不同TMEM154基因型细胞系对不同SRLV基因型/亚型的许可性

IF 3.8 2区 医学 Q2 VIROLOGY
Journal of Virology Pub Date : 2025-09-23 Epub Date: 2025-08-22 DOI:10.1128/jvi.00961-25
Barbara Colitti, Daniele Avanzato, Riccardo Moretti, Irati Moncayola, Margherita Profiti, Stefania Chessa, Paola Sacchi, Sergio Rosati, Ramses Reina
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引用次数: 0

摘要

小反刍慢病毒(srlv)是一种异质病毒群,在世界范围内感染山羊和绵羊,目前尚无治疗方法或有效疫苗。控制措施以早期诊断和准确管理为基础,但由于在受控制的鸡群中再次出现血清阳性和疾病,控制措施取得的成效有限。绵羊跨膜154 (TMEM154)基因的遗传变异与对某些病毒亚型的易感性之间存在关联,这可能是降低绵羊感染流行的一种控制策略。因此,鉴定TMEM154基因型中E35K SNP对SRLV亚型的抗性谱变得至关重要。在这项研究中,来自动物的10种皮肤成纤维细胞系编码TMEM154 (E35K) SNP的三种基因型,被8种SRLV病毒株感染,并检测逆转录酶(RT)活性和细胞病变效应的存在。此外,使用病毒假型评估SRLV进入细胞的情况。8个病毒株中有2个在纯合子KK细胞系的上清中表现出较少的合胞体,细胞融合程度降低,RT活性降低,表明这些细胞存在抗性模式。进入实验显示,在8株菌株中,有7株在3株细胞系之间存在统计学上的显著差异,表明进入阻断是KK细胞的主要限制因素。这些发现支持了TMEM154基因作为对特定SRLV亚型具有抗性的动物进行遗传选择的标记的潜在用途。此外,体外方法被证明是研究不同SRLV菌株抗性模式的有价值的工具。小型反刍动物慢病毒是一种全球传播的病原体,影响动物健康并造成严重的经济损失。考虑到这些病毒的高遗传和抗原变异性以及缺乏有效的治疗方法或疫苗,基于TMEM154基因的耐药动物的遗传选择代表了控制感染的有趣机会。因此,本研究旨在利用体外模型进一步研究宿主-病原体相互作用,考虑到保护性突变的动物基因型与感染病毒基因型之间的关系。研究证实,TMEM154基因变异是SRLV特定菌株(包括高致病性B1亚型)对SRLV易感性的有益预测因素,而对某些a和B2亚型的易感性不受TMEM154基因的影响。这再次强调了通过遗传选择程序监测循环病毒变异对有效控制SRLV感染的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Permissiveness of different TMEM154 genotype cell lines to different SRLV genotypes/subtypes.

Small ruminant lentiviruses (SRLVs) are a heterogeneous group of viruses that infect goats and sheep worldwide, for which no cures or effective vaccines are available. Control measures have been based on early diagnosis and accurate management with limited success due to re-emergence of seropositivity and disease in controlled flocks. Association between the genetic variation in the ovine transmembrane 154 (TMEM154) gene and susceptibility to certain viral subtypes was previously demonstrated, representing a possible control strategy to reduce infection prevalence in sheep. Thus, the identification of the resistance spectrum of E35K SNP within TMEM154 genotypes toward SRLV subtypes becomes crucial. In this study, 10 skin fibroblastic cell lines, from animals encoding three genotypes of the TMEM154 (E35K) SNP, were infected with 8 SRLV viral strains and tested for the presence of retrotranscriptase (RT) activity and cytopathic effect. Additionally, SRLV entry into cells was evaluated using viral pseudotypes. Two out of the eight viral strains showed fewer syncytia, reduced cell fusion degree, and lower RT activity in the supernatant of homozygous KK cell lines, suggesting a resistant pattern in these cells. The entry assay revealed a statistically significant difference between the three cell lines in seven of the eight strains, suggesting an entry blockade as the primary restriction factor in KK cells. These findings support the potential use of the TMEM154 gene as a marker for the genetic selection of resistant animals to specific SRLV subtypes. Moreover, the ex vivo approach was validated as a valuable tool for studying resistance patterns against different SRLV strains.IMPORTANCESmall ruminant lentiviruses are worldwide spread pathogens that impact animal health and result in severe economic losses. Considering the high genetic and antigenic variability of these viruses and the absence of an effective cure or vaccine, the genetic selection of resistant animals based on the TMEM154 gene represents an interesting opportunity to control the infection. Thus, this study aimed to investigate further the host-pathogen interaction considering the association between the animal genotype for the suggested protective mutation and the infecting virus genotype using an in vitro model. The study confirmed TMEM154 genetic variation as a helpful predictive factor for SRLV susceptibility by particular SRLV strains including the highly pathogenic B1 subtype, while susceptibility to some A and the B2 subtypes was not affected by the TMEM154 gene. Once more, it highlighted the importance of monitoring circulating viral variants for the effective control of SRLV infection through genetic selection programs.

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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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