Evidence map›Paper›PMID 39143645›Full record

ArticleEuropean journal of medical research2024

Prevalence of plasmid-mediated quinolone resistance genes and biofilm formation in different species of quinolone-resistant clinical Shigella isolates: a cross-sectional study.

Noor S K Al-Khafaji, Batool Shakir Abed Almjalawi, Ruqaya Munther J Ewadh, Hussein O M Al-Dahmoshi, Suhad Y Abed, Ava Nasrolahi, David Chinemerem Nwobodo, Manal Hadi Ghaffoori Kanaan, Sura Saad Abdullah, Morteza Saki

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Article in European journal of medical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Noor S K Al-KhafajiDepartment of Biology, College of Science, University of Babylon, Hilla, Iraq.
Batool Shakir Abed AlmjalawiGeneral Directorate of Education in Kerbala, Kerbala, Iraq.
Ruqaya Munther J EwadhCollege of Pharmacy, University of Babylon, Hilla, Iraq.
Hussein O M Al-DahmoshiDepartment of Biology, College of Science, University of Babylon, Hilla, Iraq.
Suhad Y AbedDepartment of Biology, College of Science, Mustansiriyah University, Baghdad, Iraq.
Ava NasrolahiInfectious Ophthalmologic Research Center, Imam Khomeini Hospital Clinical Research Development Unit, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
David Chinemerem NwobodoDepartment of Microbiology, Renaissance University, Enugu, Nigeria.
Manal Hadi Ghaffoori KanaanDepartment of Nursing, Technical Institute of Suwaria, Middle Technical University, Baghdad, Iraq.
Sura Saad AbdullahCollege of Pharmacy, Ajou University, Suwon, 16499, Republic of Korea.
Morteza SakiInfectious Ophthalmologic Research Center, Imam Khomeini Hospital Clinical Research Development Unit, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. mortezasaki1981@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe purpose of this study was to look into the presence of plasmid-mediated quinolone resistance (PMQR) genes and biofilm formation in several species of clinical Shigella isolates that were resistant to quinolones.

methodsThe stool samples of 150 patients (younger than 10 years) with diarrhea were collected in this cross-sectional study (November 2020 to December 2021). After cultivation of samples on Hektoen Enteric agar and xylose lysine deoxycholate agar, standard microbiology tests, VITEK 2 system, and polymerase chain reaction (PCR) were utilized to identify Shigella isolates. The broth microdilution method was used to determine antibiotic susceptibility. PMQR genes including qnrA, qnrB, qnrC, qnrD, qnrE, qnrS, qnrVC, qepA, oqxAB, aac(6')-Ib-cr, and crpP and biofilm formation were investigated in quinolone-resistant isolates by PCR and microtiter plate method, respectively. An enterobacterial repetitive intergenic consensus polymerase chain reaction (ERIC-PCR) technique was used to determine the clonal relatedness of quinolone-resistant isolates.

resultsA total of 95 Shigella isolates including S. sonnei (53, 55.8%), S. flexneri (39, 41.1%), and S. boydii (3, 3.2%) were identified. The highest resistance rates of the isolates were against ampicillin (92.6%, n = 88/95). Overall, 42 of 95 (44.2%) isolates were simultaneously resistant against two or more quinolones including 26 (61.9%) S. sonnei and 16 (38.1%) S. flexneri. All isolates were multidrug-resistant (resistance to more than 3 antibiotics). The occurrence of PMQR genes was as follows: qnrS (52.4%), qnrA and aac(6')-Ib-cr (33.3%), and qnrB (19.0%). The prevalence in species was as follows: 61.5% and 37.5% (qnrS), 19.2% and 56.3% (qnrA), 38.5% and 25.0 (aac(6')-Ib-cr), and 19.2% and 18.8% (qnrB) for S. sonnei and S. flexneri, respectively. The other PMQR genes were not detected. In total, 52.8% (28/53) of quinolone-susceptible and 64.3% (27/42) of quinolone-resistant isolates were biofilm producers. Biofilm formation was not significantly different between quinolone-resistant and quinolone-susceptible isolates (P-value = 0.299). Quinolone-resistant isolates showed a high genetic diversity according to the ERIC-PCR.

conclusionIt seems that qnrS, qnrA, and aac(6')-Ib-cr play a significant role in the quinolone resistance among Shigella isolates in our region. Also the quinolone-resistant S. flexneri and S. sonnei isolates had a high genetic diversity. Hence, antibiotic therapy needs to be routinely revised based on the surveillance findings.

Indexed as

Anti-Bacterial AgentsBiofilmsMicrobial Sensitivity TestsPlasmidsQuinolonesShigellaCross-Sectional StudiesDrug Resistance, BacterialDysentery, BacillaryFemaleHumansPrevalenceAnti-Bacterial AgentsQuinolonesERIC-PCRIraqPMQRQuinolone resistanceShigella

Identifiers

PMID39143645
PMCPMC11323402

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.