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基因组分析揭示了 S. Paratyphi A 谱系出现和持续存在中的基因组退化事件和基因流。

Genomic analysis unveils genome degradation events and gene flux in the emergence and persistence of S. Paratyphi A lineages.

机构信息

Christian Medical College, Vellore, India.

REVA University, Bangalore, India.

出版信息

PLoS Pathog. 2023 Apr 28;19(4):e1010650. doi: 10.1371/journal.ppat.1010650. eCollection 2023 Apr.

Abstract

Paratyphoid fever caused by S. Paratyphi A is endemic in parts of South Asia and Southeast Asia. The proportion of enteric fever cases caused by S. Paratyphi A has substantially increased, yet only limited data is available on the population structure and genetic diversity of this serovar. We examined the phylogenetic distribution and evolutionary trajectory of S. Paratyphi A isolates collected as part of the Indian enteric fever surveillance study "Surveillance of Enteric Fever in India (SEFI)." In the study period (2017-2020), S. Paratyphi A comprised 17.6% (441/2503) of total enteric fever cases in India, with the isolates highly susceptible to all the major antibiotics used for treatment except fluoroquinolones. Phylogenetic analysis clustered the global S. Paratyphi A collection into seven lineages (A-G), and the present study isolates were distributed in lineages A, C and F. Our analysis highlights that the genome degradation events and gene acquisitions or losses are key molecular events in the evolution of new S. Paratyphi A lineages/sub-lineages. A total of 10 hypothetically disrupted coding sequences (HDCS) or pseudogenes-forming mutations possibly associated with the emergence of lineages were identified. The pan-genome analysis identified the insertion of P2/PSP3 phage and acquisition of IncX1 plasmid during the selection in 2.3.2/2.3.3 and 1.2.2 genotypes, respectively. We have identified six characteristic missense mutations associated with lipopolysaccharide (LPS) biosynthesis genes of S. Paratyphi A, however, these mutations confer only a low structural impact and possibly have minimal impact on vaccine effectiveness. Since S. Paratyphi A is human-restricted, high levels of genetic drift are not expected unless these bacteria transmit to naive hosts. However, public-health investigation and monitoring by means of genomic surveillance would be constantly needed to avoid S. Paratyphi A serovar becoming a public health threat similar to the S. Typhi of today.

摘要

甲型副伤寒由甲型副伤寒沙门氏菌引起,在南亚和东南亚部分地区流行。由甲型副伤寒沙门氏菌引起的肠热病病例比例大幅增加,但关于该血清型的种群结构和遗传多样性的资料有限。我们研究了作为印度肠热病监测研究“印度肠热病监测(SEFI)”一部分收集的甲型副伤寒沙门氏菌分离株的系统发育分布和进化轨迹。在研究期间(2017-2020 年),甲型副伤寒沙门氏菌占印度总肠热病病例的 17.6%(441/2503),其分离株对除氟喹诺酮类药物外所有主要治疗抗生素高度敏感。系统发育分析将全球甲型副伤寒沙门氏菌集落分为七个谱系(A-G),本研究分离株分布在谱系 A、C 和 F 中。我们的分析强调,基因组退化事件和基因获得或丢失是新甲型副伤寒沙门氏菌谱系/亚谱系进化的关键分子事件。共鉴定出 10 个可能与谱系出现相关的假设破坏编码序列(HDCS)或假基因形成突变。全基因组分析确定了 P2/PSP3 噬菌体的插入和 IncX1 质粒的获得,分别在 2.3.2/2.3.3 和 1.2.2 基因型中选择。我们已经确定了与甲型副伤寒沙门氏菌脂多糖(LPS)生物合成基因相关的六个特征错义突变,但这些突变仅赋予结构上的低影响,并且可能对疫苗效果的影响最小。由于甲型副伤寒沙门氏菌仅在人类中传播,除非这些细菌传播到无免疫力的宿主,否则预计不会出现高水平的遗传漂移。然而,需要通过基因组监测进行公共卫生调查和监测,以避免甲型副伤寒沙门氏菌血清型成为类似于今天的伤寒沙门氏菌的公共卫生威胁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/12c5/10171690/76ae45f55fc5/ppat.1010650.g001.jpg

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