Real-Time PCR Investigation of Potential Vectors, Reservoirs, and Shedding Patterns of Feline Hemotropic Mycoplasmas
Three hemotropic mycoplasmas have been identified in pet cats: Mycoplasma haemofelis, "Candidatus Mycoplasma haemominutum," and "Candidatus Mycoplasma turicensis." The way in which these agents are transmitted is largely unknown. Thus, this study aimed to investigate fleas, ticks...
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Veröffentlicht in: | Applied and Environmental Microbiology 2007-06, Vol.73 (12), p.3798-3802 |
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creator | Willi, Barbara Boretti, Felicitas S Meli, Marina L Bernasconi, Marco V Casati, Simona Hegglin, Daniel Puorger, Maria Neimark, Harold Cattori, Valentino Wengi, Nicole Reusch, Claudia E Lutz, Hans Hofmann-Lehmann, Regina |
description | Three hemotropic mycoplasmas have been identified in pet cats: Mycoplasma haemofelis, "Candidatus Mycoplasma haemominutum," and "Candidatus Mycoplasma turicensis." The way in which these agents are transmitted is largely unknown. Thus, this study aimed to investigate fleas, ticks, and rodents as well as saliva and feces from infected cats for the presence of hemotropic mycoplasmas, to gain insight into potential transmission routes for these agents. DNA was extracted from arthropods and from rodent blood or tissue samples from Switzerland and from salivary and fecal swabs from two experimentally infected and six naturally infected cats. All samples were analyzed with real-time PCR, and some positive samples were confirmed by sequencing. Feline hemotropic mycoplasmas were detected in cat fleas and in a few Ixodes sp. and Rhipicephalus sp. ticks collected from animals but not in ticks collected from vegetation or from rodent samples, although the latter were frequently Mycoplasma coccoides PCR positive. When shedding patterns of feline hemotropic mycoplasmas were investigated, "Ca. Mycoplasma turicensis" DNA was detected in saliva and feces at the early but not at the late phase of infection. M. haemofelis and "Ca. Mycoplasma haemominutum" DNA was not amplified from saliva and feces of naturally infected cats, despite high hemotropic mycoplasma blood loads. Our results suggest that besides an ostensibly indirect transmission by fleas, direct transmission through saliva and feces at the early phase of infection could play a role in the epizootiology of feline hemotropic mycoplasmas. Neither the investigated tick nor the rodent population seems to represent a major reservoir for feline hemotropic mycoplasmas in Switzerland. |
doi_str_mv | 10.1128/AEM.02977-06 |
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The way in which these agents are transmitted is largely unknown. Thus, this study aimed to investigate fleas, ticks, and rodents as well as saliva and feces from infected cats for the presence of hemotropic mycoplasmas, to gain insight into potential transmission routes for these agents. DNA was extracted from arthropods and from rodent blood or tissue samples from Switzerland and from salivary and fecal swabs from two experimentally infected and six naturally infected cats. All samples were analyzed with real-time PCR, and some positive samples were confirmed by sequencing. Feline hemotropic mycoplasmas were detected in cat fleas and in a few Ixodes sp. and Rhipicephalus sp. ticks collected from animals but not in ticks collected from vegetation or from rodent samples, although the latter were frequently Mycoplasma coccoides PCR positive. When shedding patterns of feline hemotropic mycoplasmas were investigated, "Ca. Mycoplasma turicensis" DNA was detected in saliva and feces at the early but not at the late phase of infection. M. haemofelis and "Ca. Mycoplasma haemominutum" DNA was not amplified from saliva and feces of naturally infected cats, despite high hemotropic mycoplasma blood loads. Our results suggest that besides an ostensibly indirect transmission by fleas, direct transmission through saliva and feces at the early phase of infection could play a role in the epizootiology of feline hemotropic mycoplasmas. Neither the investigated tick nor the rodent population seems to represent a major reservoir for feline hemotropic mycoplasmas in Switzerland.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/AEM.02977-06</identifier><identifier>PMID: 17468284</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Arthropods - microbiology ; Base Sequence ; Biological and medical sciences ; Body fluids ; Cats ; Cats - microbiology ; Cats - parasitology ; Disease Reservoirs - microbiology ; Disease Vectors ; DNA Primers - genetics ; Feces ; Feces - microbiology ; Fundamental and applied biological sciences. Psychology ; Insects ; Microbiology ; Molecular Sequence Data ; Mycoplasma ; Parasites ; Parasitology ; Polymerase Chain Reaction - methods ; Public Health Microbiology ; Rodentia - microbiology ; Rodents ; Saliva - microbiology ; Sequence Analysis, DNA ; Switzerland</subject><ispartof>Applied and Environmental Microbiology, 2007-06, Vol.73 (12), p.3798-3802</ispartof><rights>2007 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Jun 2007</rights><rights>Copyright © 2007, American Society for Microbiology 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c556t-17da3cae56da91eff106b3685bcdc16ddc07ca2c5d4bc7d69d64731895be13b43</citedby><cites>FETCH-LOGICAL-c556t-17da3cae56da91eff106b3685bcdc16ddc07ca2c5d4bc7d69d64731895be13b43</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/PMC1932730/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1932730/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,3176,3177,27906,27907,53773,53775</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18859632$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17468284$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Willi, Barbara</creatorcontrib><creatorcontrib>Boretti, Felicitas S</creatorcontrib><creatorcontrib>Meli, Marina L</creatorcontrib><creatorcontrib>Bernasconi, Marco V</creatorcontrib><creatorcontrib>Casati, Simona</creatorcontrib><creatorcontrib>Hegglin, Daniel</creatorcontrib><creatorcontrib>Puorger, Maria</creatorcontrib><creatorcontrib>Neimark, Harold</creatorcontrib><creatorcontrib>Cattori, Valentino</creatorcontrib><creatorcontrib>Wengi, Nicole</creatorcontrib><creatorcontrib>Reusch, Claudia E</creatorcontrib><creatorcontrib>Lutz, Hans</creatorcontrib><creatorcontrib>Hofmann-Lehmann, Regina</creatorcontrib><title>Real-Time PCR Investigation of Potential Vectors, Reservoirs, and Shedding Patterns of Feline Hemotropic Mycoplasmas</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Three hemotropic mycoplasmas have been identified in pet cats: Mycoplasma haemofelis, "Candidatus Mycoplasma haemominutum," and "Candidatus Mycoplasma turicensis." The way in which these agents are transmitted is largely unknown. Thus, this study aimed to investigate fleas, ticks, and rodents as well as saliva and feces from infected cats for the presence of hemotropic mycoplasmas, to gain insight into potential transmission routes for these agents. DNA was extracted from arthropods and from rodent blood or tissue samples from Switzerland and from salivary and fecal swabs from two experimentally infected and six naturally infected cats. All samples were analyzed with real-time PCR, and some positive samples were confirmed by sequencing. Feline hemotropic mycoplasmas were detected in cat fleas and in a few Ixodes sp. and Rhipicephalus sp. ticks collected from animals but not in ticks collected from vegetation or from rodent samples, although the latter were frequently Mycoplasma coccoides PCR positive. When shedding patterns of feline hemotropic mycoplasmas were investigated, "Ca. Mycoplasma turicensis" DNA was detected in saliva and feces at the early but not at the late phase of infection. M. haemofelis and "Ca. Mycoplasma haemominutum" DNA was not amplified from saliva and feces of naturally infected cats, despite high hemotropic mycoplasma blood loads. Our results suggest that besides an ostensibly indirect transmission by fleas, direct transmission through saliva and feces at the early phase of infection could play a role in the epizootiology of feline hemotropic mycoplasmas. Neither the investigated tick nor the rodent population seems to represent a major reservoir for feline hemotropic mycoplasmas in Switzerland.</description><subject>Animals</subject><subject>Arthropods - microbiology</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Body fluids</subject><subject>Cats</subject><subject>Cats - microbiology</subject><subject>Cats - parasitology</subject><subject>Disease Reservoirs - microbiology</subject><subject>Disease Vectors</subject><subject>DNA Primers - genetics</subject><subject>Feces</subject><subject>Feces - microbiology</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Insects</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Mycoplasma</topic><topic>Parasites</topic><topic>Parasitology</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Public Health Microbiology</topic><topic>Rodentia - microbiology</topic><topic>Rodents</topic><topic>Saliva - microbiology</topic><topic>Sequence Analysis, DNA</topic><topic>Switzerland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Willi, Barbara</creatorcontrib><creatorcontrib>Boretti, Felicitas S</creatorcontrib><creatorcontrib>Meli, Marina L</creatorcontrib><creatorcontrib>Bernasconi, Marco V</creatorcontrib><creatorcontrib>Casati, Simona</creatorcontrib><creatorcontrib>Hegglin, Daniel</creatorcontrib><creatorcontrib>Puorger, Maria</creatorcontrib><creatorcontrib>Neimark, Harold</creatorcontrib><creatorcontrib>Cattori, Valentino</creatorcontrib><creatorcontrib>Wengi, Nicole</creatorcontrib><creatorcontrib>Reusch, Claudia E</creatorcontrib><creatorcontrib>Lutz, Hans</creatorcontrib><creatorcontrib>Hofmann-Lehmann, Regina</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>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Willi, Barbara</au><au>Boretti, Felicitas S</au><au>Meli, Marina L</au><au>Bernasconi, Marco V</au><au>Casati, Simona</au><au>Hegglin, Daniel</au><au>Puorger, Maria</au><au>Neimark, Harold</au><au>Cattori, Valentino</au><au>Wengi, Nicole</au><au>Reusch, Claudia E</au><au>Lutz, Hans</au><au>Hofmann-Lehmann, Regina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-Time PCR Investigation of Potential Vectors, Reservoirs, and Shedding Patterns of Feline Hemotropic Mycoplasmas</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2007-06-01</date><risdate>2007</risdate><volume>73</volume><issue>12</issue><spage>3798</spage><epage>3802</epage><pages>3798-3802</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>Three hemotropic mycoplasmas have been identified in pet cats: Mycoplasma haemofelis, "Candidatus Mycoplasma haemominutum," and "Candidatus Mycoplasma turicensis." The way in which these agents are transmitted is largely unknown. Thus, this study aimed to investigate fleas, ticks, and rodents as well as saliva and feces from infected cats for the presence of hemotropic mycoplasmas, to gain insight into potential transmission routes for these agents. DNA was extracted from arthropods and from rodent blood or tissue samples from Switzerland and from salivary and fecal swabs from two experimentally infected and six naturally infected cats. All samples were analyzed with real-time PCR, and some positive samples were confirmed by sequencing. Feline hemotropic mycoplasmas were detected in cat fleas and in a few Ixodes sp. and Rhipicephalus sp. ticks collected from animals but not in ticks collected from vegetation or from rodent samples, although the latter were frequently Mycoplasma coccoides PCR positive. When shedding patterns of feline hemotropic mycoplasmas were investigated, "Ca. Mycoplasma turicensis" DNA was detected in saliva and feces at the early but not at the late phase of infection. M. haemofelis and "Ca. Mycoplasma haemominutum" DNA was not amplified from saliva and feces of naturally infected cats, despite high hemotropic mycoplasma blood loads. Our results suggest that besides an ostensibly indirect transmission by fleas, direct transmission through saliva and feces at the early phase of infection could play a role in the epizootiology of feline hemotropic mycoplasmas. Neither the investigated tick nor the rodent population seems to represent a major reservoir for feline hemotropic mycoplasmas in Switzerland.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>17468284</pmid><doi>10.1128/AEM.02977-06</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Arthropods - microbiology Base Sequence Biological and medical sciences Body fluids Cats Cats - microbiology Cats - parasitology Disease Reservoirs - microbiology Disease Vectors DNA Primers - genetics Feces Feces - microbiology Fundamental and applied biological sciences. Psychology Insects Microbiology Molecular Sequence Data Mycoplasma Parasites Parasitology Polymerase Chain Reaction - methods Public Health Microbiology Rodentia - microbiology Rodents Saliva - microbiology Sequence Analysis, DNA Switzerland |
title | Real-Time PCR Investigation of Potential Vectors, Reservoirs, and Shedding Patterns of Feline Hemotropic Mycoplasmas |
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