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Optimization of culture protocols to isolate Leptospira spp. From environmental water, field investigation, and identification of factors associated with the presence of Leptospira spp. From the environment

dc.contributor.authorUdomsak Narkkulen_US
dc.contributor.authorJanjira Thaipadungpaniten_US
dc.contributor.authorJanjira Thaipadungpaniten_US
dc.contributor.authorPrapaporn Srilohasinen_US
dc.contributor.authorPreeraya Singkhaimuken_US
dc.contributor.authorMetawee Thongdeeen_US
dc.contributor.authorSomjit Chaiwattanarungruengpaisanen_US
dc.contributor.authorPanadda Krairojanananen_US
dc.contributor.authorWirichada Pan-Ngumen_US
dc.contributor.otherArmed Forces Research Institute of Medical Sciences, Thailanden_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.date.accessioned2020-08-25T10:06:11Z
dc.date.available2020-08-25T10:06:11Z
dc.date.issued2020-06-01en_US
dc.description.abstract© 2020 by the authors. The successful culture of Leptospira spp. from the environment is challenging. Here, we optimized the isolation of Leptospira spp. from water samples spiked with different species and initial concentrations of this organism. The time periods between water sampling and the isolation process were varied (0, 2, and 4 weeks). Bacterial cultures were observed under a microscope, and cultures were graded for cell density, weekly, for 12 weeks. Most pathogenic Leptospira spp. were difficult to culture under all conditions. All conditions of water samples spiked with novel species of Leptospira subclade P1 were culture positive within 2 weeks. For Leptospira subclade P2, storing samples for 2 weeks prior to isolation resulted in more successful isolation compared with isolation after other storage conditions. For subclade S1, all samples with initial bacterial concentrations of more than 103 colonies/mL, under all storage conditions, were successfully cultured. These results suggest that storing contaminated water samples for 2 to 4 weeks in the dark at an ambient temperature prior to culturing can improve the isolation of Leptospira spp. from the samples. We implemented this protocol and collected water samples from natural sources accessed by both humans and animals. Leptospira spp. was identified in 32% (35/109) of water samples. The animal species using a water source influenced the likelihood of water samples being contaminated with Leptospira spp. Cultures of Leptospira spp. from environmental samples can provide useful information for understanding the complex interactions between humans, animals and the environment in the transmission of leptospirosis.en_US
dc.identifier.citationTropical Medicine and Infectious Disease. Vol.5, No.2 (2020)en_US
dc.identifier.doi10.3390/tropicalmed5020094en_US
dc.identifier.issn24146366en_US
dc.identifier.other2-s2.0-85087499931en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/57971
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087499931&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleOptimization of culture protocols to isolate Leptospira spp. From environmental water, field investigation, and identification of factors associated with the presence of Leptospira spp. From the environmenten_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85087499931&origin=inwarden_US

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