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   Epidemiological tracking and population assignment of the non-clonal bacterium,burkholderia pseudomallei  
   
نویسنده dale j. ,price e.p. ,hornstra h. ,busch j.d. ,mayo m. ,godoy d. ,wuthiekanun v. ,baker a. ,foster j.t. ,wagner d.m. ,tuanyok a. ,warner j. ,spratt b.g. ,peacock s.j. ,currie b.j. ,keim p. ,pearson t.
منبع plos neglected tropical diseases - 2011 - دوره : 5 - شماره : 12
چکیده    Rapid assignment of bacterial pathogens into predefined populations is an important first step for epidemiological tracking. for clonal species,a single allele can theoretically define a population. for non-clonal species such as burkholderia pseudomallei,however,shared allelic states between distantly related isolates make it more difficult to identify population defining characteristics. two distinct b. pseudomallei populations have been previously identified using multilocus sequence typing (mlst). these populations correlate with the major foci of endemicity (australia and southeast asia). here,we use multiple bayesian approaches to evaluate the compositional robustness of these populations,and provide assignment results for mlst sequence types (sts). our goal was to provide a reference for assigning sts to an established population without the need for further computational analyses. we also provide allele frequency results for each population to enable estimation of population assignment even when novel sts are discovered. the ability for humans and potentially contaminated goods to move rapidly across the globe complicates the task of identifying the source of an infection or outbreak. population genetic dynamics of b. pseudomallei are particularly complicated relative to other bacterial pathogens,but the work here provides the ability for broad scale population assignment. as there is currently no independent empirical measure of successful population assignment,we provide comprehensive analytical details of our comparisons to enable the reader to evaluate the robustness of population designations and assignments as they pertain to individual research questions. finer scale subdivision and verification of current population compositions will likely be possible with genotyping data that more comprehensively samples the genome. the approach used here may be valuable for other non-clonal pathogens that lack simple group-defining genetic characteristics and provides a rapid reference for epidemiologists wishing to track the origin of infection without the need to compile population data and learn population assignment algorithms. © 2011 dale et al.
آدرس center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States, center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States, center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States, center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States, menzies school of health research and northern territory clinical school,royal darwin hospital,darwin,nt, Australia, department of infectious disease epidemiology,imperial college london,london, United Kingdom, mahidol-oxford tropical medicine research unit,faculty of tropical medicine,mahidol university,bangkok, Thailand, microbiology and immunology,school of veterinary and biomedical sciences,james cook university,townsville,qld, Australia, center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States, center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States, center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States, microbiology and immunology,school of veterinary and biomedical sciences,james cook university,townsville,qld, Australia, department of infectious disease epidemiology,imperial college london,london, United Kingdom, mahidol-oxford tropical medicine research unit,faculty of tropical medicine,mahidol university,bangkok,thailand,department of microbiology and immunology,faculty of tropical medicine,mahidol university,bangkok,thailand,department of medicine,university of cambridge,cambridge, United Kingdom, menzies school of health research and northern territory clinical school,royal darwin hospital,darwin,nt, Australia, center for microbial genetics and genomics,northern arizona university,flagstaff,az,united states,pathogen genomics division,translational genomics research institute,phoenix,az, United States, center for microbial genetics and genomics,northern arizona university,flagstaff,az, United States
 
     
   
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