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Antimicrobial resistance acquisition after international travel in U.S. travelers

BACKGROUND: Prior studies have shown an increase in multidrug-resistant (MDR) E. coli colonization from two percent in U.S.-based to 11 % in deployed, healthy military personnel. It is unclear if colonization with MDR organisms occurs through deployment exposures or risks related to routine overseas...

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Autores principales: Blyth, Dana M., Mende, Katrin, Maranich, Ashley M., Beckius, Miriam L., Harnisch, Kristie A., Rosemann, Crystal A., Zera, Wendy C., Murray, Clinton K., Akers, Kevin S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531010/
https://www.ncbi.nlm.nih.gov/pubmed/28883948
http://dx.doi.org/10.1186/s40794-016-0020-2
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author Blyth, Dana M.
Mende, Katrin
Maranich, Ashley M.
Beckius, Miriam L.
Harnisch, Kristie A.
Rosemann, Crystal A.
Zera, Wendy C.
Murray, Clinton K.
Akers, Kevin S.
author_facet Blyth, Dana M.
Mende, Katrin
Maranich, Ashley M.
Beckius, Miriam L.
Harnisch, Kristie A.
Rosemann, Crystal A.
Zera, Wendy C.
Murray, Clinton K.
Akers, Kevin S.
author_sort Blyth, Dana M.
collection PubMed
description BACKGROUND: Prior studies have shown an increase in multidrug-resistant (MDR) E. coli colonization from two percent in U.S.-based to 11 % in deployed, healthy military personnel. It is unclear if colonization with MDR organisms occurs through deployment exposures or risks related to routine overseas travel. This study prospectively evaluates rates and risk factors associated with MDR gram-negative bacterial and methicillin-resistant S. aureus (MRSA) colonization after international travel. METHODS: Participants traveled internationally for five or more days. Pre- and post-travel, colonizing bacteria from oropharyngeal, nares, groin, and peri-rectal (PR) areas were collected using BD CultureSwab™ MaxV(+). Identification and susceptibilities were done utilizing the BD Phoenix™ Automated Microbiology System. Non-MDR pre- and post-travel MDR bacteria within a subject were compared by pulsed-field gel electrophoresis (PFGE). A questionnaire solicited demographics and potential risk factors for MDR acquisition. RESULTS: Of 58 participants, 41 % were male and median age was 64 years. Pre- and post-travel swabs were obtained a median of ten and seven days before and after travel, respectively. Itineraries included 18 participants traveling to the Caribbean and Central America, 17 to Asia, 16 to Africa, 5 to Europe, 4 to South and North America. Seventeen of 22 travelers used atovaquone/proguanil for malaria prophylaxis. The only MDR organism isolated was extended-spectrum β-lactamase (ESBL)-producing E. coli in five (9 %) participants post-travel (all PR and unrelated by PFGE). There were no statistically significant associations between exposure risks and new ESBL-producing E.coli colonization. Of 36 participants colonized with E. coli pre- and post-travel, new resistance was detected: TMP/SMX in 42 % of isolates (p < 0.01), tetracycline in 44 % (p < 0.01), and ampicillin-sulbactam in 33 % (p = 0.09). No participants were colonized with MRSA pre- or post-travel. CONCLUSION: Consistent with prior studies, new antimicrobial resistance was noted in colonizing E. coli after international travel. Nine percent of participants acquired new strains of ESBL-producing E.coli without identified risks.
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spelling pubmed-55310102017-09-07 Antimicrobial resistance acquisition after international travel in U.S. travelers Blyth, Dana M. Mende, Katrin Maranich, Ashley M. Beckius, Miriam L. Harnisch, Kristie A. Rosemann, Crystal A. Zera, Wendy C. Murray, Clinton K. Akers, Kevin S. Trop Dis Travel Med Vaccines Research BACKGROUND: Prior studies have shown an increase in multidrug-resistant (MDR) E. coli colonization from two percent in U.S.-based to 11 % in deployed, healthy military personnel. It is unclear if colonization with MDR organisms occurs through deployment exposures or risks related to routine overseas travel. This study prospectively evaluates rates and risk factors associated with MDR gram-negative bacterial and methicillin-resistant S. aureus (MRSA) colonization after international travel. METHODS: Participants traveled internationally for five or more days. Pre- and post-travel, colonizing bacteria from oropharyngeal, nares, groin, and peri-rectal (PR) areas were collected using BD CultureSwab™ MaxV(+). Identification and susceptibilities were done utilizing the BD Phoenix™ Automated Microbiology System. Non-MDR pre- and post-travel MDR bacteria within a subject were compared by pulsed-field gel electrophoresis (PFGE). A questionnaire solicited demographics and potential risk factors for MDR acquisition. RESULTS: Of 58 participants, 41 % were male and median age was 64 years. Pre- and post-travel swabs were obtained a median of ten and seven days before and after travel, respectively. Itineraries included 18 participants traveling to the Caribbean and Central America, 17 to Asia, 16 to Africa, 5 to Europe, 4 to South and North America. Seventeen of 22 travelers used atovaquone/proguanil for malaria prophylaxis. The only MDR organism isolated was extended-spectrum β-lactamase (ESBL)-producing E. coli in five (9 %) participants post-travel (all PR and unrelated by PFGE). There were no statistically significant associations between exposure risks and new ESBL-producing E.coli colonization. Of 36 participants colonized with E. coli pre- and post-travel, new resistance was detected: TMP/SMX in 42 % of isolates (p < 0.01), tetracycline in 44 % (p < 0.01), and ampicillin-sulbactam in 33 % (p = 0.09). No participants were colonized with MRSA pre- or post-travel. CONCLUSION: Consistent with prior studies, new antimicrobial resistance was noted in colonizing E. coli after international travel. Nine percent of participants acquired new strains of ESBL-producing E.coli without identified risks. BioMed Central 2016-03-14 /pmc/articles/PMC5531010/ /pubmed/28883948 http://dx.doi.org/10.1186/s40794-016-0020-2 Text en © Blyth et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Blyth, Dana M.
Mende, Katrin
Maranich, Ashley M.
Beckius, Miriam L.
Harnisch, Kristie A.
Rosemann, Crystal A.
Zera, Wendy C.
Murray, Clinton K.
Akers, Kevin S.
Antimicrobial resistance acquisition after international travel in U.S. travelers
title Antimicrobial resistance acquisition after international travel in U.S. travelers
title_full Antimicrobial resistance acquisition after international travel in U.S. travelers
title_fullStr Antimicrobial resistance acquisition after international travel in U.S. travelers
title_full_unstemmed Antimicrobial resistance acquisition after international travel in U.S. travelers
title_short Antimicrobial resistance acquisition after international travel in U.S. travelers
title_sort antimicrobial resistance acquisition after international travel in u.s. travelers
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531010/
https://www.ncbi.nlm.nih.gov/pubmed/28883948
http://dx.doi.org/10.1186/s40794-016-0020-2
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