The susceptibility of ionophore-resistant Clostridium aminophilum Fto other antibiotics
Objective: To determine if ionophore-resistant ruminal bacteria are cross-resistant to other classes of antibiotics. Clostridium aminophilum was used as a model organism because this Gram-positive ruminal bacterium can adapt to ionophores (monensin and lasalocid). Non-adapted cultures lagged for at...
Gespeichert in:
Veröffentlicht in: | Journal of antimicrobial chemotherapy 2003-10, Vol.52 (4), p.623-628 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 628 |
---|---|
container_issue | 4 |
container_start_page | 623 |
container_title | Journal of antimicrobial chemotherapy |
container_volume | 52 |
creator | Houlihan, A. J. |
description | Objective: To determine if ionophore-resistant ruminal bacteria are cross-resistant to other classes of antibiotics. Clostridium aminophilum was used as a model organism because this Gram-positive ruminal bacterium can adapt to ionophores (monensin and lasalocid). Non-adapted cultures lagged for at least 12 h with 1 [mu]M monensin or lasalocid, but initiated no growth if the concentration was 10 [mu]M. Adapted cultures did not lag with 1 [mu]M monensin or lasalocid, grew well even if the ionophore concentration was 10 [mu]M and contained cells at least 100 000-fold more resistant than those in non-adapted cultures. Methods: Ionophore-adapted and non-adapted cultures were assayed for their susceptibility to other classes of antibiotics (penicillin G, ampicillin, cephalosporin C, vancomycin, carbenicillin, tetracycline, chloramphenicol, erythromycin, streptomycin, linocomycin, rifampicin, trimethoprim, novobiocin, polymyxin B and bacitracin) using a broth microdilution method. Results: Adapted cultures retained their resistance phenotype for at least 28 generations even if ionophore was no longer present. Monensin-adapted cultures were as resistant to lasalocid as those adapted to lasalocid, but lasalocid-adapted cultures lagged with 1 [mu]M monensin. Monensin- and lasalocid-resistant C. aminophilum F cultures were as susceptible to most antibiotics as non-adapted cultures. The only antibiotic that seemed to have a common mechanism of resistance was bacitracin, and the ionophore-adapted cultures had a 32-fold greater MIC. Conclusion: The use of ionophores in cattle feed and the selection of ionophore-resistant ruminal bacteria does not necessarily lead to other types of antibiotic resistance. |
doi_str_mv | 10.1093/jac/dkg398 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_217663329</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>431326411</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1039-3c678bb02e08de91fb38f1cc0b6b9d6c184674cfb761a4170e3d2391143a3f9c3</originalsourceid><addsrcrecordid>eNpNkLFOwzAURS0EEqWw8AUWI1KoX15w4hFVFJAqsRQxWrZjU5e0DrYz9O9JFQame4eje6VDyC2wB2ACFztlFu33F4rmjMyg4qwomYDzf_2SXKW0Y4zxR97MyOdma2kakrF99tp3Ph9pcNSHQ-i3Idoi2uRTVodMl11IOfrWD3uq9v4E-G7sqxxoyFsb6UiNGyF7k67JhVNdsjd_OScfq-fN8rVYv7-8LZ_WhQGGokDD60ZrVlrWtFaA09g4MIZprkXLDTQVryvjdM1BVVAzi22JAqBChU4YnJO7abeP4WewKctdGOJhvJQl1JwjlmKE7ifIxJBStE720e9VPEpg8uRNjt7k5A1_AbzyYuQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>217663329</pqid></control><display><type>article</type><title>The susceptibility of ionophore-resistant Clostridium aminophilum Fto other antibiotics</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>Free Full-Text Journals in Chemistry</source><creator>Houlihan, A. J.</creator><creatorcontrib>Houlihan, A. J.</creatorcontrib><description>Objective: To determine if ionophore-resistant ruminal bacteria are cross-resistant to other classes of antibiotics. Clostridium aminophilum was used as a model organism because this Gram-positive ruminal bacterium can adapt to ionophores (monensin and lasalocid). Non-adapted cultures lagged for at least 12 h with 1 [mu]M monensin or lasalocid, but initiated no growth if the concentration was 10 [mu]M. Adapted cultures did not lag with 1 [mu]M monensin or lasalocid, grew well even if the ionophore concentration was 10 [mu]M and contained cells at least 100 000-fold more resistant than those in non-adapted cultures. Methods: Ionophore-adapted and non-adapted cultures were assayed for their susceptibility to other classes of antibiotics (penicillin G, ampicillin, cephalosporin C, vancomycin, carbenicillin, tetracycline, chloramphenicol, erythromycin, streptomycin, linocomycin, rifampicin, trimethoprim, novobiocin, polymyxin B and bacitracin) using a broth microdilution method. Results: Adapted cultures retained their resistance phenotype for at least 28 generations even if ionophore was no longer present. Monensin-adapted cultures were as resistant to lasalocid as those adapted to lasalocid, but lasalocid-adapted cultures lagged with 1 [mu]M monensin. Monensin- and lasalocid-resistant C. aminophilum F cultures were as susceptible to most antibiotics as non-adapted cultures. The only antibiotic that seemed to have a common mechanism of resistance was bacitracin, and the ionophore-adapted cultures had a 32-fold greater MIC. Conclusion: The use of ionophores in cattle feed and the selection of ionophore-resistant ruminal bacteria does not necessarily lead to other types of antibiotic resistance.</description><identifier>ISSN: 1460-2091</identifier><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkg398</identifier><language>eng</language><publisher>Oxford: Oxford Publishing Limited (England)</publisher><ispartof>Journal of antimicrobial chemotherapy, 2003-10, Vol.52 (4), p.623-628</ispartof><rights>Copyright Oxford University Press(England) Oct 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1039-3c678bb02e08de91fb38f1cc0b6b9d6c184674cfb761a4170e3d2391143a3f9c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Houlihan, A. J.</creatorcontrib><title>The susceptibility of ionophore-resistant Clostridium aminophilum Fto other antibiotics</title><title>Journal of antimicrobial chemotherapy</title><description>Objective: To determine if ionophore-resistant ruminal bacteria are cross-resistant to other classes of antibiotics. Clostridium aminophilum was used as a model organism because this Gram-positive ruminal bacterium can adapt to ionophores (monensin and lasalocid). Non-adapted cultures lagged for at least 12 h with 1 [mu]M monensin or lasalocid, but initiated no growth if the concentration was 10 [mu]M. Adapted cultures did not lag with 1 [mu]M monensin or lasalocid, grew well even if the ionophore concentration was 10 [mu]M and contained cells at least 100 000-fold more resistant than those in non-adapted cultures. Methods: Ionophore-adapted and non-adapted cultures were assayed for their susceptibility to other classes of antibiotics (penicillin G, ampicillin, cephalosporin C, vancomycin, carbenicillin, tetracycline, chloramphenicol, erythromycin, streptomycin, linocomycin, rifampicin, trimethoprim, novobiocin, polymyxin B and bacitracin) using a broth microdilution method. Results: Adapted cultures retained their resistance phenotype for at least 28 generations even if ionophore was no longer present. Monensin-adapted cultures were as resistant to lasalocid as those adapted to lasalocid, but lasalocid-adapted cultures lagged with 1 [mu]M monensin. Monensin- and lasalocid-resistant C. aminophilum F cultures were as susceptible to most antibiotics as non-adapted cultures. The only antibiotic that seemed to have a common mechanism of resistance was bacitracin, and the ionophore-adapted cultures had a 32-fold greater MIC. Conclusion: The use of ionophores in cattle feed and the selection of ionophore-resistant ruminal bacteria does not necessarily lead to other types of antibiotic resistance.</description><issn>1460-2091</issn><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpNkLFOwzAURS0EEqWw8AUWI1KoX15w4hFVFJAqsRQxWrZjU5e0DrYz9O9JFQame4eje6VDyC2wB2ACFztlFu33F4rmjMyg4qwomYDzf_2SXKW0Y4zxR97MyOdma2kakrF99tp3Ph9pcNSHQ-i3Idoi2uRTVodMl11IOfrWD3uq9v4E-G7sqxxoyFsb6UiNGyF7k67JhVNdsjd_OScfq-fN8rVYv7-8LZ_WhQGGokDD60ZrVlrWtFaA09g4MIZprkXLDTQVryvjdM1BVVAzi22JAqBChU4YnJO7abeP4WewKctdGOJhvJQl1JwjlmKE7ifIxJBStE720e9VPEpg8uRNjt7k5A1_AbzyYuQ</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>Houlihan, A. J.</creator><general>Oxford Publishing Limited (England)</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope></search><sort><creationdate>20031001</creationdate><title>The susceptibility of ionophore-resistant Clostridium aminophilum Fto other antibiotics</title><author>Houlihan, A. J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1039-3c678bb02e08de91fb38f1cc0b6b9d6c184674cfb761a4170e3d2391143a3f9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Houlihan, A. J.</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology 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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Houlihan, A. J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The susceptibility of ionophore-resistant Clostridium aminophilum Fto other antibiotics</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><date>2003-10-01</date><risdate>2003</risdate><volume>52</volume><issue>4</issue><spage>623</spage><epage>628</epage><pages>623-628</pages><issn>1460-2091</issn><issn>0305-7453</issn><eissn>1460-2091</eissn><abstract>Objective: To determine if ionophore-resistant ruminal bacteria are cross-resistant to other classes of antibiotics. Clostridium aminophilum was used as a model organism because this Gram-positive ruminal bacterium can adapt to ionophores (monensin and lasalocid). Non-adapted cultures lagged for at least 12 h with 1 [mu]M monensin or lasalocid, but initiated no growth if the concentration was 10 [mu]M. Adapted cultures did not lag with 1 [mu]M monensin or lasalocid, grew well even if the ionophore concentration was 10 [mu]M and contained cells at least 100 000-fold more resistant than those in non-adapted cultures. Methods: Ionophore-adapted and non-adapted cultures were assayed for their susceptibility to other classes of antibiotics (penicillin G, ampicillin, cephalosporin C, vancomycin, carbenicillin, tetracycline, chloramphenicol, erythromycin, streptomycin, linocomycin, rifampicin, trimethoprim, novobiocin, polymyxin B and bacitracin) using a broth microdilution method. Results: Adapted cultures retained their resistance phenotype for at least 28 generations even if ionophore was no longer present. Monensin-adapted cultures were as resistant to lasalocid as those adapted to lasalocid, but lasalocid-adapted cultures lagged with 1 [mu]M monensin. Monensin- and lasalocid-resistant C. aminophilum F cultures were as susceptible to most antibiotics as non-adapted cultures. The only antibiotic that seemed to have a common mechanism of resistance was bacitracin, and the ionophore-adapted cultures had a 32-fold greater MIC. Conclusion: The use of ionophores in cattle feed and the selection of ionophore-resistant ruminal bacteria does not necessarily lead to other types of antibiotic resistance.</abstract><cop>Oxford</cop><pub>Oxford Publishing Limited (England)</pub><doi>10.1093/jac/dkg398</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1460-2091 |
ispartof | Journal of antimicrobial chemotherapy, 2003-10, Vol.52 (4), p.623-628 |
issn | 1460-2091 0305-7453 1460-2091 |
language | eng |
recordid | cdi_proquest_journals_217663329 |
source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Oxford University Press Journals All Titles (1996-Current); Free Full-Text Journals in Chemistry |
title | The susceptibility of ionophore-resistant Clostridium aminophilum Fto other antibiotics |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T01%3A53%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20susceptibility%20of%20ionophore-resistant%20Clostridium%20aminophilum%20Fto%20other%20antibiotics&rft.jtitle=Journal%20of%20antimicrobial%20chemotherapy&rft.au=Houlihan,%20A.%20J.&rft.date=2003-10-01&rft.volume=52&rft.issue=4&rft.spage=623&rft.epage=628&rft.pages=623-628&rft.issn=1460-2091&rft.eissn=1460-2091&rft_id=info:doi/10.1093/jac/dkg398&rft_dat=%3Cproquest_cross%3E431326411%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=217663329&rft_id=info:pmid/&rfr_iscdi=true |