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   Emergence of a globally dominant inchi1 plasmid type associated with multiple drug resistant typhoid  
   
نویسنده holt k.e. ,phan m.d. ,baker s. ,duy p.t. ,nga t.v.t. ,nair s. ,turner a.k. ,walsh c. ,fanning s. ,farrell-ward s. ,dutta s. ,kariuki s. ,weillfranç f.-x. ,parkhill j. ,dougan g. ,wain j.
منبع plos neglected tropical diseases - 2011 - دوره : 5 - شماره : 7
چکیده    Typhoid fever,caused by salmonella enterica serovar typhi (s. typhi),remains a serious global health concern. since their emergence in the mid-1970s multi-drug resistant (mdr) s. typhi now dominate drug sensitive equivalents in many regions. mdr in s. typhi is almost exclusively conferred by self-transmissible inchi1 plasmids carrying a suite of antimicrobial resistance genes. we identified over 300 single nucleotide polymorphisms (snps) within conserved regions of the inchi1 plasmid,and genotyped both plasmid and chromosomal snps in over 450 s. typhi dating back to 1958. prior to 1995,a variety of inchi1 plasmid types were detected in distinct s. typhi haplotypes. highly similar plasmids were detected in co-circulating s. typhi haplotypes,indicative of plasmid transfer. in contrast,from 1995 onwards,98% of mdr s. typhi were plasmid sequence type 6 (pst6) and s. typhi haplotype h58,indicating recent global spread of a dominant mdr clone. to investigate whether pst6 conferred a selective advantage compared to other inchi1 plasmids,we used a phenotyping array to compare the impact of inchi1 pst6 and pst1 plasmids in a common s. typhi host. the pst6 plasmid conferred the ability to grow in high salt medium (4.7% nacl),which we demonstrate is due to the presence in pst6 of the tn6062 transposon encoding betu. © 2011 holt et al.
آدرس wellcome trust sanger institute,hinxton,cambridge,united kingdom,department of microbiology and immunology,university of melbourne,melbourne, Australia, wellcome trust sanger institute,hinxton,cambridge,united kingdom,school of chemistry and molecular biosciences,australian infectious diseases research centre,university of queensland,brisbane,qld, Australia, oxford university clinical research unit,wellcome trust major overseas programme,the hospital for tropical diseases,ho chi minh city, Viet Nam, oxford university clinical research unit,wellcome trust major overseas programme,the hospital for tropical diseases,ho chi minh city, Viet Nam, oxford university clinical research unit,wellcome trust major overseas programme,the hospital for tropical diseases,ho chi minh city, Viet Nam, laboratory of enteric pathogens,health protection agency,colindale, United Kingdom, wellcome trust sanger institute,hinxton,cambridge, United Kingdom, food safety authority of ireland,dublin, Ireland, school of public health,physiotherapy and population science,ucd centre for food safety,veterinary sciences centre,university college dublin,belfield,dublin, Ireland, school of public health,physiotherapy and population science,ucd centre for food safety,veterinary sciences centre,university college dublin,belfield,dublin, Ireland, national institute of cholera and enteric diseases,kolkata, India, kenya medical research institute,nairobi, Kenya, institut pasteur,unité des bactéries pathogènes entériques,paris, France, wellcome trust sanger institute,hinxton,cambridge, United Kingdom, wellcome trust sanger institute,hinxton,cambridge, United Kingdom, laboratory of enteric pathogens,health protection agency,colindale, United Kingdom
 
     
   
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