Last data update: Sep 23, 2024. (Total: 47723 publications since 2009)
Records 1-2 (of 2 Records) |
Query Trace: Travis TC [original query] |
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Survey of Legionella species found in Thai soil
Travis TC , Brown EW , Peruski LF , Siludjai D , Jorakate P , Salika P , Yang G , Kozak NA , Kodani M , Warner AK , Lucas CE , Thurman KA , Winchell JM , Thamthitiwat S , Fields BS . Int J Microbiol 2012 2012 218791 Members of the Gram-negative genus Legionella are typically found in freshwater environments, with the exception of L. longbeachae, which is present in composts and potting mixes. When contaminated aerosols are inhaled, legionellosis may result, typically as either the more serious pneumonia Legionnaires' disease or the less severe flu-like illness Pontiac fever. It is presumed that all species of the genus Legionella are capable of causing disease in humans. As a followup to a prior clinical study of legionellosis in rural Thailand, indigenous soil samples were collected proximal to cases' homes and workplaces and tested for the presence of legionellae by culture. We obtained 115 isolates from 22/39 soil samples and used sequence-based methods to identify 12 known species of Legionella represented by 87 isolates. |
Application of TaqMan low-density arrays for simultaneous detection of multiple respiratory pathogens.
Kodani M , Yang G , Conklin LM , Travis TC , Whitney CG , Anderson LJ , Schrag SJ , Taylor TH Jr , Beall BW , Breiman RF , Feikin DR , Njenga MK , Mayer LW , Oberste MS , Tondella ML , Winchell J , Lindstrom S , Erdman DD , Fields BS . J Clin Microbiol 2011 49 (6) 2175-82 The large and growing number of viral and bacterial pathogens responsible for respiratory infections poses a challenge for laboratories to provide rapid and comprehensive pathogen identification. We evaluated a novel application of the TaqMan(R) Low Density Array (TLDA) cards for real-time PCR detection of 21 respiratory pathogen targets. TLDA performance was compared to individual real-time PCR (IRTP) assays with the same primers and probes using 1) nucleic acids extracted from the 21 pathogen strains and 66 closely-related viruses and bacteria and 2) 292 clinical respiratory specimens. Using spiked samples, TLDA cards were about ten-fold less sensitive than the IRTP assays. Using 292 clinical specimens to generate 2238 paired individual assays, TLDA exhibited 89% sensitivity (95% confidence interval [CI] 86-92; 47-100 range per target) and 98% specificity (95% CI 97-99; 85-100 range per target) overall compared to IRTP real-time assays as the gold standard with a Ct cut-off of 43. The TLDA card approach offers promise for rapid and simultaneous identification of multiple respiratory pathogens for outbreak investigations and disease surveillance. |
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