Alterations of Salmonella enterica Serovar Typhimurium Antibiotic Resistance under Environmental Pressure
Microbial horizontal gene transfer is a continuous process that shapes bacterial genomic adaptation to the environment and the composition of concurrent microbial ecology. This includes the potential impact of synthetic antibiotic utilization in farm animal production on overall antibiotic resistanc...
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description | Microbial horizontal gene transfer is a continuous process that shapes bacterial genomic adaptation to the environment and the composition of concurrent microbial ecology. This includes the potential impact of synthetic antibiotic utilization in farm animal production on overall antibiotic resistance issues; however, the mechanisms behind the evolution of microbial communities are not fully understood. We explored potential mechanisms by experimentally examining the relatedness of phylogenetic inference between multidrug-resistant
serovar Typhimurium isolates and pathogenic
Typhimurium strains based on genome-wide single-nucleotide polymorphism (SNP) comparisons. Antibiotic-resistant
Typhimurium isolates in a simulated farm environment barely lost their resistance, whereas sensitive
Typhimurium isolates in soils gradually acquired higher tetracycline resistance under antibiotic pressure and manipulated differential expression of antibiotic-resistant genes. The expeditious development of antibiotic resistance and the ensuing genetic alterations in antimicrobial resistance genes in
Typhimurium warrant effective actions to control the dissemination of
antibiotic resistance.
Antibiotic resistance is attributed to the misuse or overuse of antibiotics in agriculture, and antibiotic resistance genes can also be transferred to bacteria under environmental stress. In this study, we report a unidirectional alteration in antibiotic resistance from susceptibility to increased resistance. Highly sensitive
serovar Typhimurium isolates from organic farm systems quickly acquired tetracycline resistance under antibiotic pressure in simulated farm soil environments within 2 weeks, with expression of antibiotic resistance-related genes that was significantly upregulated. Conversely, originally resistant
Typhimurium isolates from conventional farm systems lost little of their resistance when transferred to environments without antibiotic pressure. Additionally, multidrug-resistant
Typhimurium isolates genetically shared relevancy with pathogenic
Typhimurium isolates, whereas susceptible isolates clustered with nonpathogenic strains. These results provide detailed discussion and explanation about the genetic alterations and simultaneous acquisition of antibiotic resistance in
Typhimurium in agricultural environments. |
doi_str_mv | 10.1128/AEM.01173-18 |
format | Article |
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serovar Typhimurium isolates and pathogenic
Typhimurium strains based on genome-wide single-nucleotide polymorphism (SNP) comparisons. Antibiotic-resistant
Typhimurium isolates in a simulated farm environment barely lost their resistance, whereas sensitive
Typhimurium isolates in soils gradually acquired higher tetracycline resistance under antibiotic pressure and manipulated differential expression of antibiotic-resistant genes. The expeditious development of antibiotic resistance and the ensuing genetic alterations in antimicrobial resistance genes in
Typhimurium warrant effective actions to control the dissemination of
antibiotic resistance.
Antibiotic resistance is attributed to the misuse or overuse of antibiotics in agriculture, and antibiotic resistance genes can also be transferred to bacteria under environmental stress. In this study, we report a unidirectional alteration in antibiotic resistance from susceptibility to increased resistance. Highly sensitive
serovar Typhimurium isolates from organic farm systems quickly acquired tetracycline resistance under antibiotic pressure in simulated farm soil environments within 2 weeks, with expression of antibiotic resistance-related genes that was significantly upregulated. Conversely, originally resistant
Typhimurium isolates from conventional farm systems lost little of their resistance when transferred to environments without antibiotic pressure. Additionally, multidrug-resistant
Typhimurium isolates genetically shared relevancy with pathogenic
Typhimurium isolates, whereas susceptible isolates clustered with nonpathogenic strains. These results provide detailed discussion and explanation about the genetic alterations and simultaneous acquisition of antibiotic resistance in
Typhimurium in agricultural environments.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>DOI: 10.1128/AEM.01173-18</identifier><identifier>PMID: 30054356</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Animal production ; Antibiotic resistance ; Antibiotics ; Antimicrobial resistance ; Drug resistance ; Farms ; Gene expression ; Gene transfer ; Genes ; Genomes ; Microbial activity ; Microorganisms ; Multidrug resistance ; Phylogeny ; Polymorphism ; Pressure ; Public and Environmental Health Microbiology ; Salmonella ; Salmonella enterica ; Single-nucleotide polymorphism</subject><ispartof>Applied and environmental microbiology, 2018-10, Vol.84 (19)</ispartof><rights>Copyright © 2018 American Society for Microbiology.</rights><rights>Copyright American Society for Microbiology Oct 2018</rights><rights>Copyright © 2018 American Society for Microbiology. 2018 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-df0212297a40eed2fdcdee1106520f9703d444d9dc09c7bb02ec0f2279fb49683</citedby><cites>FETCH-LOGICAL-c412t-df0212297a40eed2fdcdee1106520f9703d444d9dc09c7bb02ec0f2279fb49683</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/PMC6146977/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6146977/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30054356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Schaffner, Donald W.</contributor><creatorcontrib>Peng, Mengfei</creatorcontrib><creatorcontrib>Salaheen, Serajus</creatorcontrib><creatorcontrib>Buchanan, Robert L</creatorcontrib><creatorcontrib>Biswas, Debabrata</creatorcontrib><title>Alterations of Salmonella enterica Serovar Typhimurium Antibiotic Resistance under Environmental Pressure</title><title>Applied and environmental microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Microbial horizontal gene transfer is a continuous process that shapes bacterial genomic adaptation to the environment and the composition of concurrent microbial ecology. This includes the potential impact of synthetic antibiotic utilization in farm animal production on overall antibiotic resistance issues; however, the mechanisms behind the evolution of microbial communities are not fully understood. We explored potential mechanisms by experimentally examining the relatedness of phylogenetic inference between multidrug-resistant
serovar Typhimurium isolates and pathogenic
Typhimurium strains based on genome-wide single-nucleotide polymorphism (SNP) comparisons. Antibiotic-resistant
Typhimurium isolates in a simulated farm environment barely lost their resistance, whereas sensitive
Typhimurium isolates in soils gradually acquired higher tetracycline resistance under antibiotic pressure and manipulated differential expression of antibiotic-resistant genes. The expeditious development of antibiotic resistance and the ensuing genetic alterations in antimicrobial resistance genes in
Typhimurium warrant effective actions to control the dissemination of
antibiotic resistance.
Antibiotic resistance is attributed to the misuse or overuse of antibiotics in agriculture, and antibiotic resistance genes can also be transferred to bacteria under environmental stress. In this study, we report a unidirectional alteration in antibiotic resistance from susceptibility to increased resistance. Highly sensitive
serovar Typhimurium isolates from organic farm systems quickly acquired tetracycline resistance under antibiotic pressure in simulated farm soil environments within 2 weeks, with expression of antibiotic resistance-related genes that was significantly upregulated. Conversely, originally resistant
Typhimurium isolates from conventional farm systems lost little of their resistance when transferred to environments without antibiotic pressure. Additionally, multidrug-resistant
Typhimurium isolates genetically shared relevancy with pathogenic
Typhimurium isolates, whereas susceptible isolates clustered with nonpathogenic strains. These results provide detailed discussion and explanation about the genetic alterations and simultaneous acquisition of antibiotic resistance in
Typhimurium in agricultural environments.</description><subject>Animal production</subject><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Antimicrobial resistance</subject><subject>Drug resistance</subject><subject>Farms</subject><subject>Gene expression</subject><subject>Gene transfer</subject><subject>Genes</subject><subject>Genomes</subject><subject>Microbial activity</subject><subject>Microorganisms</subject><subject>Multidrug resistance</subject><subject>Phylogeny</subject><subject>Polymorphism</subject><subject>Pressure</subject><subject>Public and Environmental Health Microbiology</subject><subject>Salmonella</subject><subject>Salmonella enterica</subject><subject>Single-nucleotide polymorphism</subject><issn>0099-2240</issn><issn>1098-5336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdkc1v1DAUxC0EokvhxhlZ4tIDKc8fseML0qpaaKVWRbScLcd5oa4Se7GTlfrfk6Wlajm9w_w0mnlDyHsGx4zx5vN6c3EMjGlRseYFWTEwTVULoV6SFYAxFecSDsibUm4BQIJqXpMDAVBLUasVCethwuymkGKhqadXbhhTxGFwFOOiBO_oFea0c5le321vwjjnMI90HafQhjQFT39gCWVy0SOdY4eZbuIu5BTHxcAN9HvGUuaMb8mr3g0F3z3cQ_Lz6-b65LQ6v_x2drI-r7xkfKq6Hjjj3GgnAbHjfec7RMZA1Rx6o0F0UsrOdB6M120LHD30nGvTt9KoRhySL_e-27kdsfNLiuwGu81hdPnOJhfscyWGG_sr7axiUhmtF4OjB4Ocfs9YJjuG4vcviZjmYjnopm6EELCgH_9Db9Oc41LPLiVqrUCqeqE-3VM-p1Iy9o9hGNj9hnbZ0P7d0LJ9gQ9PCzzC_0YTfwCq4ZmU</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Peng, Mengfei</creator><creator>Salaheen, Serajus</creator><creator>Buchanan, Robert L</creator><creator>Biswas, Debabrata</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20181001</creationdate><title>Alterations of Salmonella enterica Serovar Typhimurium Antibiotic Resistance under Environmental Pressure</title><author>Peng, Mengfei ; Salaheen, Serajus ; Buchanan, Robert L ; Biswas, Debabrata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-df0212297a40eed2fdcdee1106520f9703d444d9dc09c7bb02ec0f2279fb49683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animal production</topic><topic>Antibiotic resistance</topic><topic>Antibiotics</topic><topic>Antimicrobial resistance</topic><topic>Drug resistance</topic><topic>Farms</topic><topic>Gene expression</topic><topic>Gene transfer</topic><topic>Genes</topic><topic>Genomes</topic><topic>Microbial activity</topic><topic>Microorganisms</topic><topic>Multidrug resistance</topic><topic>Phylogeny</topic><topic>Polymorphism</topic><topic>Pressure</topic><topic>Public and Environmental Health Microbiology</topic><topic>Salmonella</topic><topic>Salmonella enterica</topic><topic>Single-nucleotide polymorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, Mengfei</creatorcontrib><creatorcontrib>Salaheen, Serajus</creatorcontrib><creatorcontrib>Buchanan, Robert L</creatorcontrib><creatorcontrib>Biswas, Debabrata</creatorcontrib><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>Peng, Mengfei</au><au>Salaheen, Serajus</au><au>Buchanan, Robert L</au><au>Biswas, Debabrata</au><au>Schaffner, Donald W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alterations of Salmonella enterica Serovar Typhimurium Antibiotic Resistance under Environmental Pressure</atitle><jtitle>Applied and environmental microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2018-10-01</date><risdate>2018</risdate><volume>84</volume><issue>19</issue><issn>0099-2240</issn><eissn>1098-5336</eissn><abstract>Microbial horizontal gene transfer is a continuous process that shapes bacterial genomic adaptation to the environment and the composition of concurrent microbial ecology. This includes the potential impact of synthetic antibiotic utilization in farm animal production on overall antibiotic resistance issues; however, the mechanisms behind the evolution of microbial communities are not fully understood. We explored potential mechanisms by experimentally examining the relatedness of phylogenetic inference between multidrug-resistant
serovar Typhimurium isolates and pathogenic
Typhimurium strains based on genome-wide single-nucleotide polymorphism (SNP) comparisons. Antibiotic-resistant
Typhimurium isolates in a simulated farm environment barely lost their resistance, whereas sensitive
Typhimurium isolates in soils gradually acquired higher tetracycline resistance under antibiotic pressure and manipulated differential expression of antibiotic-resistant genes. The expeditious development of antibiotic resistance and the ensuing genetic alterations in antimicrobial resistance genes in
Typhimurium warrant effective actions to control the dissemination of
antibiotic resistance.
Antibiotic resistance is attributed to the misuse or overuse of antibiotics in agriculture, and antibiotic resistance genes can also be transferred to bacteria under environmental stress. In this study, we report a unidirectional alteration in antibiotic resistance from susceptibility to increased resistance. Highly sensitive
serovar Typhimurium isolates from organic farm systems quickly acquired tetracycline resistance under antibiotic pressure in simulated farm soil environments within 2 weeks, with expression of antibiotic resistance-related genes that was significantly upregulated. Conversely, originally resistant
Typhimurium isolates from conventional farm systems lost little of their resistance when transferred to environments without antibiotic pressure. Additionally, multidrug-resistant
Typhimurium isolates genetically shared relevancy with pathogenic
Typhimurium isolates, whereas susceptible isolates clustered with nonpathogenic strains. These results provide detailed discussion and explanation about the genetic alterations and simultaneous acquisition of antibiotic resistance in
Typhimurium in agricultural environments.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>30054356</pmid><doi>10.1128/AEM.01173-18</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animal production Antibiotic resistance Antibiotics Antimicrobial resistance Drug resistance Farms Gene expression Gene transfer Genes Genomes Microbial activity Microorganisms Multidrug resistance Phylogeny Polymorphism Pressure Public and Environmental Health Microbiology Salmonella Salmonella enterica Single-nucleotide polymorphism |
title | Alterations of Salmonella enterica Serovar Typhimurium Antibiotic Resistance under Environmental Pressure |
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