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   Bacterial Factors Associated with Lethal Outcome of Enteropathogenic Escherichia coli Infection: Genomic Case-Control Studies  
   
نویسنده donnenberg m.s. ,hazen t.h. ,farag t.h. ,panchalingam s. ,antonio m. ,hossain a. ,mandomando i. ,ochieng j.b. ,ramamurthy t. ,tamboura b. ,zaidi a. ,levine m.m. ,kotloff k. ,rasko d.a. ,nataro j.p.
منبع plos neglected tropical diseases - 2015 - دوره : 9 - شماره : 5
چکیده    Typical enteropathogenic escherichia coli (tepec) strains were associated with mortality in the global enteric multicenter study (gems). genetic differences in tepec strains could underlie some of the variability in clinical outcome. we produced draft genome sequences of all available tepec strains from gems lethal infections (lis) and of closely matched epec strains from gems subjects with non-lethal symptomatic infections (nsis) and asymptomatic infections (ais) to identify gene clusters (potential protein encoding sequences sharing ≥90% nucleotide sequence identity) associated with lethality. among 14,412 gene clusters identified,the presence or absence of 392 was associated with clinical outcome. as expected,more gene clusters were associated with li versus ai than li versus nsi. the gene clusters more prevalent in strains from li than those from nsi and ai included those encoding proteins involved in o-antigen biogenesis,while clusters encoding type 3 secretion effectors espj and ospb were among those more prevalent in strains from non-lethal infections. one gene cluster encoding a variant of an nleg ubiquitin ligase was associated with li versus ai,while two other nleg clusters had the opposite association. similar associations were found for two nleg gene clusters in an additional,larger sample of nsi and ai gems strains. particular genes are associated with lethal tepec infections. further study of these factors holds potential to unravel the mechanisms underlying severe disease and to prevent adverse outcomes. © 2015 donnenberg et al.
آدرس department of medicine,university of maryland school of medicine,baltimore,md, United States, institute for genome sciences,department of microbiology and immunology,university of maryland school of medicine,baltimore,md, United States, department of medicine,university of maryland school of medicine,baltimore,md, United States, center for vaccine development,university of maryland school of medicine,baltimore,md, United States, medical research council,fajara, Gambia, international center for diarrhoeal disease research,dhaka, Bangladesh, centro de investigacao em saude de manhica,maputo, Mozambique, kenya medical research institute/center for disease control,kisumu, Kenya, national institute of cholera and enteric diseases,kolkata, India, center for vaccine development—mali,bamako, Mali, the aga khan university,karachi, Pakistan, center for vaccine development,university of maryland school of medicine,baltimore,md, United States, center for vaccine development,university of maryland school of medicine,baltimore,md, United States, institute for genome sciences,department of microbiology and immunology,university of maryland school of medicine,baltimore,md, United States, department of pediatrics,university of virginia school of medicine,charlottesville,va, United States
 
     
   
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