在葡萄牙肺炎克雷伯菌临床分离株中,arr-2和arr-3的传播与1类整合子有关。

IF 5.5 3区 医学 Q1 IMMUNOLOGY
Rita Elias, Ana Modesto, Diana Machado, Bruna Pereira, Jody Phelan, José Melo-Cristino, Luís Lito, Luísa Gonçalves, Isabel Portugal, Miguel Viveiros, Susana Campino, Taane G Clark, Aida Duarte, João Perdigão
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引用次数: 0

摘要

肺炎克雷伯菌是卫生保健相关感染的常见病原体,表达大量抗微生物药物耐药性位点,包括能够介导利福平耐药性的adp -核糖基转移酶编码基因(arr)。后者通过抑制dna依赖的RNA聚合酶对多种微生物具有活性。本研究旨在描述138个临床分离的肺炎克雷伯菌arr分布和遗传背景,并将其与利福平耐药性联系起来。对所有分离株进行全基因组测序,进行物种鉴定、分型和AMR基因鉴定,并测定利福平的最低抑菌浓度(MIC)。对利福平耐药菌株进行arr基因和1类整合子的分子检测。外排活性被调查作为一个可能的决定因素,利福平耐药的分离缺乏已知的遗传决定因素。12株菌株具有高mic值(≥64 mg/L), 124株为中等mic值(16 ~ 32 mg/L), 2株为低mic值(8 mg/L)。两个arr等位基因变异,arr-2和arr-3,分别在1个和9个肺炎克雷伯菌分离株中被发现,它们都在1类整合子内,包括一个新描述的整合子,并且都与高利福平mic(≥64 mg/L)相关。抗性水平升高还与arr-2/3表达增加和与启动子更接近有关。在其余两个分离株中未发现arr基因或rpoB突变,并且在两个分离株中未发现外排活性与高水平利福平耐药性之间的相关性。总之,本研究表明,arr基因赋予肺炎克雷伯菌高水平的利福平耐药性,突出了其在1类整合子中的广泛传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dissemination of arr-2 and arr-3 is associated with class 1 integrons in Klebsiella pneumoniae clinical isolates from Portugal.

\nKlebsiella pneumoniae is a common pathogen of healthcare-associated infections expressing a plethora of antimicrobial resistance loci, including ADP-ribosyltransferase coding genes (arr), able to mediate rifampicin resistance. The latter has activity against a broad range of microorganisms by inhibiting DNA-dependent RNA polymerases. This study aims to characterise the arr distribution and genetic context in 138 clinical isolates of K. pneumoniae and correlate these with rifampicin resistance. All isolates were subjected to whole-genome sequencing for species identification, typing and AMR genes identification, along with the determination of the minimum inhibitory concentration (MIC) of rifampicin. Molecular detection of arr genes and class 1 integrons was performed for rifampicin-resistant isolates. Efflux activity was investigated as a possible determinant of rifampicin resistance in isolates devoid of known genetic determinants. Twelve isolates exhibited high rifampicin MICs (≥ 64 mg/L), 124 showed intermediate MICs (16-32 mg/L) and two displayed low (8 mg/L) MICs. Two arr allelic variants, arr-2 and arr-3, were found across one and nine K. pneumoniae isolates, respectively, all within class 1 integrons, including a newly described integron, and all associated with high rifampicin MICs  (≥ 64 mg/L). Elevated resistance levels were additionally linked to increased arr-2/3 expression and closer proximity to the promoter. No arr gene or rpoB mutations were found across the remaining two isolates and no correlation between efflux activity and high-level rifampicin resistance was found for both isolates. In conclusion, this study demonstrates that arr genes confer high levels of rifampicin resistance in K. pneumoniae highlighting its widespread dissemination within class 1 integrons.

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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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