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Spread of multidrug resistance among Ureaplasma serovars, Tunisia

BACKGROUND: Ureaplasma spp. have been implicated in a variety of clinical conditions and certain serovars are likely to be disease-associated. Hence, the ascending trend of Ureaplasma spp. resistance to antimicrobials should deserve more attention. Here we assessed the extent of antimicrobial resist...

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Autores principales: Boujemaa, Safa, Mlik, Béhija, Ben Allaya, Amina, Mardassi, Helmi, Ben Abdelmoumen Mardassi, Boutheina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979072/
https://www.ncbi.nlm.nih.gov/pubmed/31998474
http://dx.doi.org/10.1186/s13756-020-0681-5
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author Boujemaa, Safa
Mlik, Béhija
Ben Allaya, Amina
Mardassi, Helmi
Ben Abdelmoumen Mardassi, Boutheina
author_facet Boujemaa, Safa
Mlik, Béhija
Ben Allaya, Amina
Mardassi, Helmi
Ben Abdelmoumen Mardassi, Boutheina
author_sort Boujemaa, Safa
collection PubMed
description BACKGROUND: Ureaplasma spp. have been implicated in a variety of clinical conditions and certain serovars are likely to be disease-associated. Hence, the ascending trend of Ureaplasma spp. resistance to antimicrobials should deserve more attention. Here we assessed the extent of antimicrobial resistance of Ureaplasma serovars in Tunisia, and investigated the underlying molecular basis. METHODS: This study included 101 molecularly typed Ureaplasma spp. clinical strains isolated over a 12-year time period (2005–2017). The antimicrobial susceptibility was tested against nine antibacterial agents using the broth microdilution method. Neighbor-joining tree was constructed to establish the phylogenetic relationships among isolates. RESULTS: We found that all ureaplasma isolates were resistant to ciprofloxacin and erythromycin, intermediately resistant to azithromycin, and susceptible to doxycycline, moxifloxacin and josamycin. Ofloxacin and levofloxacin resistance was found in 73.27 and 17.82%, respectively, while 37.62% of isolates proved resistant to tetracycline. Consequently, we detected an elevated multidrug resistance rate among ureaplasma isolates (37.62%), particularly among serovars 2, 5, 8, and 9 (77.77% overall), as well as serovars 4, 10, 12, and 13 (52.63% overall). In most cases, drug resistance was found to be associated with known molecular mechanisms, yet we have identified two novel mutations in the L22 protein, which might be associated with macrolide-resistance. CONCLUSION: To our knowledge, this is the first study that reports the widespread expansion of multidrug resistance among Ureaplasma serovars, a finding of importance in terms of both surveillance and antimicrobial usage.
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spelling pubmed-69790722020-01-29 Spread of multidrug resistance among Ureaplasma serovars, Tunisia Boujemaa, Safa Mlik, Béhija Ben Allaya, Amina Mardassi, Helmi Ben Abdelmoumen Mardassi, Boutheina Antimicrob Resist Infect Control Research BACKGROUND: Ureaplasma spp. have been implicated in a variety of clinical conditions and certain serovars are likely to be disease-associated. Hence, the ascending trend of Ureaplasma spp. resistance to antimicrobials should deserve more attention. Here we assessed the extent of antimicrobial resistance of Ureaplasma serovars in Tunisia, and investigated the underlying molecular basis. METHODS: This study included 101 molecularly typed Ureaplasma spp. clinical strains isolated over a 12-year time period (2005–2017). The antimicrobial susceptibility was tested against nine antibacterial agents using the broth microdilution method. Neighbor-joining tree was constructed to establish the phylogenetic relationships among isolates. RESULTS: We found that all ureaplasma isolates were resistant to ciprofloxacin and erythromycin, intermediately resistant to azithromycin, and susceptible to doxycycline, moxifloxacin and josamycin. Ofloxacin and levofloxacin resistance was found in 73.27 and 17.82%, respectively, while 37.62% of isolates proved resistant to tetracycline. Consequently, we detected an elevated multidrug resistance rate among ureaplasma isolates (37.62%), particularly among serovars 2, 5, 8, and 9 (77.77% overall), as well as serovars 4, 10, 12, and 13 (52.63% overall). In most cases, drug resistance was found to be associated with known molecular mechanisms, yet we have identified two novel mutations in the L22 protein, which might be associated with macrolide-resistance. CONCLUSION: To our knowledge, this is the first study that reports the widespread expansion of multidrug resistance among Ureaplasma serovars, a finding of importance in terms of both surveillance and antimicrobial usage. BioMed Central 2020-01-23 /pmc/articles/PMC6979072/ /pubmed/31998474 http://dx.doi.org/10.1186/s13756-020-0681-5 Text en © The Author(s). 2020 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
Boujemaa, Safa
Mlik, Béhija
Ben Allaya, Amina
Mardassi, Helmi
Ben Abdelmoumen Mardassi, Boutheina
Spread of multidrug resistance among Ureaplasma serovars, Tunisia
title Spread of multidrug resistance among Ureaplasma serovars, Tunisia
title_full Spread of multidrug resistance among Ureaplasma serovars, Tunisia
title_fullStr Spread of multidrug resistance among Ureaplasma serovars, Tunisia
title_full_unstemmed Spread of multidrug resistance among Ureaplasma serovars, Tunisia
title_short Spread of multidrug resistance among Ureaplasma serovars, Tunisia
title_sort spread of multidrug resistance among ureaplasma serovars, tunisia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6979072/
https://www.ncbi.nlm.nih.gov/pubmed/31998474
http://dx.doi.org/10.1186/s13756-020-0681-5
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