</subject><subject>DNA, Ribosomal - analysis</subject><subject>Dog Diseases</subject><subject>Dog-Rickettsia</subject><subject>Dogs</subject><subject>Ehrlichia - genetics</subject><subject>Ehrlichia - growth & development</subject><subject>Ehrlichia - isolation & purification</subject><subject>Ehrlichia canis</subject><subject>Ehrlichiosis - blood</subject><subject>Ehrlichiosis - diagnosis</subject><subject>Ehrlichiosis - veterinary</subject><subject>Florida</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Genes, Bacterial</subject><subject>Humans</subject><subject>Israel</subject><subject>Microscopy, Electron</subject><subject>Molecular Sequence Data</subject><subject>Monocytes - microbiology</subject><subject>Oklahoma</subject><subject>Phylogeny</subject><subject>Reagent Kits, Diagnostic</subject><subject>RNA, Ribosomal, 16S - genetics</subject><issn>0304-4017</issn><issn>1873-2550</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqFkUFLAzEQhYMoWqv_QCEnUXB1sskm2YsgpWpB8FLPIc1ObGS7W5NtQX-9W1s86mnCvDdvwjeEnDG4YcDkLXAQmQCmLsviCkBLmak9MmBa8SwvCtgng1_LETlO6R0ABEh1SA611JIpPSDVdI7Uh5g6GlJb2y60zTUNDV2HLrZ0Gdulfdt1bVPRN2ywC466uY3WdRjD149KW0_H81gHNw-WOtuEtEmZpGixPiEH3tYJT3d1SF4fxtPRU_b88jgZ3T9njmvdZX6G3HMPSuRCF3mZM69AWd8_BTrvcqs1B6eqUhS2F3gusMBKcoWld9rxIbnY5vbf_lhh6swiJId1bRtsV8koDTIvBP_XyKToySnRG8XW6GKbUkRvljEsbPw0DMzmCmaD2GwQm7IwP1cwqh873-WvZgusfod22Hv9bqtjT2MdMJrkAjYOqxDRdaZqw98LvgEGUZax</recordid><startdate>19960401</startdate><enddate>19960401</enddate><creator>Keysary, Avi</creator><creator>Waner, Trevor</creator><creator>Rosner, Miri</creator><creator>Warner, Cynthia K.</creator><creator>Dawson, Jacqueline E.</creator><creator>Zass, Rosa</creator><creator>Biggie, Kristine L.</creator><creator>Harrus, Shimon</creator><general>Elsevier B.V</general><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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>19960401</creationdate><title>The first isolation, in vitro propagation, and genetic characterization of Ehrlichia canis in Israel</title><author>Keysary, Avi ; 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The organism designated
E. canis 611, was passaged experimentally to a beagle, from which it was propagated in primary canine monocytes. The organism was then grown in vitro in a continuous canine cell line, DH82. Nine beagles subsequently injected with whole
E. canis-infected blood all developed typical symptoms of ehrlichiosis. An indirect immunofluorescence antibody test to
E. canis was developed and compared with a commercial kit, revealing a good correlation between the two assays. Transmission electron microscopy of DH82 cells infected with the Israeli strain of
E. canis (611), revealed organisms similar to those described in the literature: two different forms of morulae appeared, one tightly, the other loosely, packed. The 16S rRNA gene sequence obtained from the Israeli
Ehrlichia isolate was compared with other isolates,
E. canis Oklahoma and
E. canis Florida. The Israeli strain 16S rRNA had three nucleotide differences from the Oklahoma isolate, and four nucleotide differences from the Florida isolate, in addition to one nucleotide gap in each. The Israeli isolate was found to be 0.54% different from the Oklahoma strain, and 0.61% different from the Florida strain. These are the same magnitudes of differences displayed by the other most closely related group in the phylogenetic tree, namely
Ehrlichia equi, Ehrlichia phagocytophilia and the human granulocytic ehrlichia.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>8686178</pmid><doi>10.1016/0304-4017(95)00866-7</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Antibodies, Bacterial - blood Cell Line DNA, Ribosomal - analysis Dog Diseases Dog-Rickettsia Dogs Ehrlichia - genetics Ehrlichia - growth & development Ehrlichia - isolation & purification Ehrlichia canis Ehrlichiosis - blood Ehrlichiosis - diagnosis Ehrlichiosis - veterinary Florida Fluorescent Antibody Technique, Indirect Genes, Bacterial Humans Israel Microscopy, Electron Molecular Sequence Data Monocytes - microbiology Oklahoma Phylogeny Reagent Kits, Diagnostic RNA, Ribosomal, 16S - genetics |
title | The first isolation, in vitro propagation, and genetic characterization of Ehrlichia canis in Israel |
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