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Foreign Travel Is a Major Risk Factor for Colonization with Escherichia coliProducing CTX-M-Type Extended-Spectrum β-Lactamases: a Prospective Study with Swedish Volunteers
- Source :
- Antimicrobial Agents and Chemotherapy; September 2010, Vol. 54 Issue: 9 p3564-3568, 5p
- Publication Year :
- 2010
-
Abstract
- ABSTRACTForeign travel has been suggested to be a risk factor for the acquisition of extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae. To our knowledge, this has not previously been demonstrated in a prospective study. Healthy volunteers traveling outside Northern Europe were enrolled. Rectal swabs and data on potential travel-associated risk factors were collected before and after traveling. A total of 105 volunteers were enrolled. Four of them did not complete the study, and one participant carried ESBL-producing Escherichia colibefore travel. Twenty-four of 100 participants with negative pretravel samples were colonized with ESBL-producing Escherichia coliafter the trip. All strains produced CTX-M enzymes, mostly CTX-M-15, and some coproduced TEM or SHV enzymes. Coresistance to several antibiotic subclasses was common. Travel to India was associated with the highest risk for the acquisition of ESBLs (88%; n= 7). Gastroenteritis during the trip was an additional risk factor (P= 0.003). Five of 21 volunteers who completed the follow-up after 6 months had persistent colonization with ESBLs. This is the first prospective study demonstrating that international travel is a major risk factor for colonization with ESBL-producing Enterobacteriaceae. Considering the high acquisition rate of 24%, it is obvious that global efforts are needed to meet the emergence and spread of CTX-M enzymes and other antimicrobial resistances.
Details
- Language :
- English
- ISSN :
- 00664804 and 10986596
- Volume :
- 54
- Issue :
- 9
- Database :
- Supplemental Index
- Journal :
- Antimicrobial Agents and Chemotherapy
- Publication Type :
- Periodical
- Accession number :
- ejs57154380
- Full Text :
- https://doi.org/10.1128/AAC.00220-10