在蜱媒脑炎高发区立陶宛捕获的野生啮齿动物中蜱媒脑炎病毒的流行情况

Viruses Pub Date : 2024-03-13 DOI:10.3390/v16030444
Evelina Simkute, Arnoldas Pautienius, Juozas Grigas, Marina Sidorenko, Jana Radzijevskaja, Algimantas Paulauskas, Arunas Stankevicius
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引用次数: 0

摘要

野生啮齿类动物被认为是最重要的 TBEV 扩增库宿主之一,因此适合用于病灶检测研究。为了研究在野生啮齿类动物中检测病毒 RNA 对确认疑似 TBEV 病灶的有效性,我们在立陶宛多个地方诱捕了小型啮齿类动物(n = 139),这些地方以前曾在蜱虫中检测到过 TBEV。每份啮齿动物样本都接种了小鼠神经母细胞瘤 Neuro-2a 细胞,以最大限度地提高在啮齿动物样本中检测到病毒 RNA 的几率。在74.8%(CI 95% 66.7-81.1)的脑和/或内脏混合悬液中检测到了TBEV RNA,样本在Neuro-2a细胞中培养后,TBEV RNA的流行率显著增加。此外,诱捕啮齿动物时的月平均气温与啮齿动物悬浮液细胞培养分离物中 TBEV RNA 的流行率之间存在很强的相关性(r = 0.88; p < 0.05),而这些分离物在细胞培养前 PCR 阴性。这项研究表明,野生啮齿动物是确认 TBEV 病灶的合适哨点动物。此外,研究结果还表明,细胞培养样本是一种高效的方法,可将 TBEV 病毒载量提高到可检测的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Prevalence of Tick-Borne Encephalitis Virus in Wild Rodents Captured in Tick-Borne Encephalitis Foci in Highly Endemic Lithuania
Wild rodents are considered to be one of the most important TBEV-amplifying reservoir hosts; therefore, they may be suitable for foci detection studies. To investigate the effectiveness of viral RNA detection in wild rodents for suspected TBEV foci confirmation, we trapped small rodents (n = 139) in various locations in Lithuania where TBEV was previously detected in questing ticks. Murine neuroblastoma Neuro-2a cells were inoculated with each rodent sample to maximize the chances of detecting viral RNA in rodent samples. TBEV RNA was detected in 74.8% (CI 95% 66.7–81.1) of the brain and/or internal organ mix suspensions, and the prevalence rate increased significantly following sample cultivation in Neuro-2a cells. Moreover, a strong correlation (r = 0.88; p < 0.05) was found between the average monthly air temperature of rodent trapping and the TBEV RNA prevalence rate in cell culture isolates of rodent suspensions, which were PCR-negative before cultivation in cell culture. This study shows that wild rodents are suitable sentinel animals to confirm TBEV foci. In addition, the study results demonstrate that sample cultivation in cell culture is a highly efficient method for increasing TBEV viral load to detectable quantities.
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