基于全基因组测序鉴定和确定坦桑尼亚地区转诊医院患者分离的耐甲氧西林和甲氧西林敏感金黄色葡萄球菌对喹诺酮类药物的耐药性。

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Masoud A Juma, Happiness Kumburu, Boaz Wadugu, Davis Kuchaka, Mariana Shayo, Patrick Kimu, Livin E Kanje, Melkiory Beti, Marco van Zwetselaar, Blandina Mmbaga, Tolbert Sonda
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引用次数: 0

摘要

背景:耐甲氧西林金黄色葡萄球菌(MRSA)耐药基因 mecA 的出现给治疗和控制相关感染带来了巨大挑战。尽管喹诺酮类药物历来对 MRSA 和甲氧西林易感金黄色葡萄球菌(MSSA)菌株均有效,但金黄色葡萄球菌分离株(尤其是 MRSA)对喹诺酮类药物的耐药性不断上升,严重削弱了喹诺酮类药物的效力,进一步缩小了治疗选择范围。本研究旨在通过构建系统发育树,确定MRSA在分离菌株中的负担,以及它们的耐药性概况、基因型特征和分子亲缘关系:对来自坦桑尼亚大陆多多马、松盖亚、基戈马、基特特和莫罗戈罗以及桑给巴尔的姆纳齐-姆莫亚的六家地区转诊医院的临床金黄色葡萄球菌分离株进行了分析。细菌鉴定采用传统微生物学方法和 Illumina Nextseq 550 测序仪进行全基因组测序。物种鉴定使用 KmerFinder 3.2,多焦点序列分型使用 MLST 2.0,SCCmec 分型使用 SCCmecFinder 1.2,抗性基因使用 ResFinder 4.1,系统发育相关性使用 CSI Phylogeny 1.4:在分析的 140 个分离株中,69 个(49.3%)被鉴定为 MRSA,其中 57 个(82.6%)对喹诺酮类药物具有耐药性。相反,有 71 个分离物被鉴定为 MSSA,其中没有一个对奎诺酮类药物产生耐药性。孢子类型鉴定显示了六种孢子类型,其中以 t355、t1476 和 t498 型最为常见。此外,所有(69 个)MRSA 都携带 SCCmec IV 型。这些分离物表现出 14 种不同的序列类型(ST)。值得注意的是,ST152 在 MSSA(50 个分离株,70%)中很普遍,而 ST8 是 MRSA 的主要序列类型(58 个分离株,84%)。抗菌药耐药性图谱显示至少有三种水平获得的耐药基因,其中 blaZ、dfrG、tet(K)和 aac(6')-aph(2'')基因非常普遍:结论:坦桑尼亚地区医院中的金黄色葡萄球菌分离株具有高度的遗传多样性,MRSA分离株对喹诺酮类药物的耐药性令人担忧。MRSA菌系间耐药基因的多样性强调了发展可持续的抗菌药物管理和监测的必要性,以支持在社区和医院环境中管理和控制MRSA感染的循证指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Whole genome sequencing-based characterization and determination of quinolone resistance among methicillin-resistant and methicillin-susceptible S. Aureus isolates from patients attending regional referral hospitals in Tanzania.

Background: The emergence of multidrug-resistant termed Methicillin-resistant Staphylococcus aureus (MRSA) strain, driven by the acquisition of resistance gene mecA imposes a substantial challenge in the treatment and control of their related infections. Although quinolones have historically been effective against both MRSA and methicillin-susceptible S. aureus (MSSA) strains, the rising resistance to quinolones among S. aureus isolates, particularly in MRSA, has severely curtailed their potency and further narrowed down the therapeutic options. This study aimed to determine the burden of MRSA among isolates, as well as their resistance profile, genotypic characterization, and molecular relatedness through the construction of a phylogenetic tree.

Materials and methods: Archived clinical S. aureus isolates from a descriptive, cross-sectional study involving six regional referral hospitals in Dodoma, Songea, Kigoma, Kitete, and Morogoro in the mainland Tanzania and Mnazi Mmoja in Zanzibar were analyzed. Bacterial identification was performed using both classical microbiology and whole genome sequencing on Illumina Nextseq 550 Sequencer. Species identification was done using KmerFinder 3.2, Multilocus Sequence Typing using MLST 2.0, SCCmec typing using SCCmecFinder 1.2, resistance genes using ResFinder 4.1, and phylogenetic relatedness using CSI Phylogeny 1.4.

Results: Out of the 140 isolates analyzed, 69 (49.3%) were identified as MRSA, with 57 (82.6%) exhibiting quinolone resistance. Conversely, 71 isolates were identified as MSSA, and none of them exhibited resistance to quinolones. Spa-typing revealed six spa types, with t355, t1476, and t498 being the most common. Moreover, all (69) MRSA were found to carry SCCmec type IV. The isolates exhibited 14 different sequence types (STs). Notably, ST152 was prevalent among MSSA (50 isolates, 70%), while ST8 was the predominant sequence type among MRSA (58 isolates, 84%). The antimicrobial resistance profile revealed at least three horizontally acquired resistance genes, with blaZ, dfrG, tet(K), and aac (6')-aph (2'') genes being highly prevalent.

Conclusion: There is a high genetic diversity among the S. aureus isolates existing in Tanzania regional hospitals, with a concerning burden of quinolone resistance among MRSA isolates. The diversity in resistance genes among MRSA lineages emphasizes the necessity for the development of sustainable antimicrobial stewardship and surveillance to support evidence-based guidelines for managing and controlling MRSA infections in both community and hospital settings.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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