2016
DOI: 10.1128/aac.01576-16
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Prevalence of Quinolone Resistance in Enterobacteriaceae from Sierra Leone and the Detection of qnrB Pseudogenes and Modified LexA Binding Sites

Abstract: A collection of 74 Enterobacteriaceae isolates found in Bo, Sierra Leone, were tested for quinolone antibiotic susceptibility and resistance mechanisms. The majority of isolates (62%) were resistant to quinolones, and 61% harbored chromosomal gyrA and/or parC mutations. Plasmid-mediated quinolone resistance genes were ubiquitous, with qnrB and aac(6=)-Ib-cr being the most prevalent. Mutated LexA binding sites were found in all qnrB1 genes, and truncated qnrB pseudogenes were found in the majority of Citrobacte… Show more

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Cited by 8 publications
(8 citation statements)
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“…The qepA gene, one of the most recently identi ed PMQR determinants, has been associated with decreased susceptibility to uoroquinolones and increased MIC levels [24]. This determinant was detected in (16/188, 8.5%) E. coli isolates which was slightly lower compared to previous studies in Nigeria (18.5%) and Sierra Leon (23%) [27,29]. DNA sequencing con rmed the existence of the qepA gene among E. coli isolates in Kenya with F95L and V134I amino acid substitution consistent with amino acid substitution reported in the qepA4 allele [42].…”
Section: Discussionmentioning
confidence: 75%
“…The qepA gene, one of the most recently identi ed PMQR determinants, has been associated with decreased susceptibility to uoroquinolones and increased MIC levels [24]. This determinant was detected in (16/188, 8.5%) E. coli isolates which was slightly lower compared to previous studies in Nigeria (18.5%) and Sierra Leon (23%) [27,29]. DNA sequencing con rmed the existence of the qepA gene among E. coli isolates in Kenya with F95L and V134I amino acid substitution consistent with amino acid substitution reported in the qepA4 allele [42].…”
Section: Discussionmentioning
confidence: 75%
“…); the microarray used here does not provide this capability. Next generation sequencing can further provide high resolution epidemiological tracking and “One Health” linkages [ 95 , 96 ], provide context for genes, and even detect promoter modifications that significantly affect gene expression [ 97 , 98 ]. However, a key limitation of any molecular technology approach is that genotype may not always be predictive of phenotype if differential expression and/or functionality of expressed proteins is not known or fully characterized.…”
Section: Resultsmentioning
confidence: 99%
“…The low prevalence of the FQ resistance gene, qnrS , observed from all collection sites mirrored results from other studies [ 106 , 107 , 108 ]. This and other plasmid-mediated quinolone resistance (PMQR) genes reduce susceptibility to quinolones, albeit not always to the level of clinical resistance [ 98 , 109 ]. High-level resistance to first-line FQ therapeutics is generally conferred by point mutations in gyrA and parC in Enterobacteriaceae, which are not detectable by the microarray technology used here; the ability to interrogate samples for such point mutations would be an advantage of any sequencing-based approach.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, bla CMY -type, bla TEM -type, bla SHV -type, and bla DHA -type genes, in particular the latter three, were found to be encoded in one Citrobacter isolate and one Citrobacter plasmid for the first time, respectively. Quinolone resistance qnr genes and aminoglycoside resistance genes have been identified in Citrobacter species as well [68, 69], and the qnrB genes constitute the most predominant and variable group within the qnr family [70]. To the best of our knowledge, this work represents the first report of aadA16 in Citrobacter , as well as qnrB4 and aac6 in animal-associated C. freundii .…”
Section: Discussionmentioning
confidence: 97%