2024-2025年中国II型PRRSV分子流行病学、谱系进化动力学及抗原变异分析

IF 3 2区 农林科学 Q2 INFECTIOUS DISEASES
Dihua Zhu, Guangyu Liu, Huixin Li, Fen Li, Xiaolong Xu, Yuanyuan Fu, Pandan Chen, Guihong Zhang, Yankuo Sun
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引用次数: 0

摘要

猪繁殖与呼吸综合征病毒(PRRSV)是全球养猪业的主要威胁之一,其快速进化和抗原变异给疾病控制带来了持续的挑战。本研究基于中国27个省份2024-2025年间收集的328例PRRSV症状猪(呼吸系统疾病、繁殖衰竭和高热)临床样本,采用开放阅读框(ORF) 5基因测序、关键谱系(包括快速传播的nadc30样谱系1.8株、疫苗相关谱系8.7株和遗传上不同的谱系3株)代表性菌株的全基因组测序、系统发育分析、传播动力学分析、宿主内单核苷酸变异(iSNV)分析和重组检测,系统揭示目前在中国流行的II型PRRSV的分子流行病学特征和进化动力学。结果表明,中国ⅱ型PRRSV病毒在1.5、1.8、3、5、8.7 5个主要世系中存在复杂的共存模式,其中以1.8为主要流行株(48.5%),其次为1.5(23.2%),而3、5、8.7世系的地理分布较为有限。空间传播分析发现,广东和河南是关键传播节点,形成了连接南北的“病毒交换中心”,湖北、山西和江苏成为新的病毒聚集点。遗传多样性分析显示,除Lineage 5外,所有世系均具有较高的单倍型多样性(Hd),其中Lineage 5的核苷酸多样性在1年内显著增加106.6%,表明其具有快速的适应性进化。Tajima的D检验结果显示大多数谱系为阴性,谱系5和8.7达到统计学意义,表明这些病毒群体最近经历了群体扩张或定向选择。基于遗传距离的多维尺度(MDS)分析显示,主要流行谱系(1.8和3)与当前疫苗株之间存在潜在的抗原差异,这可能会影响疫苗的效力。对三个代表性基因组的深入分析揭示了涉及疫苗相关菌株的复杂重组模式,并确定ORF2-ORF3区域是潜在的重组热点。本研究结果为了解中国II型PRRSV的进化机制提供了科学依据,为制定有针对性的控制策略和优化疫苗设计提供了重要参考,对确保后非洲猪瘟时代中国养猪业的健康发展具有重要价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Epidemiology, Lineage Evolutionary Dynamics, and Antigenic Variation Analysis of Type II PRRSV in China During 2024–2025

Molecular Epidemiology, Lineage Evolutionary Dynamics, and Antigenic Variation Analysis of Type II PRRSV in China During 2024–2025

Porcine reproductive and respiratory syndrome virus (PRRSV) represents one of the major threats to the global swine industry, with its rapid evolution and antigenic variation posing persistent challenges to disease control. Based on 328 clinical samples collected from PRRSV symptomatic (respiratory disorders, reproductive failures, and high fever) pigs across 27 provinces in China during 2024–2025, this study employed open reading frame (ORF) 5 gene sequencing, complete genome sequencing of representative strains from key lineages (including a rapidly spreading NADC30-like Lineage 1.8 strain, a vaccine-related Lineage 8.7 strain, and a genetically distinct Lineage 3 strain), phylogenetic analysis, transmission dynamics analysis, intrahost single nucleotide variant (iSNV) analysis, and recombination detection to systematically reveal the molecular epidemiological characteristics and evolutionary dynamics of type II PRRSV currently circulating in China. The results demonstrated a complex pattern of coexistence among five major lineages of type II PRRSV in China, including Lineage 1.5, Lineage 1.8, Lineage 3, Lineage 5, and Lineage 8.7, with Lineage 1.8 emerging as the predominant circulating strain (48.5% of positive samples), followed by Lineage 1.5 (23.2%), while Lineages 3, 5, and 8.7 showed more restricted geographical distribution. Spatial transmission analysis identified Guangdong and Henan as key transmission nodes, forming “viral exchange centers” connecting northern and southern regions, while Hubei, Shanxi, and Jiangsu have become new viral aggregation sites. Genetic diversity analysis revealed high haplotype diversity (Hd) across all lineages except Lineage 5, with Lineage 5 showing a remarkable 106.6% increase in nucleotide diversity within 1 year, indicating rapid adaptive evolution. Tajima’s D test results revealed negative values for most lineages, with Lineage 5 and 8.7 reaching statistical significance, suggesting these viral populations have undergone recent population expansion or directional selection. Multidimensional scaling (MDS) analysis based on genetic distance revealed a potential antigenic divergence between the predominant circulating lineages (1.8 and 3) and current vaccine strains, which may compromise vaccine efficacy. In-depth analysis of three representative genomes revealed complex recombination patterns involving vaccine-related strains and identified the ORF2-ORF3 region as a potential recombination hotspot. The findings of this study provide a scientific basis for understanding the evolutionary mechanisms of type II PRRSV in China and offer important references for formulating targeted control strategies and optimizing vaccine design, which has significant value for ensuring the healthy development of China’s swine industry in the post-African swine fever era.

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来源期刊
Transboundary and Emerging Diseases
Transboundary and Emerging Diseases 农林科学-传染病学
CiteScore
8.90
自引率
9.30%
发文量
350
审稿时长
1 months
期刊介绍: Transboundary and Emerging Diseases brings together in one place the latest research on infectious diseases considered to hold the greatest economic threat to animals and humans worldwide. The journal provides a venue for global research on their diagnosis, prevention and management, and for papers on public health, pathogenesis, epidemiology, statistical modeling, diagnostics, biosecurity issues, genomics, vaccine development and rapid communication of new outbreaks. Papers should include timely research approaches using state-of-the-art technologies. The editors encourage papers adopting a science-based approach on socio-economic and environmental factors influencing the management of the bio-security threat posed by these diseases, including risk analysis and disease spread modeling. Preference will be given to communications focusing on novel science-based approaches to controlling transboundary and emerging diseases. The following topics are generally considered out-of-scope, but decisions are made on a case-by-case basis (for example, studies on cryptic wildlife populations, and those on potential species extinctions): Pathogen discovery: a common pathogen newly recognised in a specific country, or a new pathogen or genetic sequence for which there is little context about — or insights regarding — its emergence or spread. Prevalence estimation surveys and risk factor studies based on survey (rather than longitudinal) methodology, except when such studies are unique. Surveys of knowledge, attitudes and practices are within scope. Diagnostic test development if not accompanied by robust sensitivity and specificity estimation from field studies. Studies focused only on laboratory methods in which relevance to disease emergence and spread is not obvious or can not be inferred (“pure research” type studies). Narrative literature reviews which do not generate new knowledge. Systematic and scoping reviews, and meta-analyses are within scope.
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