Decontamination of mycoplasma-contaminated Orientia tsutsugamushi strains by repeating passages through cell cultures with antibiotics
Mycoplasmas-contamination of Orientia tsutsugamushi, one of the obligated intracellular bacteria, is a very serious problem in in vitro studies using cell cultures because mycoplasmas have significant influence on the results of scientific studies. Only a recommended decontamination method is to pas...
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description | Mycoplasmas-contamination of Orientia tsutsugamushi, one of the obligated intracellular bacteria, is a very serious problem in in vitro studies using cell cultures because mycoplasmas have significant influence on the results of scientific studies. Only a recommended decontamination method is to passage the contaminated O. tsutsugamushi strains through mice to eliminate only mycoplasmas under influence of their immunity. However, this method sometimes does not work especially for low virulent strains of O. tsutsugamushi which are difficult to propagate in mice. In this study, we tried to eliminate mycoplasmas contaminants from both high virulent and low virulent strains of the contaminated O. tsutsugamushi by repeating passage through cell cultures with antibiotics in vitro.
We cultured a contaminated, high virulent strain of O. tsutsugamushi using a mouse lung fibroblasts cell line, L-929 cell in the culture medium containing lincomycin at various concentrations and repeated passages about every seven days. At the passage 5 only with 10 μg/ml of lincomycin, we did not detect mycoplasmas by two PCR based methods whereas O. tsutsugamushi continued good growth. During following four passages without lincomycin, mycoplasmas did not recover. These results suggested that mycoplasmas were completely eliminated from the high virulent strain of O. tsutsugamushi. Furthermore, by the same procedures with 10 μg/ml of lincomycin, we also eliminated mycoplasmas from a contaminated, low virulent strain of O. tsutsugamushi. Our additional assay showed that 50 μg/ml of lyncomycin did not inhibit the growth of O. tsutsugamushi, although MICs of many mycoplasmas contaminants were less than 6 μg/ml as shown previously.
Our results showed an alternative method to eliminate mycoplasmas from the contaminated O. tsutsugamushi strains in place of in vivo passage through mice. Especially this notable method works for the decontamination not only from the high virulent strain also from the low virulent strain of O. tsutsugamushi. For further elimination, lincomycin at the limit concentration, which does not inhibit the growth of O. tsutsugamushi, can possibly eliminate most mycoplasmas from contaminated O. tsutsugamushi strains. |
doi_str_mv | 10.1186/1471-2180-13-32 |
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We cultured a contaminated, high virulent strain of O. tsutsugamushi using a mouse lung fibroblasts cell line, L-929 cell in the culture medium containing lincomycin at various concentrations and repeated passages about every seven days. At the passage 5 only with 10 μg/ml of lincomycin, we did not detect mycoplasmas by two PCR based methods whereas O. tsutsugamushi continued good growth. During following four passages without lincomycin, mycoplasmas did not recover. These results suggested that mycoplasmas were completely eliminated from the high virulent strain of O. tsutsugamushi. Furthermore, by the same procedures with 10 μg/ml of lincomycin, we also eliminated mycoplasmas from a contaminated, low virulent strain of O. tsutsugamushi. Our additional assay showed that 50 μg/ml of lyncomycin did not inhibit the growth of O. tsutsugamushi, although MICs of many mycoplasmas contaminants were less than 6 μg/ml as shown previously.
Our results showed an alternative method to eliminate mycoplasmas from the contaminated O. tsutsugamushi strains in place of in vivo passage through mice. Especially this notable method works for the decontamination not only from the high virulent strain also from the low virulent strain of O. tsutsugamushi. For further elimination, lincomycin at the limit concentration, which does not inhibit the growth of O. tsutsugamushi, can possibly eliminate most mycoplasmas from contaminated O. tsutsugamushi strains.</description><identifier>ISSN: 1471-2180</identifier><identifier>EISSN: 1471-2180</identifier><identifier>DOI: 10.1186/1471-2180-13-32</identifier><identifier>PMID: 23394970</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Animals ; Anti-Bacterial Agents - pharmacology ; Antibiotics ; Bacteria ; Cell culture ; Cell Culture Techniques - methods ; Cell Line ; Contaminants ; Culture Media - chemistry ; Decontamination ; Decontamination - methods ; Fibroblasts ; Fibroblasts - microbiology ; Gram-negative bacteria ; Immunity ; Lincomycin ; Lincomycin - pharmacology ; Lung ; Methodology ; Methods ; Mice ; Microbiology ; Minimum inhibitory concentration ; Mycoplasma ; Mycoplasma - drug effects ; Orientia tsutsugamushi ; Orientia tsutsugamushi - growth & development ; Orientia tsutsugamushi - isolation & purification ; Polymerase chain reaction ; Serial Passage ; Typhus</subject><ispartof>BMC microbiology, 2013-02, Vol.13 (1), p.32-32</ispartof><rights>2013 Ogawa et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright ©2013 Ogawa et al.; licensee BioMed Central Ltd. 2013 Ogawa et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b513t-367b635e1b3987a202c8520a5ce8c3d1e90fc88b052e932d59421f1361c4c4103</citedby><cites>FETCH-LOGICAL-b513t-367b635e1b3987a202c8520a5ce8c3d1e90fc88b052e932d59421f1361c4c4103</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/PMC3598641/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598641/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23394970$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ogawa, Motohiko</creatorcontrib><creatorcontrib>Uchiyama, Tsuneo</creatorcontrib><creatorcontrib>Satoh, Masaaki</creatorcontrib><creatorcontrib>Ando, Shuji</creatorcontrib><title>Decontamination of mycoplasma-contaminated Orientia tsutsugamushi strains by repeating passages through cell cultures with antibiotics</title><title>BMC microbiology</title><addtitle>BMC Microbiol</addtitle><description>Mycoplasmas-contamination of Orientia tsutsugamushi, one of the obligated intracellular bacteria, is a very serious problem in in vitro studies using cell cultures because mycoplasmas have significant influence on the results of scientific studies. Only a recommended decontamination method is to passage the contaminated O. tsutsugamushi strains through mice to eliminate only mycoplasmas under influence of their immunity. However, this method sometimes does not work especially for low virulent strains of O. tsutsugamushi which are difficult to propagate in mice. In this study, we tried to eliminate mycoplasmas contaminants from both high virulent and low virulent strains of the contaminated O. tsutsugamushi by repeating passage through cell cultures with antibiotics in vitro.
We cultured a contaminated, high virulent strain of O. tsutsugamushi using a mouse lung fibroblasts cell line, L-929 cell in the culture medium containing lincomycin at various concentrations and repeated passages about every seven days. At the passage 5 only with 10 μg/ml of lincomycin, we did not detect mycoplasmas by two PCR based methods whereas O. tsutsugamushi continued good growth. During following four passages without lincomycin, mycoplasmas did not recover. These results suggested that mycoplasmas were completely eliminated from the high virulent strain of O. tsutsugamushi. Furthermore, by the same procedures with 10 μg/ml of lincomycin, we also eliminated mycoplasmas from a contaminated, low virulent strain of O. tsutsugamushi. Our additional assay showed that 50 μg/ml of lyncomycin did not inhibit the growth of O. tsutsugamushi, although MICs of many mycoplasmas contaminants were less than 6 μg/ml as shown previously.
Our results showed an alternative method to eliminate mycoplasmas from the contaminated O. tsutsugamushi strains in place of in vivo passage through mice. Especially this notable method works for the decontamination not only from the high virulent strain also from the low virulent strain of O. tsutsugamushi. For further elimination, lincomycin at the limit concentration, which does not inhibit the growth of O. tsutsugamushi, can possibly eliminate most mycoplasmas from contaminated O. tsutsugamushi strains.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antibiotics</subject><subject>Bacteria</subject><subject>Cell culture</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Line</subject><subject>Contaminants</subject><subject>Culture Media - chemistry</subject><subject>Decontamination</subject><subject>Decontamination - methods</subject><subject>Fibroblasts</subject><subject>Fibroblasts - microbiology</subject><subject>Gram-negative bacteria</subject><subject>Immunity</subject><subject>Lincomycin</subject><subject>Lincomycin - pharmacology</subject><subject>Lung</subject><subject>Methodology</subject><subject>Methods</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Minimum inhibitory concentration</subject><subject>Mycoplasma</subject><subject>Mycoplasma - drug effects</subject><subject>Orientia tsutsugamushi</subject><subject>Orientia tsutsugamushi - growth & development</subject><subject>Orientia tsutsugamushi - isolation & purification</subject><subject>Polymerase chain reaction</subject><subject>Serial Passage</subject><subject>Typhus</subject><issn>1471-2180</issn><issn>1471-2180</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkk1rFTEUhoNYbK2u3UnATTdjc5LMTGYjaP0qFLrRdcjkZmZSZpIxH5b7B_zd5nLrtRUFIZBwzsPLm_cchF4AeQ0gmnPgLVQUBKmAVYw-QieHyuN772P0NMYbQqAVrH2CjiljHe9acoJ-vDfau6QW61Sy3mE_4GWr_TqruKjqd89s8HWwxiWrcIq5nFEtOU4WxxSUdRH3WxzMaoqMG_GqYlSjiThNwedxwtrMM9Z5TjmU6q1NE1ZFrLc-WR2foaNBzdE8v7tP0dePH75cfK6urj9dXry9qvoaWKpY0_YNqw30rBOtooRqUVOiam2EZhswHRm0ED2pqekY3dQdpzAAa0BzzYGwU_Rmr7vmfjEbXf4T1CzXYBcVttIrKx92nJ3k6L9LVnei4VAE3u0FivF_CDzsaL_I3Rzkbg4SmGS0iJzduQj-WzYxycXGXUDKGZ9joSgThHDxP2iZKRccuoK--gO98Tm4EueO4gJaoKJQ53tKBx9jMMPBOxR7Zaf-4vbl_cwO_K8lYj8BXurKnA</recordid><startdate>20130208</startdate><enddate>20130208</enddate><creator>Ogawa, Motohiko</creator><creator>Uchiyama, Tsuneo</creator><creator>Satoh, Masaaki</creator><creator>Ando, Shuji</creator><general>BioMed Central</general><general>BioMed Central Ltd</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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130208</creationdate><title>Decontamination of mycoplasma-contaminated Orientia tsutsugamushi strains by repeating passages through cell cultures with antibiotics</title><author>Ogawa, Motohiko ; Uchiyama, Tsuneo ; Satoh, Masaaki ; Ando, Shuji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b513t-367b635e1b3987a202c8520a5ce8c3d1e90fc88b052e932d59421f1361c4c4103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogawa, Motohiko</au><au>Uchiyama, Tsuneo</au><au>Satoh, Masaaki</au><au>Ando, Shuji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decontamination of mycoplasma-contaminated Orientia tsutsugamushi strains by repeating passages through cell cultures with antibiotics</atitle><jtitle>BMC microbiology</jtitle><addtitle>BMC Microbiol</addtitle><date>2013-02-08</date><risdate>2013</risdate><volume>13</volume><issue>1</issue><spage>32</spage><epage>32</epage><pages>32-32</pages><issn>1471-2180</issn><eissn>1471-2180</eissn><abstract>Mycoplasmas-contamination of Orientia tsutsugamushi, one of the obligated intracellular bacteria, is a very serious problem in in vitro studies using cell cultures because mycoplasmas have significant influence on the results of scientific studies. Only a recommended decontamination method is to passage the contaminated O. tsutsugamushi strains through mice to eliminate only mycoplasmas under influence of their immunity. However, this method sometimes does not work especially for low virulent strains of O. tsutsugamushi which are difficult to propagate in mice. In this study, we tried to eliminate mycoplasmas contaminants from both high virulent and low virulent strains of the contaminated O. tsutsugamushi by repeating passage through cell cultures with antibiotics in vitro.
We cultured a contaminated, high virulent strain of O. tsutsugamushi using a mouse lung fibroblasts cell line, L-929 cell in the culture medium containing lincomycin at various concentrations and repeated passages about every seven days. At the passage 5 only with 10 μg/ml of lincomycin, we did not detect mycoplasmas by two PCR based methods whereas O. tsutsugamushi continued good growth. During following four passages without lincomycin, mycoplasmas did not recover. These results suggested that mycoplasmas were completely eliminated from the high virulent strain of O. tsutsugamushi. Furthermore, by the same procedures with 10 μg/ml of lincomycin, we also eliminated mycoplasmas from a contaminated, low virulent strain of O. tsutsugamushi. Our additional assay showed that 50 μg/ml of lyncomycin did not inhibit the growth of O. tsutsugamushi, although MICs of many mycoplasmas contaminants were less than 6 μg/ml as shown previously.
Our results showed an alternative method to eliminate mycoplasmas from the contaminated O. tsutsugamushi strains in place of in vivo passage through mice. Especially this notable method works for the decontamination not only from the high virulent strain also from the low virulent strain of O. tsutsugamushi. For further elimination, lincomycin at the limit concentration, which does not inhibit the growth of O. tsutsugamushi, can possibly eliminate most mycoplasmas from contaminated O. tsutsugamushi strains.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>23394970</pmid><doi>10.1186/1471-2180-13-32</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anti-Bacterial Agents - pharmacology Antibiotics Bacteria Cell culture Cell Culture Techniques - methods Cell Line Contaminants Culture Media - chemistry Decontamination Decontamination - methods Fibroblasts Fibroblasts - microbiology Gram-negative bacteria Immunity Lincomycin Lincomycin - pharmacology Lung Methodology Methods Mice Microbiology Minimum inhibitory concentration Mycoplasma Mycoplasma - drug effects Orientia tsutsugamushi Orientia tsutsugamushi - growth & development Orientia tsutsugamushi - isolation & purification Polymerase chain reaction Serial Passage Typhus |
title | Decontamination of mycoplasma-contaminated Orientia tsutsugamushi strains by repeating passages through cell cultures with antibiotics |
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