Multiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients
Abstract Fluoroquinolones have been used for prophylaxis against infections in cancer patients but their impact on the resistance mechanisms still require further investigation. To elucidate mechanisms underlying ciprofloxacin (CIP) resistance in Gram-negative pathogens causing infections to cancer...
Guardado en:
Autores principales: | , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/0d34a39e48fa4b6a9a9ac10e7aa954d6 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:0d34a39e48fa4b6a9a9ac10e7aa954d6 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:0d34a39e48fa4b6a9a9ac10e7aa954d62021-12-02T15:07:49ZMultiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients10.1038/s41598-018-30756-42045-2322https://doaj.org/article/0d34a39e48fa4b6a9a9ac10e7aa954d62018-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-30756-4https://doaj.org/toc/2045-2322Abstract Fluoroquinolones have been used for prophylaxis against infections in cancer patients but their impact on the resistance mechanisms still require further investigation. To elucidate mechanisms underlying ciprofloxacin (CIP) resistance in Gram-negative pathogens causing infections to cancer patients, 169 isolates were investigated. Broth microdilution assays showed high-level CIP resistance in 89.3% of the isolates. Target site mutations were analyzed using PCR and DNA sequencing in 15 selected isolates. Of them, all had gyrA mutations (codons 83 and 87) with parC mutations (codons 80 and 84) in 93.3%. All isolates were screened for plasmid-mediated quinolone resistance (PMQR) genes and 56.8% of them were positive in this respect. Among PMQR genes, aac(6′)-Ib-cr predominated (42.6%) while qnr genes were harbored by 32.5%. This comprised qnrS in 26.6% and qnrB in 6.5%. Clonality of the qnr-positive isolates using ERIC-PCR revealed that most of them were not clonal. CIP MIC reduction by CCCP, an efflux pump inhibitor, was studied and the results revealed that contribution of efflux activity was observed in 18.3% of the isolates. Furthermore, most fluoroquinolone resistance mechanisms were detected among Gram-negative isolates recovered from cancer patients. Target site mutations had the highest impact on CIP resistance as compared to PMQRs and efflux activity.Samira M. HamedWalid F. ElkhatibHadir A. El-MahallawyMai M. HelmyMohamed S. AshourKhaled M. A. AboshanabNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-10 (2018) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Samira M. Hamed Walid F. Elkhatib Hadir A. El-Mahallawy Mai M. Helmy Mohamed S. Ashour Khaled M. A. Aboshanab Multiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients |
description |
Abstract Fluoroquinolones have been used for prophylaxis against infections in cancer patients but their impact on the resistance mechanisms still require further investigation. To elucidate mechanisms underlying ciprofloxacin (CIP) resistance in Gram-negative pathogens causing infections to cancer patients, 169 isolates were investigated. Broth microdilution assays showed high-level CIP resistance in 89.3% of the isolates. Target site mutations were analyzed using PCR and DNA sequencing in 15 selected isolates. Of them, all had gyrA mutations (codons 83 and 87) with parC mutations (codons 80 and 84) in 93.3%. All isolates were screened for plasmid-mediated quinolone resistance (PMQR) genes and 56.8% of them were positive in this respect. Among PMQR genes, aac(6′)-Ib-cr predominated (42.6%) while qnr genes were harbored by 32.5%. This comprised qnrS in 26.6% and qnrB in 6.5%. Clonality of the qnr-positive isolates using ERIC-PCR revealed that most of them were not clonal. CIP MIC reduction by CCCP, an efflux pump inhibitor, was studied and the results revealed that contribution of efflux activity was observed in 18.3% of the isolates. Furthermore, most fluoroquinolone resistance mechanisms were detected among Gram-negative isolates recovered from cancer patients. Target site mutations had the highest impact on CIP resistance as compared to PMQRs and efflux activity. |
format |
article |
author |
Samira M. Hamed Walid F. Elkhatib Hadir A. El-Mahallawy Mai M. Helmy Mohamed S. Ashour Khaled M. A. Aboshanab |
author_facet |
Samira M. Hamed Walid F. Elkhatib Hadir A. El-Mahallawy Mai M. Helmy Mohamed S. Ashour Khaled M. A. Aboshanab |
author_sort |
Samira M. Hamed |
title |
Multiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients |
title_short |
Multiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients |
title_full |
Multiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients |
title_fullStr |
Multiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients |
title_full_unstemmed |
Multiple mechanisms contributing to ciprofloxacin resistance among Gram negative bacteria causing infections to cancer patients |
title_sort |
multiple mechanisms contributing to ciprofloxacin resistance among gram negative bacteria causing infections to cancer patients |
publisher |
Nature Portfolio |
publishDate |
2018 |
url |
https://doaj.org/article/0d34a39e48fa4b6a9a9ac10e7aa954d6 |
work_keys_str_mv |
AT samiramhamed multiplemechanismscontributingtociprofloxacinresistanceamonggramnegativebacteriacausinginfectionstocancerpatients AT walidfelkhatib multiplemechanismscontributingtociprofloxacinresistanceamonggramnegativebacteriacausinginfectionstocancerpatients AT hadiraelmahallawy multiplemechanismscontributingtociprofloxacinresistanceamonggramnegativebacteriacausinginfectionstocancerpatients AT maimhelmy multiplemechanismscontributingtociprofloxacinresistanceamonggramnegativebacteriacausinginfectionstocancerpatients AT mohamedsashour multiplemechanismscontributingtociprofloxacinresistanceamonggramnegativebacteriacausinginfectionstocancerpatients AT khaledmaaboshanab multiplemechanismscontributingtociprofloxacinresistanceamonggramnegativebacteriacausinginfectionstocancerpatients |
_version_ |
1718388365387104256 |