Publication: Molecular detection and speciation of pathogenic Leptospira spp. in blood from patients with culture-negative leptospirosis
dc.contributor.author | Siriphan Boonsilp | en_US |
dc.contributor.author | Janjira Thaipadungpanit | en_US |
dc.contributor.author | Premjit Amornchai | en_US |
dc.contributor.author | Vanaporn Wuthiekanun | en_US |
dc.contributor.author | Wirongrong Chierakul | en_US |
dc.contributor.author | Direk Limmathurotsakul | en_US |
dc.contributor.author | Nicholas P. Day | en_US |
dc.contributor.author | Sharon J. Peacock | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Faculty of Medicine, Siriraj Hospital, Mahidol University | en_US |
dc.contributor.other | Nuffield Department of Clinical Medicine | en_US |
dc.contributor.other | University of Cambridge | en_US |
dc.date.accessioned | 2018-05-03T08:20:42Z | |
dc.date.available | 2018-05-03T08:20:42Z | |
dc.date.issued | 2011-12-13 | en_US |
dc.description.abstract | Background: 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. © 2011 Boonsilp et al; licensee BioMed Central Ltd. | en_US |
dc.identifier.citation | BMC Infectious Diseases. Vol.11, (2011) | en_US |
dc.identifier.doi | 10.1186/1471-2334-11-338 | en_US |
dc.identifier.issn | 14712334 | en_US |
dc.identifier.other | 2-s2.0-83255164933 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/12153 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=83255164933&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Molecular detection and speciation of pathogenic Leptospira spp. in blood from patients with culture-negative leptospirosis | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=83255164933&origin=inward | en_US |