Mutation-based fluoroquinolone resistance in carbapenem-resistant Acinetobacter baumannii and Escherichia coli isolates causing catheter-related bloodstream infections

被引:0
作者
Tawfick, Mahmoud M. [1 ,2 ]
Adulall, Abeer K. [3 ]
El-Kholy, Amani A. [4 ]
El Manakhly, Arwa Ramadan [5 ]
机构
[1] Al Azhar Univ, Fac Pharm Boys, Dept Microbiol & Immunol, Nasr City, Egypt
[2] Heliopolis Univ, Fac Pharm, Dept Microbiol & Immunol, Cairo, Egypt
[3] Al Azhar Univ, Fac Pharm Girls, Dept Microbiol & Immunol, Cairo, Egypt
[4] Cairo Univ, Fac Med, Dept Clin Pathol, Cairo, Egypt
[5] Modern Univ Technol & Informat MTI, Fac Pharm, Dept Microbiol & Immunol, 314 Yasmeen 6 St,First settlement, Cairo 11751, Egypt
来源
INTERNATIONAL JOURNAL OF HEALTH SCIENCES-IJHS | 2023年 / 17卷 / 03期
关键词
Acinetobacter baumannii; carbapenem resistance; catheter-related bloodstream infections; Escherichia coli; fluoroquinolone resistance; DESORPTION IONIZATION-TIME; FLIGHT MASS-SPECTROMETRY; INTENSIVE-CARE UNITS; ANTIMICROBIAL RESISTANCE; RISK-FACTORS; SUSCEPTIBILITY; MORTALITY; BACTERIA; MECHANISMS; HOSPITALS;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: We studied the presence of mutations in the chromosomal quinolone resistance-determining regions (QRDRs) of the fluoroquinolone targets gyrA and parC genes and detected the carbapenem resistance (CR) encoding genes among Acinetobacter baumannii and Escherichia coli isolates from catheter-related bloodstream infections (CRBSIs). Methods: The study included 39 non-duplicate isolates of A. baumannii (14/39, 35.9%) and E. coli (25/39, 64.1%) isolated from 128 confirmed CRBSIs cases. Antimicrobial susceptibility testing was performed, followed by an evaluation of biofilm formation using the tissue culture plate method. The carbapenemase encoding genes were detected by multiplex polymerase chain reaction (PCR). The mutations in QRDRs of gyrA and parC genes were determined by singleplex PCR amplification followed by DNA sequencing and BlastN analysis in the GenBank database. DNA and the translated amino acid sequences were analyzed using the Mega7 bioinformatics tool. Results: Multidrug-resistant (MDR) E. coli and A. baumannii isolates harbored CR encoding genes and combined gyrA and parC genes mutation. The specific substitutions observed in GyrA were Cys173Arg, Cys174Gly, Asp80Val, Tyr178ASP, Tyr84Gly, Glu85Lys, Ser172Leu, and Asp176Asn, while the specific substitutions observed in the ParC amino acid sequence were point mutation 62 Arg, Phe60Leu, Ils66Val, and Gln76Lys. Point mutation 62Arg was detected in two A. baumannii isolates, whereas Ser172Leu mutation was observed in two E. coli isolates. Conclusion: The presence of new single and multiple mutations in QRDR causes the emergence of MDR E. coli and A. baumannii infections in carbapenem-resistant Enterobacteriaceae in Egypt, requiring further investigation in Gram-negative bacteria.
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页码:18 / 25
页数:8
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