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Liquid-liquid phase separation in the viral replication cycle: new paradigms and therapeutic opportunities. 病毒复制周期中的液-液相分离:新范例和治疗机会。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-20 DOI: 10.1007/s00705-026-06607-3
Fnu Sanjida, Md Imran Hossain, Sajidur Rahman Akash, Md Sarafat Ali
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引用次数: 0
Agave associated crinivirus A: a novel monopartite crinivirus homolog isolated from agave. 龙舌兰相关犯罪病毒A:从龙舌兰中分离出的一种新的单株犯罪病毒同源物。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-20 DOI: 10.1007/s00705-026-06580-x
Kristian A Stevens, Juliana Osse de Souza, Haoran Li, Ashrafou Ouro-Djobo, Olufemi J Alabi, Maher Al Rwahnih
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引用次数: 0
Deciphering cassava brown streak virus infection in cassava through VPg mediated host protein interactions. 通过VPg介导的宿主蛋白相互作用解读木薯褐条病毒感染。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-19 DOI: 10.1007/s00705-026-06571-y
Sumesh M Kakkunnath, Sophie Bouvaine, Siji P Kavil, M N Maruthi

Cassava brown streak disease (CBSD) poses a major threat to cassava production in Africa. Identifying cassava proteins that interact with cassava brown streak virus (CBSV), the major causal virus, can help elucidate the mechanisms of infection and resistance. Here we constructed a cassava cDNA library and screened for proteins interacting with CBSV viral genome-linked protein (VPg) using yeast two-hybrid assays, identifying 36 interactors. Four candidates were validated in Nicotiana benthamiana via bimolecular fluorescence complementation. Functional categories included chloroplast proteins, ribosomal components, chaperones, metabolic enzymes, and defence-related proteins. In prior RNA-seq datasets from CBSV or UCBSV-inoculated cassava, comprising the susceptible variety Albert and the resistant variety Namikonga, 16 VPg-interacting genes were identified among the differentially expressed genes (|log₂FC| > 1), with 2 detected in Albert and 15 in Namikonga. These results indicate that VPg-interacting host proteins are involved in CBSV infection dynamics and also explaining the differential responses of resistant and susceptible cassava varieties, thus offering potential new molecular targets for CBSD management.

木薯褐条病(CBSD)对非洲木薯生产构成重大威胁。鉴定与主要致病病毒木薯褐条病毒(CBSV)相互作用的木薯蛋白,可以帮助阐明感染和抗性的机制。本研究构建了木薯cDNA文库,并利用酵母双杂交技术筛选了与CBSV病毒基因组连接蛋白(VPg)相互作用的蛋白,共鉴定出36个相互作用蛋白。通过双分子荧光互补,对4个候选物质进行了benthamiana中的验证。功能分类包括叶绿体蛋白、核糖体成分、伴侣蛋白、代谢酶和防御相关蛋白。在CBSV或ucbsv接种木薯(包括易感品种Albert和抗性品种Namikonga)的RNA-seq数据中,在差异表达基因(|log₂FC| > 1)中鉴定出16个vpg相互作用基因,其中Albert和Namikonga分别检测到2个和15个。这些结果表明,vpg相互作用的宿主蛋白参与了CBSV感染动力学,并解释了抗性和易感木薯品种的差异反应,从而为CBSD管理提供了潜在的新分子靶点。
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引用次数: 0
Viral subversion of neddylation: dual roles in replication efficiency and evasion of antiviral immunity. 病毒颠覆类化修饰:在复制效率和逃避抗病毒免疫中的双重作用。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-19 DOI: 10.1007/s00705-026-06566-9
Xiaoli Mo, Bohan Yu, Xudong Tang
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引用次数: 0
Enhancing the immunogenicity of a recombinant PEDV subunit vaccine: the role of lipoprotein signal peptide. 提高重组PEDV亚单位疫苗的免疫原性:脂蛋白信号肽的作用。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-18 DOI: 10.1007/s00705-026-06568-7
Haroon Afzal, Muhammad Umar, Nguyen-Thanh Hoa, Guan-Ming Ke, Li-Ting Cheng
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引用次数: 0
Specific features of the infection caused by SARS-CoV-2 variants in Vero cell culture. Vero细胞培养中SARS-CoV-2变异引起感染的特异性特征
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-18 DOI: 10.1007/s00705-026-06551-2
Alexander Chepurnov, Svetlana Miroshnichenko, Mickhail Ivanov, Mariya Solomatina, Elena Kazachinskaia, Evgeniya Kazachkova, Yulia Kononova, Mickhail Voevoda, Arseniya Shelemba, Oksana Mishchenko, Aleksey Surovyatkin, Marina Gulyaeva, Alexander Shestopalov
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引用次数: 0
PEDV infection induces ferroptosis in Vero cells via an ACSL4-mediated lipid peroxidation pathway. PEDV感染通过acsl4介导的脂质过氧化途径诱导Vero细胞铁下垂。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-18 DOI: 10.1007/s00705-026-06586-5
Qian Weng, Yuheng Li, Yuze Wei, Simin Wang, Tingyu Hu, Zhihua Pei, Kai Wang, Guixue Hu
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引用次数: 0
Immune responses in chicken mucosal lymphoid tissues following oral and eye drop vaccination and revaccination with live modified vaccine of infectious laryngotracheitis virus (ILTV). 口服和滴眼液接种和再接种传染性喉气管炎病毒(ILTV)改性活疫苗后鸡粘膜淋巴组织的免疫应答
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-18 DOI: 10.1007/s00705-026-06560-1
Thanh Tien Tran, Nicholas M Andronicos, Natkunam Ketheesan, Stephen W Walkden-Brown, Priscilla F Gerber
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引用次数: 0
Microalga-virus-virophage coculture reveals co-infection of multi-virophages with a giant virus. 微藻-病毒-噬菌体共培养揭示了多种噬菌体与巨型病毒的共同感染。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-17 DOI: 10.1007/s00705-026-06547-y
Ting Chu, Qinran Wang, Chen Hu, Jiabei Yu, Lanming Chen, Yongxin Yu, Yongjie Wang

Virophages parasitize the replication of co-infecting giant viruses within eukaryotic cells, forming tripartite cell-virus-virophage (CVv) systems. Tripartite interactions are well-documented in protozoa, yet comparable systems in algae remain largely unexplored at the experimental level. Here, we report an experimentally validated CVv system involving the green, single-celled microalga Chlorella sp. DSL01, Dishui Lake large algal virus 1 (DSLLAV1), and multiple Dishui Lake virophages (DSLVs). Inoculation of Chlorella sp. DSL01 at low MOI established laboratory co-cultures in which time-series PCR detected DSLLAV1 early but not after Day 10, whereas all tested virophages persisted. Metagenomic profiling of the terminal supernatant (end-point sample) indicated a virophage-dominated assemblage with DSLV3 most represented. Droplet digital PCR at discrete time points (Days 5, 10, and 15) then provided absolute counts for DSLLAV1 and DSLV1/3/7, corroborating an early DSLLAV1 peak followed by collapse and/or a delayed rise of multiple virophages coincident with host growth recovery. Nested PCR on the algal pellet detected virophages DSLV1/3/7 but not DSLLAV1. Together, these results demonstrate that Chlorella sp. DSL01 supports co-infection by DSLLAV1 and multiple virophages, establishing an experimentally validated algal CVv system and revealing multi-virophage participation in freshwater algal virus-virophage-host dynamics.

噬菌体寄生于真核细胞内共感染巨病毒的复制体,形成三边细胞-病毒-噬菌体(CVv)系统。三方相互作用在原生动物中有很好的文献记载,但藻类的类似系统在实验水平上仍未被探索。在这里,我们报道了一个实验验证的CVv系统,涉及绿色,单细胞微藻小球藻sp. DSL01,滴水湖大藻病毒1 (DSLLAV1)和多个滴水湖病毒噬菌体(dslv)。在低MOI条件下接种小球藻DSL01建立了实验室共培养,时间序列PCR在早期检测到DSLLAV1,但在第10天之后没有检测到,而所有检测的病毒噬菌体都持续存在。末端上清(终点样本)的宏基因组分析表明,以DSLV3为代表的病毒噬菌体为主的组合。在离散时间点(第5、10和15天),液滴数字PCR提供了DSLLAV1和DSLV1/3/7的绝对计数,证实了DSLLAV1的早期峰值,随后崩溃和/或多个病毒噬菌体的延迟上升与宿主生长恢复一致。在藻球上嵌套PCR检测到噬菌体DSLV1/3/7,但未检测到DSLLAV1。上述结果表明,小球藻DSL01支持DSLLAV1与多种病毒噬菌体共同感染,建立了一个经过实验验证的藻类CVv系统,揭示了多种病毒噬菌体参与淡水藻类病毒-病毒噬菌体-宿主动力学过程。
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引用次数: 0
Correction: Lineage replacement of coxsackievirus A10 in Vietnam associated with increased detection and altered disease severity grading of hand, foot, and mouth disease. 更正:在越南,柯萨奇病毒A10的谱系替换与手足口病的检出率增加和疾病严重程度分级改变有关。
IF 2.5 4区 医学 Q3 VIROLOGY Pub Date : 2026-03-17 DOI: 10.1007/s00705-026-06600-w
Anh The Nguyen, Hong Thi Thu Ta, Anh Thi Hai Dao, Hung Manh Vu, Nghia Duy Ngu, Duong Nhu Tran, Hiroyuki Shimizu, Yorihiro Nishimura, Thi Nguyen Hoa-Tran
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引用次数: 0
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