Publication:
Molecular detection and speciation of pathogenic Leptospira spp. in blood from patients with culture-negative leptospirosis

dc.contributor.authorSiriphan Boonsilpen_US
dc.contributor.authorJanjira Thaipadungpaniten_US
dc.contributor.authorจันทร์จิรา ไทยผดุงพานิชen_US
dc.contributor.authorPremjit Amornchaien_US
dc.contributor.authorเปรมจิตต์ อมรชัยen_US
dc.contributor.authorVanaporn Wuthiekanunen_US
dc.contributor.authorWirongrong Chierakulen_US
dc.contributor.authorDirek Limmathurotsakulen_US
dc.contributor.authorดิเรก ลิ้มมธุรสกุลen_US
dc.contributor.authorDay, Nicholas P.en_US
dc.contributor.authorPeacock, Sharon J.en_US
dc.contributor.correspondenceJanjira Thaipadungpanit
dc.contributor.otherMahidol University. Faculty of Tropical Medicine. Mahidol-Oxford Tropical Medicine Research Unit
dc.date.accessioned2012-10-11T04:32:11Z
dc.date.accessioned2016-09-29T15:36:19Z
dc.date.available2012-10-11T04:32:11Z
dc.date.available2016-09-29T15:36:19Z
dc.date.copyright2011
dc.date.created2012-10-11
dc.date.issued2011-12-13
dc.description.abstractBACKGROUND: Pathogenic Leptospira spp. present in the blood of patients with leptospirosis during the first week of symptoms can be detected using culture or PCR. A proportion of patients who are positive by PCR are negative by culture. Leptospira spp. are fastidious bacteria, and we hypothesized that a false-negative culture result may represent infection with a distinct bacterial subset that fail to grow in standard culture medium. METHODS: We evaluated our hypothesis during a prospective study of 418 consecutive patients presenting to a hospital in northeast Thailand with an acute febrile illness. Admission blood samples were taken for Leptospira culture and PCR. A single tube nested PCR that amplified a region of the rrs gene was developed and applied, amplicons sequenced and a phylogenetic tree reconstructed. RESULTS: 39/418 (9%) patients were culture-positive for Leptospira spp., and 81/418 (19%) patients were culture-negative but rrs PCR-positive. The species associated with culture-positive leptospirosis (37 L. interrogans and 2 L. borgpetersenii) were comparable to those associated with culture-negative, PCR-positive leptospirosis (76 L. interrogans, 4 L. borgpetersenii, 1 unidentified, possibly new species). CONCLUSION: Molecular speciation failed to identify a unique bacterial subset in patients with culture-negative, PCR-positive leptospirosis. The rate of false-negative culture was high, and we speculate that antibiotic pre-treatment is the most likely explanation for this.en_US
dc.identifier.citationBoonsilp S, Thaipadungpanit J, Amornchai P, Wuthiekanun V, Chierakul W, Limmathurotsakul D, et al. Molecular detection and speciation of pathogenic Leptospira spp. in blood from patients with culture-negative leptospirosis. BMC Infect Dis. 2011 Dec 13;11:338.en_US
dc.identifier.doi10.1186/1471-2334-11-338
dc.identifier.issn1471-2334 (electronic)
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/740
dc.language.isoengen_US
dc.rightsMahidol Universityen_US
dc.rights.holderBMC infectious diseases
dc.subjectBacterial typing techniquesen_US
dc.subjectDNA, bacterialen_US
dc.subjectLeptospiraen_US
dc.subjectProspective studiesen_US
dc.subjectOpen Access articleen_US
dc.titleMolecular detection and speciation of pathogenic Leptospira spp. in blood from patients with culture-negative leptospirosisen_US
dc.typeResearch Articleen_US
dcterms.dateAccepted2011-12-13
dspace.entity.typePublication
mods.location.urlhttp://www.biomedcentral.com/content/pdf/1471-2334-11-338.pdf

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