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DOI 10.3389/fmicb.2016.01671

Медицинская библиотека · Frontiers in microbiology · 2016

Antimicrobial Susceptibility of Autochthonous Aquatic Vibrio cholerae in Haiti.

Baron Sandrine, Lesne Jean, Jouy Eric, Larvor Emeline, Kempf Isabelle, Boncy Jacques, Rebaudet Stanilas, Piarroux Renaud

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Аннотация

We investigated the antimicrobial susceptibility of 50 environmental isolates of Vibrio cholerae non-O1/non-O139 collected in surface waters in Haiti in July 2012, during an active cholera outbreak. A panel of 16 antibiotics was tested on the isolates using the disk diffusion method and PCR detection of seven resistance-associated genes (strA/B, sul1/2, ermA/B, and mefA). All isolates were susceptible to amoxicillin-clavulanic acid, cefotaxime, imipenem, ciprofloxacin, norfloxacin, amikacin, and gentamicin. Nearly a quarter (22.0%) of the isolates were susceptible to all 16 antimicrobials tested and only 8.0% of the isolates (n = 4) were multidrug-resistant. The highest proportions of resistant isolates were observed for sulfonamide (70.0%), amoxicillin (12.0%), and trimethoprim-sulfamethoxazole (10.0%). One strain was resistant to erythromycin and one to doxycycline, two antibiotics used to treat cholera in Haiti. Among the 50 isolates, 78% possessed at least two resistance-associated genes, and the genes sul1, ermA, and strB were detected in all four multidrug-resistant isolates. Our results clearly indicate that the autochthonous population of V. cholerae non-O1/non-O139 found in surface waters in Haiti shows antimicrobial patterns different from that of the outbreak strain. The presence in the Haitian aquatic environment of V. cholerae non-O1/non-O139 with reduced susceptibility or resistance to antibiotics used in human medicine may constitute a mild public health threat.

Для цитирования: Baron Sandrine, Lesne Jean, Jouy Eric, Larvor Emeline, Kempf Isabelle, Boncy Jacques, Rebaudet Stanilas, Piarroux Renaud. Antimicrobial Susceptibility of Autochthonous Aquatic Vibrio cholerae in Haiti.. Frontiers in microbiology. 2016. DOI: 10.3389/fmicb.2016.01671.
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