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Draft genome of a macrolide resistant XDR Salmonella enterica serovar Paratyphi A strain using a shotgun sequencing approach
Salmonella enterica serovar Paratyphi A, the causative pathogen of enteric fever, is a major public-health concern affecting millions of people around the world. We conducted whole-genome sequencing and analysis of a novel macrolide-resistant Salmonella Paratyphi A strain isolated from Karachi, Paki...
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Published in: | Journal of global antimicrobial resistance. 2019-12, Vol.19, p.129-131 |
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description | Salmonella enterica serovar Paratyphi A, the causative pathogen of enteric fever, is a major public-health concern affecting millions of people around the world. We conducted whole-genome sequencing and analysis of a novel macrolide-resistant Salmonella Paratyphi A strain isolated from Karachi, Pakistan.
Genomic DNA of Salmonella Paratyphi A strain JRCGR-AK14 was sequenced on a MiSeq platform. Read quality was evaluated and paired-end reads were assembled into contigs and scaffolds. The quality of contigs and scaffolds was evaluated and assembled contigs were annotated. Virulence genes, antimicrobial resistance genes (ARGs), tRNAs, rRNAs, coding sequences and clustered regularly interspaced short palindromic repeats (CRISPRs) were identified. ARGs and mutations in quinolone-resistance determining regions (QRDRs) were identified by Antimicrobial Resistance Identification By Assembly (ARIBA) and ResFinder. Known and unknow mutations in the QRDRs were predicted.
The genome of Salmonella Paratyphi A was calculated at 4529866 bp with 4381 genes and 1088 hypothetical proteins. Several putative genes coding for multidrug efflux pumps were identified. In addition, gene mutations conferring resistance to nitrofurantoin (e.g. marA, mdsC, Escherichia coli soxS), pulvomycin (e.g. H-NS, cpxA, E. coli EF-Tu) and fosfomycin (CRP, kdpE, E. coli glpT) were also identified. Several ARGs along with the mobile genetic element transposon Tn10 were also identified. It is evident from the results that diverse redundant mechanisms are involved in regulation of drug resistance in this strain.
The current findings provide valuable data for understanding the multidrug resistance and pathogenic characteristics of clinical Salmonella Paratyphi A isolates. |
doi_str_mv | 10.1016/j.jgar.2019.09.001 |
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Genomic DNA of Salmonella Paratyphi A strain JRCGR-AK14 was sequenced on a MiSeq platform. Read quality was evaluated and paired-end reads were assembled into contigs and scaffolds. The quality of contigs and scaffolds was evaluated and assembled contigs were annotated. Virulence genes, antimicrobial resistance genes (ARGs), tRNAs, rRNAs, coding sequences and clustered regularly interspaced short palindromic repeats (CRISPRs) were identified. ARGs and mutations in quinolone-resistance determining regions (QRDRs) were identified by Antimicrobial Resistance Identification By Assembly (ARIBA) and ResFinder. Known and unknow mutations in the QRDRs were predicted.
The genome of Salmonella Paratyphi A was calculated at 4529866 bp with 4381 genes and 1088 hypothetical proteins. Several putative genes coding for multidrug efflux pumps were identified. In addition, gene mutations conferring resistance to nitrofurantoin (e.g. marA, mdsC, Escherichia coli soxS), pulvomycin (e.g. H-NS, cpxA, E. coli EF-Tu) and fosfomycin (CRP, kdpE, E. coli glpT) were also identified. Several ARGs along with the mobile genetic element transposon Tn10 were also identified. It is evident from the results that diverse redundant mechanisms are involved in regulation of drug resistance in this strain.
The current findings provide valuable data for understanding the multidrug resistance and pathogenic characteristics of clinical Salmonella Paratyphi A isolates.</description><identifier>ISSN: 2213-7165</identifier><identifier>EISSN: 2213-7173</identifier><identifier>DOI: 10.1016/j.jgar.2019.09.001</identifier><identifier>PMID: 31505298</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Enteric fever ; Macrolide resistance ; Multidrug resistance ; Salmonella Paratyphi A ; Whole-genome sequencing</subject><ispartof>Journal of global antimicrobial resistance., 2019-12, Vol.19, p.129-131</ispartof><rights>2019 International Society for Antimicrobial Chemotherapy</rights><rights>Copyright © 2019 International Society for Antimicrobial Chemotherapy. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-3b16c5bfc34218a92c0242c2193c7d689bd9dee100bef64e529e6bfeb0f123ae3</citedby><cites>FETCH-LOGICAL-c400t-3b16c5bfc34218a92c0242c2193c7d689bd9dee100bef64e529e6bfeb0f123ae3</cites><orcidid>0000-0002-7309-4541 ; 0000-0002-8064-0651</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2213716519302334$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31505298$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khatoon, A.</creatorcontrib><creatorcontrib>Malik, H.M.T.</creatorcontrib><creatorcontrib>Aurongzeb, M.</creatorcontrib><creatorcontrib>Raza, S.A.</creatorcontrib><creatorcontrib>Karim, A.</creatorcontrib><title>Draft genome of a macrolide resistant XDR Salmonella enterica serovar Paratyphi A strain using a shotgun sequencing approach</title><title>Journal of global antimicrobial resistance.</title><addtitle>J Glob Antimicrob Resist</addtitle><description>Salmonella enterica serovar Paratyphi A, the causative pathogen of enteric fever, is a major public-health concern affecting millions of people around the world. We conducted whole-genome sequencing and analysis of a novel macrolide-resistant Salmonella Paratyphi A strain isolated from Karachi, Pakistan.
Genomic DNA of Salmonella Paratyphi A strain JRCGR-AK14 was sequenced on a MiSeq platform. Read quality was evaluated and paired-end reads were assembled into contigs and scaffolds. The quality of contigs and scaffolds was evaluated and assembled contigs were annotated. Virulence genes, antimicrobial resistance genes (ARGs), tRNAs, rRNAs, coding sequences and clustered regularly interspaced short palindromic repeats (CRISPRs) were identified. ARGs and mutations in quinolone-resistance determining regions (QRDRs) were identified by Antimicrobial Resistance Identification By Assembly (ARIBA) and ResFinder. Known and unknow mutations in the QRDRs were predicted.
The genome of Salmonella Paratyphi A was calculated at 4529866 bp with 4381 genes and 1088 hypothetical proteins. Several putative genes coding for multidrug efflux pumps were identified. In addition, gene mutations conferring resistance to nitrofurantoin (e.g. marA, mdsC, Escherichia coli soxS), pulvomycin (e.g. H-NS, cpxA, E. coli EF-Tu) and fosfomycin (CRP, kdpE, E. coli glpT) were also identified. Several ARGs along with the mobile genetic element transposon Tn10 were also identified. It is evident from the results that diverse redundant mechanisms are involved in regulation of drug resistance in this strain.
The current findings provide valuable data for understanding the multidrug resistance and pathogenic characteristics of clinical Salmonella Paratyphi A isolates.</description><subject>Enteric fever</subject><subject>Macrolide resistance</subject><subject>Multidrug resistance</subject><subject>Salmonella Paratyphi A</subject><subject>Whole-genome sequencing</subject><issn>2213-7165</issn><issn>2213-7173</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kF9LXDEQxUNpqWL9Aj5IHn3Z7SS5f8EX0VYLQqVa8C3MzZ27m-XeZE1yBcEP32zX-tgwkDCcOZnzY-xEwFKAqL5ulpsVhqUE0S4hF4gP7FBKoRa1qNXH93dVHrDjGDeQT1sIWdWf2YESJZSybQ7Z61XAIfEVOT8R9wNHPqEJfrQ98UDRxoQu8cerX_wex8k7Gkfk5BIFa5BHCv4ZA7_DgOllu7b8gscU0Do-R-tW2S6ufVrNLkufZnLmb3O7DR7N-gv7NOAY6fjtPmK_v397uLxZ3P68_nF5cbswBUBaqE5UpuwGowopGmylAVlII0WrTN1XTdv1bU8kADoaqoJyMqq6gToYhFRI6oid7X3zt3mJmPRko9klceTnqKVsmrqUqoIslXtpZhBjoEFvg50wvGgBegdeb_QOvN6B15ALRB46ffOfu4n695F_mLPgfC-gnPLZUtDR2AyDehvIJN17-z__P9ZvlgQ</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Khatoon, A.</creator><creator>Malik, H.M.T.</creator><creator>Aurongzeb, M.</creator><creator>Raza, S.A.</creator><creator>Karim, A.</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7309-4541</orcidid><orcidid>https://orcid.org/0000-0002-8064-0651</orcidid></search><sort><creationdate>201912</creationdate><title>Draft genome of a macrolide resistant XDR Salmonella enterica serovar Paratyphi A strain using a shotgun sequencing approach</title><author>Khatoon, A. ; Malik, H.M.T. ; Aurongzeb, M. ; Raza, S.A. ; Karim, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-3b16c5bfc34218a92c0242c2193c7d689bd9dee100bef64e529e6bfeb0f123ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Enteric fever</topic><topic>Macrolide resistance</topic><topic>Multidrug resistance</topic><topic>Salmonella Paratyphi A</topic><topic>Whole-genome sequencing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khatoon, A.</creatorcontrib><creatorcontrib>Malik, H.M.T.</creatorcontrib><creatorcontrib>Aurongzeb, M.</creatorcontrib><creatorcontrib>Raza, S.A.</creatorcontrib><creatorcontrib>Karim, A.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of global antimicrobial resistance.</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khatoon, A.</au><au>Malik, H.M.T.</au><au>Aurongzeb, M.</au><au>Raza, S.A.</au><au>Karim, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Draft genome of a macrolide resistant XDR Salmonella enterica serovar Paratyphi A strain using a shotgun sequencing approach</atitle><jtitle>Journal of global antimicrobial resistance.</jtitle><addtitle>J Glob Antimicrob Resist</addtitle><date>2019-12</date><risdate>2019</risdate><volume>19</volume><spage>129</spage><epage>131</epage><pages>129-131</pages><issn>2213-7165</issn><eissn>2213-7173</eissn><abstract>Salmonella enterica serovar Paratyphi A, the causative pathogen of enteric fever, is a major public-health concern affecting millions of people around the world. We conducted whole-genome sequencing and analysis of a novel macrolide-resistant Salmonella Paratyphi A strain isolated from Karachi, Pakistan.
Genomic DNA of Salmonella Paratyphi A strain JRCGR-AK14 was sequenced on a MiSeq platform. Read quality was evaluated and paired-end reads were assembled into contigs and scaffolds. The quality of contigs and scaffolds was evaluated and assembled contigs were annotated. Virulence genes, antimicrobial resistance genes (ARGs), tRNAs, rRNAs, coding sequences and clustered regularly interspaced short palindromic repeats (CRISPRs) were identified. ARGs and mutations in quinolone-resistance determining regions (QRDRs) were identified by Antimicrobial Resistance Identification By Assembly (ARIBA) and ResFinder. Known and unknow mutations in the QRDRs were predicted.
The genome of Salmonella Paratyphi A was calculated at 4529866 bp with 4381 genes and 1088 hypothetical proteins. Several putative genes coding for multidrug efflux pumps were identified. In addition, gene mutations conferring resistance to nitrofurantoin (e.g. marA, mdsC, Escherichia coli soxS), pulvomycin (e.g. H-NS, cpxA, E. coli EF-Tu) and fosfomycin (CRP, kdpE, E. coli glpT) were also identified. Several ARGs along with the mobile genetic element transposon Tn10 were also identified. It is evident from the results that diverse redundant mechanisms are involved in regulation of drug resistance in this strain.
The current findings provide valuable data for understanding the multidrug resistance and pathogenic characteristics of clinical Salmonella Paratyphi A isolates.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>31505298</pmid><doi>10.1016/j.jgar.2019.09.001</doi><tpages>3</tpages><orcidid>https://orcid.org/0000-0002-7309-4541</orcidid><orcidid>https://orcid.org/0000-0002-8064-0651</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Enteric fever Macrolide resistance Multidrug resistance Salmonella Paratyphi A Whole-genome sequencing |
title | Draft genome of a macrolide resistant XDR Salmonella enterica serovar Paratyphi A strain using a shotgun sequencing approach |
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