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A Cost-Effective Method for Identifying Enterobacterales with OXA-181.


ABSTRACT: OXA-181 is the second most common global OXA-48-like carbapenemase and is endemic in the Indian subcontinent. Molecular studies have shown that Enterobacterales with OXA-181 are often introduced into regions of nonendemicity. Distinguishing OXA-181 from other OXA-48-like enzymes often requires sequencing, which is rather expensive and time-consuming. A specific PCR (i.e., OXA181PCR) for the detection of bla OXA-181 was validated using a global collection (n?=?315) of bacteria with well-characterized carbapenemases and showed 100% sensitivity and specificity (95% confidence interval [CI], 94.1 to 100 and 98.6 to 100, respectively) for detecting bacteria with OXA-181. The OXA181PCR subsequently gave positive results on 58/160 (36%) Enterobacterales with OXA-48-like carbapenemases from the 2015 INFORM surveillance program. The bla OXA-181-positive Enterobacterales were present in 9 countries spanning 5 continents, illustrating the global distribution of OXA-181. This methodology can easily be incorporated into molecular surveillance programs to provide accurate information about the prevalence of OXA-181. A loop-mediated isothermal amplification (LAMP)-OXA48 assay overall performed well for detecting OXA-48-like enzymes but showed poor specificity due to false-positive results with non-OXA carbapenemases.

SUBMITTER: Peirano G 

PROVIDER: S-EPMC6813009 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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A Cost-Effective Method for Identifying <i>Enterobacterales</i> with OXA-181.

Peirano Gisele G   Matsumura Yasufumi Y   Nobrega Diego D   Pitout Johann D D JDD  

Journal of clinical microbiology 20191023 11


OXA-181 is the second most common global OXA-48-like carbapenemase and is endemic in the Indian subcontinent. Molecular studies have shown that <i>Enterobacterales</i> with OXA-181 are often introduced into regions of nonendemicity. Distinguishing OXA-181 from other OXA-48-like enzymes often requires sequencing, which is rather expensive and time-consuming. A specific PCR (i.e., OXA181PCR) for the detection of <i>bla</i><sub>OXA-181</sub> was validated using a global collection (<i>n</i> = 315)  ...[more]

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