一种儿科病原体的进化适应:新出现的鼠伤寒沙门氏菌单相变异的低炎症和高抗性表型1,4,bb0,12: 1。

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Tengfei Shi, Huahong Qiu, Shaohan Xu, Hui Zhong, Huifang Huang, Huiyu Chen
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引用次数: 0

摘要

肠沙门氏菌血清型1,4,bb1,1,12:i:- (S.1,4,[5],12:i:-)是鼠伤寒沙门氏菌(S. typhimurium)的一种单相变异,是一种新兴的多重耐药病原体,对儿童健康构成重大威胁。对该变异的研究仍然有限,并且由于传统鉴定方法的挑战,S.1,4,[5],12:i:-经常被错误地归类为鼠伤寒沙门氏菌。本研究收集了2014年至2023年福建省122例S.1,4,[5],12:i:-和42例传统鼠伤寒沙门氏菌感染的临床数据。菌株分析采用全基因组测序。结果表明,77.87%的s1、4、bb0、12i -感染患儿年龄在1个月至2岁之间。与传统鼠伤寒沙门氏菌相比,S.1,4,[5],12:i:-患儿临床症状较轻,炎症标志物c反应蛋白水平较低(16.53 mg/L vs. 33.94 mg/L, P < 0.05),住院率较低(26.23% vs. 42.86%, P < 0.05)。这些差异可能是由于抗炎基因gogB在s. 1,4,[5],12:i:-中携带率高(95.08% vs. 16.67%, P < 0.0001)。此外,S.1,4,[5],12:i:-对多种抗生素的耐药率高于传统的鼠伤寒沙门氏菌(32.79% vs. 7.14%, P < 0.001),尤其是头孢曲松。这种增加的抗性可能与携带IncHI2/IncHI2A质粒有关。该地区流行的s .1,4,[5],12:i:- ST34无性系与全球流行趋势一致,但具有较大的遗传多样性。总的来说,低炎症和高抵抗的隐形进化适应为这种变异的全球主导地位提供了新的见解。这些发现强调了提高临床意识和有针对性干预的重要性,特别是对弱势儿科人群。1,4, bbb,12:i:-对全球健康构成日益严重的威胁,尤其危及婴儿和幼儿。这种变异的特点是患病率上升、耐多药和诊断困难,在儿童感染中,与传统的鼠伤寒沙门氏菌相比,炎症反应较轻,但抗生素耐药性较强。关键是,我们确定了其独特的“低炎症,高抗性”进化策略与抗炎基因gogB和抗性质粒IncHI2/IncHI2A相关。这种隐秘的进化适应为这种变异的全球主导地位提供了新的见解,同时为改善临床管理和制定有针对性的公共卫生措施提供了重要指导,以保护脆弱的儿科人群免受这种狡猾病原体的侵害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evolutionary adaptations of a pediatric pathogen: low-inflammatory and high-resistance phenotypes in the emerging Salmonella typhimurium monophasic variant 1,4,[5],12:i:.

Salmonella enterica serovar 1,4,[5],12:i:- (S.1,4,[5],12:i:-), a monophasic variant of Salmonella typhimurium (S. typhimurium), is an emerging multidrug-resistant pathogen posing a significant threat to pediatric health. Research on this variant remains limited, and due to challenges associated with traditional identification methods, S.1,4,[5],12:i:- has often been misclassified as S. typhimurium. This study collected clinical data from 122 children infected with S.1,4,[5],12:i:- and 42 with traditional S. typhimurium in Fujian Province, China, between 2014 and 2023. Whole-genome sequencing was used for strain analysis. Our findings revealed that 77.87% of children with S.1,4,[5],12:i:- infection were aged between 1 month and 2 years. Compared with traditional S. typhimurium, children with S.1,4,[5],12:i:- exhibited milder clinical symptoms, as evidenced by lower levels of the inflammatory marker C-reactive protein (16.53 mg/L vs. 33.94 mg/L, P < 0.05) and a lower hospitalization rate (26.23% vs. 42.86%, P < 0.05). These differences may be attributed to the high carriage rate of the anti-inflammatory gene gogB in S.1,4,[5],12:i:- (95.08% vs. 16.67%, P < 0.0001). Additionally, S.1,4,[5],12:i:- exhibited a higher resistance rate to multiple antibiotics, particularly ceftriaxone, than traditional S. typhimurium (32.79% vs. 7.14%, P < 0.001). This increased resistance may be associated with the carriage of the IncHI2/IncHI2A plasmid. The S.1,4,[5],12:i:- ST34 clone prevalent in this region aligns with the global epidemic trend but exhibits greater genetic diversity. Overall, the stealthy evolutionary adaptation of low-inflammation and high-resistance provides novel insights into this variant's global dominance. These findings underscore the importance of heightened clinical awareness and targeted interventions, particularly for vulnerable pediatric populations.IMPORTANCES.1,4,[5],12:i:- poses a growing global health threat, particularly endangering infants and young children. Characterized by increasing prevalence, multidrug resistance, and diagnostic challenges, this variant demonstrates milder inflammatory responses yet stronger antibiotic resistance than traditional S. typhimurium in pediatric infections. Crucially, we identified its unique "low-inflammation, high-resistance" evolutionary strategy associated with anti-inflammatory gene gogB and resistance plasmid IncHI2/IncHI2A. The stealthy evolutionary adaptation provides novel insights into this variant's global dominance, while offering critical guidance for improving clinical management and formulating targeted public health measures to protect vulnerable pediatric populations against this cunning pathogen.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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