Kartashov Mikhail Yu, Krivosheina Ekaterina I, Naidenova Ekaterina V, Zakharov Kirill S, Shvalov Alexander N, Boumbaly Sanaba, Ternovoi Vladimir A, Loktev Valery B
Department of Molecular Virology for Flaviviruses and Viral Hepatitis, Rospotrebnadzor, Novosibirsk, Russia.
Novosibirsk National Research State University, Novosibirsk, Russia.
Vector Borne Zoonotic Dis. 2025 Jul;25(7):470-475. doi: 10.1089/vbz.2024.0056. Epub 2025 May 23.
Over the past decade, numerous new tick-associated flavi-like viruses with segmented genomes have been discovered almost worldwide. Kindia tick virus (KITV) was first detected in ticks in West Africa in 2017. The current study aimed to detect viral RNA in tick and cattle samples collected in Guinea and to perform complete sequencing of KITV isolates and their analysis. Adult ticks and blood samples were collected from cattle in Coyah, Dubréka, Forécariah, and Kindia prefectures of the Republic of Guinea in 2022. These samples were tested for KITV infection by RT-PCR with primers targeting the NS5 gene. Positive probes were sequenced using Illumina technology, and their analysis was performed for obtaining complete sequences of all KITV segments. The RNA of the KITV was detected by RT-PCR in , ticks, and blood samples of cattle. The prevalence rates for cattle were 6.6%, for 6.9%, and for ticks 10.7%. The analysis of 15 complete sequences of KITV genomes showed 99.61-99.67% identity for amino acid sequences for segments 1 and 4 and 97.88-98.83% for segments 2 and 3 with previously detected KITV isolate in Guinea in 2017. Phylogenetic analysis demonstrated that obtained KITV sequences can be classified as typical for clade A of the Jingmen tick virus (JMTV) group together with Mogiana tick virus. The KITV isolates from cattle and feeding ticks show practically full identity sequences for all four viral segments, and these sequences can be classified as clade A of the segmented flavi-like virus JMTV group.
在过去十年中,几乎在全球范围内发现了许多新的与蜱相关的具有分段基因组的黄病毒样病毒。金迪亚蜱病毒(KITV)于2017年首次在西非的蜱中被检测到。当前的研究旨在检测在几内亚采集的蜱和牛样本中的病毒RNA,并对KITV分离株进行全序列测序及分析。2022年,从几内亚共和国科亚、杜布雷卡、福雷卡里亚和金迪亚等省的牛身上采集了成年蜱和血液样本。使用靶向NS5基因的引物通过RT-PCR对这些样本进行KITV感染检测。阳性样本使用Illumina技术进行测序,并对其进行分析以获得所有KITV片段的完整序列。通过RT-PCR在牛的蜱和血液样本中检测到了KITV的RNA。牛的感染率为6.6%,蜱的感染率为6.9%,而蜱虫的感染率为10.7%。对15个KITV基因组完整序列的分析表明,与2017年在几内亚先前检测到的KITV分离株相比,第1和第4片段的氨基酸序列同一性为99.61 - 99.67%,第2和第3片段的同一性为97.88 - 98.83%。系统发育分析表明,获得的KITV序列可与莫吉亚纳蜱病毒一起归类为荆门蜱病毒(JMTV)组A分支的典型序列。从牛和取食蜱中分离出的KITV在所有四个病毒片段上显示出几乎完全相同的序列,并且这些序列可归类为分段黄病毒样病毒JMTV组的A分支。