Manjate Filomena, João Eva D, Mwangi Peter, Chirinda Percina, Mogotsi Milton, Garrine Marcelino, Messa Augusto, Vubil Delfino, Nobela Nélio, Kotloff Karen, Nataro James P, Nhampossa Tacilta, Acácio Sozinho, Weldegebriel Goitom, Tate Jacqueline E, Parashar Umesh, Mwenda Jason M, Alonso Pedro L, Cunha Celso, Nyaga Martin, Mandomando Inácio
Centro de Investigação em Saúde de Manhiça (CISM), Maputo, Mozambique.
Global Health and Tropical Medicine, GHTM, Associate Laboratory in Translation and Innovation Towards Global Health, LA-REAL, Instituto de Higiene e Medicina Tropical, IHMT, Universidade NOVA de Lisboa, UNL, Rua da Junqueira 100, 1349-008, Lisboa, Portugal.
Sci Rep. 2024 Dec 28;14(1):30705. doi: 10.1038/s41598-024-79767-4.
Post rotavirus vaccine introduction in Mozambique (September 2015), we documented a decline in rotavirus-associated diarrhoea and genotypes changes in our diarrhoeal surveillance spanning 2008-2021. This study aimed to perform whole-genome sequencing of rotavirus strains from 2009 to 2012 (pre-vaccine) and 2017-2018 (post-vaccine). Rotavirus strains previously detected by conventional PCR as G2P[4], G2P[6], G3P[4], G8P[4], G8P[6], and G9P[6] from children with moderate-to-severe and less-severe diarrhoea and without diarrhoea (healthy community controls) were sequenced using Illumina MiSeq platform and analysed using bioinformatics tools. All these G and P-type combinations exhibited DS-1-like constellation in the rest of the genome segments as, I2-R2-C2-M2-A2-N2-T2-E2-H2. Phylogenetic analysis revealed that strains from children with and without diarrhoea clustered together with other Mozambican and global strains. Notably, the NSP4 gene of strains G3P[4] and G8P[4] in children with diarrhoea clustered with animal strains, such as bovine and caprine, with similarity identities ranging from 89.1 to 97.0% nucleotide and 89.5-97.0% amino acids. Our findings revealed genetic similarities among rotavirus strains from children with and without diarrhoea, as well as with animal strains, reinforcing the need of implementing studies with One Health approach in our setting, to elucidate the genetic diversity of this important pathogen.
在莫桑比克引入轮状病毒疫苗后(2015年9月),我们记录了2008年至2021年腹泻监测中轮状病毒相关腹泻的下降以及基因型变化。本研究旨在对2009年至2012年(疫苗接种前)和2017年至2018年(疫苗接种后)的轮状病毒株进行全基因组测序。先前通过常规PCR检测到的来自中重度腹泻、轻度腹泻儿童以及无腹泻儿童(健康社区对照)的G2P[4]、G2P[6]、G3P[4]、G8P[4]、G8P[6]和G9P[6]型轮状病毒株,使用Illumina MiSeq平台进行测序,并使用生物信息学工具进行分析。所有这些G型和P型组合在基因组的其他片段中均呈现出类似DS-1的星座模式,即I2-R2-C2-M2-A2-N2-T2-E2-H2。系统发育分析表明,腹泻儿童和无腹泻儿童的毒株与其他莫桑比克及全球毒株聚集在一起。值得注意的是,腹泻儿童中G3P[4]和G8P[4]毒株的NSP4基因与牛和山羊等动物毒株聚集在一起,核苷酸相似性为89.1%至97.0%,氨基酸相似性为89.5%至97.0%。我们的研究结果揭示了腹泻儿童和无腹泻儿童的轮状病毒株之间以及与动物毒株之间的遗传相似性,强化了在我们的环境中采用“同一健康”方法开展研究以阐明这一重要病原体遗传多样性的必要性。