Literature DB >> 12705683

Antimicrobial resistance in recent fecal enterococci from healthy volunteers and food handlers in Spain: genes and phenotypes.

R del Campo1, P Ruiz-Garbajosa, M P Sánchez-Moreno, F Baquero, C Torres, R Cantón, T M Coque.   

Abstract

Susceptibility patterns to 15 different antibiotics and the presence of resistance genes were evaluated in recent fecal Enterococcus isolates recovered from 42 healthy volunteers (HV) and 43 food-handlers (FH). A total of 142 Enterococcus faecalis, 74 Enterococcus faecium, and 23 Enterococcus spp. with different antibiotic susceptibility patterns were studied. A higher percentage of resistance for moxifloxacin, erythromycin, glycopeptides and high-level resistance (HLR) to gentamicin were observed in the FH group. Ampicillin- or linezolid-resistant isolates were not recovered in any of the groups. The tet(M) gene was found in 96% and in 85% of tetracycline-resistant isolates from HV and FH, respectively. HLR-kanamycin was mediated by aph(3')-IIIa, or aac(6')-aph(2"), or both genes in all isolates from HV group and in 86% from FH group. The aac(6')-aph(2") gene was found in all HLR-gentamicin isolates. Ninety-one percent of HV and 71% of FH erythromycin-resistant isolates harbored the erm(B) gene (erythromycin MIC range of 8-128 microg/ml), whereas erm(A), erm(C), or mef(A) genes were not detected. Coexistence of erm(B), aph(3')-IIIa, and tet(M) genes was observed in 17% of the isolates of both groups. The HLR-gentamicin isolates presented unrelated PFGE patterns while 2 out of 3 vanA E. faecium isolates showed an indistinguishable SmaI-pulsed-field gel electrophoresis (PFGE) pattern. This study shows that despite 4 years of official banning of antibiotic growth promoters in animals, enterococci isolated from FH are more resistant than those from HV. This suggests the permanence of resistant clones or transferable resistance elements in farms and a possible exchange between food products and humans, or eventually the long-term permanence of certain clones in the FH intestinal tract.

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Year:  2003        PMID: 12705683     DOI: 10.1089/107662903764736346

Source DB:  PubMed          Journal:  Microb Drug Resist        ISSN: 1076-6294            Impact factor:   3.431


  5 in total

1.  Multilocus sequence typing scheme for Enterococcus faecalis reveals hospital-adapted genetic complexes in a background of high rates of recombination.

Authors:  Patricia Ruiz-Garbajosa; Marc J M Bonten; D Ashley Robinson; Janetta Top; Sreedhar R Nallapareddy; Carmen Torres; Teresa M Coque; Rafael Cantón; Fernando Baquero; Barbara E Murray; Rosa del Campo; Rob J L Willems
Journal:  J Clin Microbiol       Date:  2006-06       Impact factor: 5.948

2.  Dogs are a reservoir of ampicillin-resistant Enterococcus faecium lineages associated with human infections.

Authors:  Peter Damborg; Janetta Top; Antoni P A Hendrickx; Susan Dawson; Rob J L Willems; Luca Guardabassi
Journal:  Appl Environ Microbiol       Date:  2009-02-20       Impact factor: 4.792

3.  Phylogeny, Biofilm Production, and Antimicrobial Properties of Fecal Microbial Communities of Adi Tribes of Arunachal Pradesh, India.

Authors:  Parijat Hazarika; Indranil Chattopadhyay; Mika Umpo; Yashmin Choudhury; Indu Sharma
Journal:  Appl Biochem Biotechnol       Date:  2021-03-03       Impact factor: 2.926

4.  Genetic relatedness of the Enterococcus faecalis isolates in stool and urine samples of patients with community-acquired urinary tract infection.

Authors:  Zohreh Ghalavand; Masoud Alebouyeh; Kiandokht Ghanati; Leila Azimi; Marjan Rashidan
Journal:  Gut Pathog       Date:  2020-09-09       Impact factor: 4.181

5.  Evaluating Food Safety Compliance and Hygiene Practices of Food Handlers Working in Community and Healthcare Settings in Kuwait.

Authors:  Ola H Moghnia; Vincent O Rotimi; Noura A Al-Sweih
Journal:  Int J Environ Res Public Health       Date:  2021-02-08       Impact factor: 3.390

  5 in total

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