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DOI 10.1089/fpd.2019.2651

Медицинская библиотека · Foodborne pathogens and disease · 2019

Presence of OXA-48 Gene in a Clinical Isolate of Lactobacillus rhamnosus.

Hazırolan Gülşen, Gündoğdu Aycan, Nigiz Seyma, Altun Belgin, Gür Deniz

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Аннотация

Lactobacilli are part of the microbiota and are also used as probiotics. However, in recent years they have been associated with invasive infections, especially bacteremia. Lactobacillus spp. are usually susceptible to penicillins, macrolides, and carbapenems, but Lactobacillus rhamnosus is intrinsically resistant to glycopeptides. The aim of this study was to determine the antimicrobial susceptibility profile and resistance mechanism of a clinical isolate of L. rhamnosus isolated from 10 sets of blood cultures of the same patient. The isolate was identified by Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry (Bruker Daltonics; BD, Bremen, Germany) and 16S rRNA gene sequencing. In vitro susceptibilities to penicillin, ampicillin, imipenem, vancomycin, erythromycin, clindamycin, and linezolid were determined with gradient test strips (bioMérieux, France) on Mueller-Hinton agar plates supplemented with 5% defibrinated horse blood and 20 mg/L β-NAD. The isolate was resistant to vancomycin and imipenem. Polymerase chain reaction test was positive for blaOXA-48 and the presence of this carbapenemase was confirmed by gene sequencing. Although plasmid analysis suggested that the blaOXA-48 is chromosomal in this isolate, it is still an alarming finding for potential transmission of antibiotic resistance genes to other bacteria in the gut. To our knowledge, this is the first report of the presence of blaOXA-48 in a Lactobacillus spp. and has utmost importance as these bacteria are used as probiotics. The isolation of these bacteria from sterile body sites should not go unnoticed.

Для цитирования: Hazırolan Gülşen, Gündoğdu Aycan, Nigiz Seyma, Altun Belgin, Gür Deniz. Presence of OXA-48 Gene in a Clinical Isolate of Lactobacillus rhamnosus.. Foodborne pathogens and disease. 2019. DOI: 10.1089/fpd.2019.2651.

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