Higher frequency of interstate over international transmission chains of SARS-CoV-2 virus at the Rio Grande do Sul - Brazil state borders.

IF 2.5 4区 医学 Q3 VIROLOGY
Virus research Pub Date : 2025-01-01 Epub Date: 2024-12-17 DOI:10.1016/j.virusres.2024.199500
Filipe Zimmer Dezordi, José Valter Joaquim Silva Júnior, Terimar Facin Ruoso, Angela Giovana Batista, Pedro Mesquita Fonseca, Larissa Paim Bernardo, Richard Steiner Salvato, Tatiana Schäffer Gregianini, Thaísa Regina Rocha Lopes, Eduardo Furtado Flores, Rudi Weiblen, Patrícia Chaves Brites, Mônica de Medeiros Silva, João Batista Teixeira da Rocha, Gustavo de Lima Barbosa, Lais Ceschini Machado, Alexandre Freitas da Silva, Marcelo Henrique Santos Paiva, Matheus Filgueira Bezerra, Tulio de Lima Campos, Tiago Gräf, Daniel Angelo Sganzerla Graichen, Elgion Lucio da Silva Loreto, Gabriel da Luz Wallau
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引用次数: 0

Abstract

Brazil's COVID-19 response has faced challenges due to the continuous emergence of variants of concern (VOCs), emphasizing the need for ongoing genomic surveillance and retrospective analyses of past epidemic waves to reassess and fine tune containment protocols. Rio Grande do Sul (RS), Brazil's southernmost state, has international borders and trades with Argentina and Uruguay, along with significant domestic connections within Brazil. The identification of source and sink transmission chains at national and international scales can identify main hubs and pathways to target future interventions. In this study we investigated the RS state role in the national and international SARS-CoV-2 transmission chains, which has not been fully explored. Nasopharyngeal samples from various municipalities in RS were collected between June 2020 and July 2022. SARS-CoV-2 whole genome amplification and sequencing were performed using high-throughput Illumina sequencing. Bioinformatics analysis encompassed the development of scripts and tools to perform subsampling taking into account epidemiological information to reduce sequencing disparities bias among the regions/countries, genome assembly, and large-scale alignment and phylogenetic reconstruction. We sequenced a total of 1,480 SARS-CoV-2 genomes from RS, covering all major regions. Sequences predominantly represented Gamma (April-June 2021) and Omicron (January-July 2022) lineages. Phylogenetic analysis revealed a regional pattern for transmission dynamics, particularly with Southeast Brazil for Gamma, and a range of inter-regional connections for Delta and Omicron within the country. On the other hand, international and cross-border transmission with Argentina and Uruguay was rather limited. We evaluated the three VOCs circulation over two years in RS using a new subsampling strategy based on the number of cases in each state during the circulation of each VOC. In summary, the retrospective analysis of genomic surveillance data demonstrated that virus transmission was less intense between country borders than within the country. These findings suggest that while non-pharmacological interventions were effective to mitigate transmission across international RS land borders, they were insufficient to contain transmission at the domestic level.

在巴西南部大德州边境,州际间SARS-CoV-2病毒的国际传播链频率更高。
由于关注变异物(VOCs)的不断出现,巴西的COVID-19应对工作面临挑战,这突显出需要持续进行基因组监测和对过去流行波进行回顾性分析,以重新评估和微调遏制方案。南大州(RS)是巴西最南端的州,与阿根廷和乌拉圭接壤,并与阿根廷和乌拉圭进行贸易,同时在巴西境内也有重要的国内联系。在国家和国际范围内确定源和汇传播链可以确定主要枢纽和途径,以确定未来干预措施的目标。在这项研究中,我们调查了RS国家在国家和国际SARS-CoV-2传播链中的作用,这一点尚未得到充分探讨。在2020年6月至2022年7月期间收集了RS各城市的鼻咽样本。采用高通量Illumina测序技术进行SARS-CoV-2全基因组扩增和测序。生物信息学分析包括基于流行病学信息的亚采样脚本和工具的开发,以减少区域/国家之间的测序差异偏差,基因组组装,大规模比对和系统发育重建。我们对来自RS的1480个SARS-CoV-2基因组进行了测序,覆盖了所有主要区域。序列主要代表Gamma(2021年4月至6月)和Omicron(2022年1月至7月)谱系。系统发育分析揭示了传播动态的区域模式,特别是Gamma在巴西东南部,Delta和Omicron在国内有一系列区域间联系。另一方面,阿根廷和乌拉圭之间的国际和跨境传播相当有限。我们根据每个州在每种挥发性有机化合物流通期间的病例数,采用一种新的子抽样策略评估了RS两年内三种挥发性有机化合物的流通。总之,对基因组监测数据的回顾性分析表明,病毒在国与国之间的传播不如在国内传播那么严重。这些发现表明,虽然非药物干预措施可以有效地减轻RS跨越国际陆地边界的传播,但它们不足以在国内层面遏制传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Virus research
Virus research 医学-病毒学
CiteScore
9.50
自引率
2.00%
发文量
239
审稿时长
43 days
期刊介绍: Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.
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