Publication:
Genetic diversity and microevolution of Burkholderia pseudomallei in the environment

dc.contributor.authorNarisara Chantratitaen_US
dc.contributor.authorVanaporn Wuthiekanunen_US
dc.contributor.authorDirek Limmathurotsakulen_US
dc.contributor.authorMongkol Vesaratchavesten_US
dc.contributor.authorAunchalee Thanwisaien_US
dc.contributor.authorPremjit Amomchaien_US
dc.contributor.authorSarinna Tumapaen_US
dc.contributor.authorEdward J. Feilen_US
dc.contributor.authorNicholas P. Dayen_US
dc.contributor.authorSharon J. Peacocken_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Bathen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.date.accessioned2018-07-12T02:46:39Z
dc.date.available2018-07-12T02:46:39Z
dc.date.issued2008-02-01en_US
dc.description.abstractBackground: The soil dwelling Gram-negative pathogen Burkholderia pseudomallei is the cause of melioidosis. The diversity and population structure of this organism in the environment is poorly defined. Methods and Findings: We undertook a study of B. pseudomallei in soil sampled from 100 equally spaced points within 237.5 m2 of disused land in northeast Thailand. B. pseudomallei was present on direct culture of 77/100 sampling points. Genotyping of 200 primary plate colonies from three independent sampling points was performed using a combination of pulsed field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). Twelve PFGE types and nine sequence types (STs) were identified, the majority of which were present at only a single sampling point. Two sampling points contained four STs and the third point contained three STs. Although the distance between the three sampling points was low (7.6, 7.9, and 13.3 meters, respectively), only two STs were present in more than one sampling point. Each of the three samples was characterized by the localized expansion of a single B. pseudomallei clone (corresponding to STs 185, 163, and 93). Comparison of PFGE and MLST results demonstrated that two STs contained strains with variable PFGE banding pattern types, indicating geographic structuring even within a single MLST-defined clone. Conclusions: We discuss the implications of this extreme structuring of genotype and genotypic frequency in terms of micro-evolutionary dynamics and ecology, and how our results may inform future sampling strategies. © 2008 Chantratita et al.en_US
dc.identifier.citationPLoS Neglected Tropical Diseases. Vol.2, No.2 (2008)en_US
dc.identifier.doi10.1371/journal.pntd.0000182en_US
dc.identifier.other2-s2.0-48949118002en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/19773
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=48949118002&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleGenetic diversity and microevolution of Burkholderia pseudomallei in the environmenten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=48949118002&origin=inwarden_US

Files

Collections