Antibiotic resistance genes in phage particles isolated from human faeces and induced from clinical bacterial isolates


Por: Brown-Jaque, M, Calero-Caceres, W, Espinal, P, Rodriguez-Navarro, J, Miro, E, Gonzalez-Lopez, JJ, Cornejo, T, Hurtado, JC, Navarro, F, Muniesa, M

Publicada: 1 mar 2018
Resumen:
Phage particles have emerged as elements with the potential to mobilise antibiotic resistance genes (ARGs) in different environments, including the intestinal habitat. This study aimed to determine the occurrence of ARGs in phage particles present in faecal matter and induced from strains isolated from faeces. Nine ARGs (bla(TEM), bla(CTX-M-1 group), bla(CTX-M-9 group), bla(OXA-48), qnrA, qnrS, mecA, sul1 and armA) were quantified by qPCR in the phage DNA fractions of 150 faecal samples obtained from healthy individuals who had not received antibiotic treatment or travelled abroad in the 3 months prior to sample collection. On the suspicion that the detected particles originated from bacterial flora, 82 Escherichia coli and Klebsiella pneumoniae isolates possessing at least one identified ARG (bla(TEM), bla(CTX-M-1 group), bla(CTX-M-9 group), armA, qnrA, qnrS and sul1) were isolated and their capacity to produce phage particles carrying these ARGs following induction was evaluated. Of 150 samples, 72.7% were positive for at least one ARG, with bla(TEM) and bla(CTX-M-9 group) being the most prevalent and abundant. Of the 82 isolates, 51 (62%) showed an increase in the number of copies of the respective ARG in the phage fraction following induction, with bla(TEM), bla(CTX-M-1 group), bla(CTX-M-9 group) and sul1 being the most abundant. Phages induced from the isolates were further purified and visualised using microscopy and their DNA showed ARG levels of up to 1010 gene copies/mL. This study highlights the abundance of phage particles harbouring ARGs and indicates that bacterial strains in the intestinal habitat could be source of these particles. (C) 2017 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.

Filiaciones:
Brown-Jaque, M:
 Univ Barcelona, Dept Genet Microbiol & Stat, Diagonal 643,Floor 0, E-08028 Barcelona, Spain

Calero-Caceres, W:
 Univ Barcelona, Dept Genet Microbiol & Stat, Diagonal 643,Floor 0, E-08028 Barcelona, Spain

Espinal, P:
 Hosp Santa Creu & Sant Pau, Serv Microbiol, Inst Invest Biomed St Pau, Sant Quinti 89, Barcelona 08041, Spain

Rodriguez-Navarro, J:
 Hosp Santa Creu & Sant Pau, Serv Microbiol, Inst Invest Biomed St Pau, Sant Quinti 89, Barcelona 08041, Spain

 Univ Autonoma Barcelona, Dept Genet & Microbiol, Barcelona, Spain

Miro, E:
 Hosp Santa Creu & Sant Pau, Serv Microbiol, Inst Invest Biomed St Pau, Sant Quinti 89, Barcelona 08041, Spain

Gonzalez-Lopez, JJ:
 Hosp Valle De Hebron, Vall dHebron Inst Recerca, Dept Clin Microbiol, Barcelona, Spain

Cornejo, T:
 Hosp Valle De Hebron, Vall dHebron Inst Recerca, Dept Clin Microbiol, Barcelona, Spain

Hurtado, JC:
 Univ Barcelona, Hosp Clin Barcelona, Barcelona Ctr Int Hlth Res, ISGlobal,Dept Microbiol, Barcelona, Spain

Navarro, F:
 Hosp Santa Creu & Sant Pau, Serv Microbiol, Inst Invest Biomed St Pau, Sant Quinti 89, Barcelona 08041, Spain

 Univ Autonoma Barcelona, Dept Genet & Microbiol, Barcelona, Spain

Muniesa, M:
 Univ Barcelona, Dept Genet Microbiol & Stat, Diagonal 643,Floor 0, E-08028 Barcelona, Spain
ISSN: 09248579
Editorial
ELSEVIER, RADARWEG 29, 1043 NX AMSTERDAM, NETHERLANDS, Países Bajos
Tipo de documento: Article
Volumen: 51 Número: 3
Páginas: 434-442
WOS Id: 000427582000021
ID de PubMed: 29180282
imagen Green Accepted

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