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Natural infection of purple passion fruit (Passiflora edulis f. edulis) by a novel member of the family Tymoviridae in Colombia. 哥伦比亚Tymoviridae科新成员对紫百香果(Passiflora edulis f. edulis)的自然感染。
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_310
Daniela Cardona, Andrea Restrepo, Mónica Higuita, Yuliana Gallo, Mauricio Marin, Pablo Gutiérrez

Purple passion fruit is one of the most important fruit exports of Colombia, but its productivity is being compromised by the emergence of several viral diseases. High-throughput sequencing (HTS) surveys of viruses in purple passion fruit fields in the province of Antioquia suggested infection by a new member of the family Tymoviridae. In this work, we characterize the complete genome sequence of this virus, tentatively named purple passionfruit leaf deformation virus (PpLDV), and evaluate its distribution in Antioquia. PpLDV was assembled at high coverage in four datasets from different regions. The 6.1 kb genome of PpLDV encodes a single polyprotein with domains characteristic of the family Tymoviridae, contains a marafibox-like promoter and the 3'-UTR can fold into a tRNA-like secondary structure with a valine anti-codon. Phylogenetic analysis of the polyprotein revealed that PpLDV is a distinct member of the family Tymoviridae, more closely related to the genus Tymovirus and the unclassified Poinsettia mosaic virus (PnMV). The presence of PpLDV was confirmed by RT-qPCR and RT-PCR in samples from commercial purple passion fruit fields, plantlets and seed sprouts collected in Antioquia using primers designed in this study. Keywords: high-throughput sequencing; Marafivirus; Passifloraceae; plant virology; RT-qPCR; Tymovirus.

紫百香果是哥伦比亚最重要的出口水果之一,但其产量因几种病毒性疾病的出现而受到影响。对安蒂奥基亚省紫百香果田病毒的高通量测序(HTS)调查表明,该病毒感染了Tymoviridae科的一种新成员。在这项工作中,我们鉴定了这种病毒的全基因组序列,暂时命名为紫色西番莲叶片变形病毒(PpLDV),并评估了它在安蒂奥基亚的分布。PpLDV在来自不同区域的4个数据集中进行高覆盖组装。PpLDV的6.1 kb基因组编码一个具有Tymoviridae家族特征结构域的单一多蛋白,包含一个marafibox样启动子,并且3'-UTR可以折叠成具有缬氨酸抗密码子的trna样二级结构。该多蛋白的系统发育分析表明,PpLDV是Tymoviridae科的一个独特成员,与Tymovirus属和未分类的一品红花叶病毒(PnMV)关系更密切。利用本研究设计的引物,对安蒂奥基亚省商业紫百香果田、植株和种子芽样品进行RT-qPCR和RT-PCR检测,证实了PpLDV的存在。关键词:高通量测序;Marafivirus;西番莲;植物病毒学;RT-qPCR;Tymovirus。
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引用次数: 0
An integrated view of protein homologue groups and functional genomic development of baculoviruses: towards understanding baculoviral infection mechanism and improving baculoviral expression vector 杆状病毒蛋白同源群和功能基因组发育的综合研究:对杆状病毒感染机制的理解和杆状病毒表达载体的改进
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_405
Weiping Lin, Yanhua Shi, T. Yu, Yujiao Wang, Yonglin Tan, Punan Zhao, Guohui Wang, Dianhai Hou
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引用次数: 0
Identification of dicistro-like viruses in the transcriptome data of Striga asiatica and other plants. 亚洲曲带及其他植物转录组数据中双盘状病毒的鉴定。
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_205
Chaerim Shin, Dongjin Choi, Ken Shirasu, Yoonsoo Hahn

Dicistroviruses (the family Dicistroviridae) are positive-sense single-stranded RNA viruses of the order Picornavirales, which is a rapidly growing viral group. They have been detected in a wide range of animals, predominantly in insects and crustaceans. In this study, we identified the genome sequences of 14 dicistro-like viruses in the transcriptome data from 12 plant species, including Striga asiatica dicistro-like virus 1 and 2 identified in the transcriptome data of Striga asiatica. Sequence comparison and phylogenetic analysis indicated that these 14 plant-associated dicistro-like viruses were novel members of the family Dicistroviridae, five of which are placed within the genera Aparavirus and Cripavirus, which mainly consist of viruses infecting animals, including insects. The other nine plant dicistro-like viruses formed clades with unclassified dicistroviruses. Our study implies that a wide range of plant species may serve as hosts for dicistroviruses or reservoirs for their transmission. Keywords: dicistrovirus; Dicistroviridae; plant; transcriptome; Striga asiatica.

双股病毒(双股病毒科)是小核糖核酸目的正义单链RNA病毒,是一个快速增长的病毒群。它们已在许多动物中被检测到,主要是昆虫和甲壳类动物。在本研究中,我们从12种植物的转录组数据中鉴定了14个双盘状病毒的基因组序列,其中包括在亚洲striiga dicisto -like病毒1和2中鉴定的亚洲striiga dicisto -like病毒。序列比较和系统发育分析表明,这14种植物相关的dicistro样病毒是Dicistroviridae科的新成员,其中5种属于Aparavirus和cripavvirus属,主要由感染动物(包括昆虫)的病毒组成。其他九种植物类二歧病毒与未分类的二歧病毒形成分支。我们的研究表明,广泛的植物物种可以作为二叉病毒的宿主或其传播的宿主。关键词:dicistrovirus;Dicistroviridae;植物;转录组;Striga asiatica。
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引用次数: 5
Development of RT-PCR for rapid detection of ssRNA ambi-like mycovirus in a root rot fungi (Armillaria spp.). 快速检测根腐菌(蜜环菌)ssRNA双歧样分枝病毒的RT-PCR方法的建立。
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_308
Tomáš Tonka, Lucie Walterová, Vladislav Čurn

Letter to the editor (No abstract) Keywords.

给编辑的信(无摘要)
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引用次数: 0
Dwarf polish wheat hosts a novel closterovirus: Revelation by transcriptome data-mining. 矮波兰小麦宿主一种新的clostervirus:通过转录组数据挖掘的启示。
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_207
Venkidusamy Kavi Sidharthan, Virendra Kumar Baranwal

losteroviruses are positive sense single-stranded RNA genome-containing plant viruses with narrow natural host range and wide distribution. In the present study, a putative novel closterovirus, Triticum polonicum closterovirus (TriPCV) was identified in the transcriptome assembled contigs of dwarf polish wheat available in public domain. The genome of TriPCV (15.36 kb; TPA Acc. No.: BK059767) contained nine open reading frames (ORFs) that encode for proteins involved in viral replication, cell-to-cell movement, encapsidation and suppression of host RNA silencing. Phylogenetic analysis revealed that TriPCV was distantly related to other members of the genus Closterovirus. Based on genome organization, sequence similarities in BLAST analysis, predicted motifs and phylogeny, TriPCV can be regarded as a putative novel member of the genus Closterovirus Keywords: Closterovirus; Triticum polonicum; transcriptome; public domain.

失落病毒是一种天然宿主范围窄、分布广泛的植物正义单链RNA基因组病毒。在本研究中,在公共领域的矮波兰小麦转录组组装组中发现了一种假定的新型clostervirus,即波兰小麦clostervirus (TriPCV)。TriPCV的基因组(15.36 kb;TPA Acc。不。编号:BK059767)含有9个开放阅读框(orf),编码参与病毒复制、细胞间运动、衣壳化和抑制宿主RNA沉默的蛋白质。系统发育分析表明,TriPCV与其他clostervirus属成员有远亲关系。基于基因组组织、BLAST分析序列相似性、预测基序和系统发育,TriPCV可以被认为是clostervirus属的一个假定的新成员;波兰小麦;转录组;公共领域。
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引用次数: 1
Evaluation of the effects of 1,25VitD3 on Th17 cells and Tregs in HTLV-1 infected cell lines. 1,25维生素d3对HTLV-1感染细胞系中Th17细胞和Tregs的影响
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_202
Qing Huang, Zhijie Ling, Huabin Wang, Xiaoming Zhong, Kaiyuan Luo

Human T-lymphotropic virus type 1 (HTLV-1) causes chronic infections of human T lymphocytes. The present study aimed to evaluate the effects of 1,25VitD3 on the proportion of Tregs and Th17 cells, the expression of related transcription factors (ROR-γt and FOXP3) and cytokines (IL-10, TGF-β, IL-6, and IL-17 A) in the HTLV-1infected cell lines MT-2 and MT-4. MT-2 and MT-4 cells and control PBMCs were treated with 1,25VitD3 and percentages of Tregs and Th17 cells was determined by flow cytometry. Gene expression and cytokine levels were analyzed by real-time PCR and ELISA, respectively. Treatment with-1,25VitD3 increased the percentage of Tregs in MT-2 and MT-4 cells, while it decreased the percentage of Th17 cells among MT-2 cells. 1,25VitD3 treatment also significantly improved FOXP3 gene expression in MT-2 cells, while reducing ROR-γt-gene expression in MT-2 and MT-4 cells comparing to untreated cells. Treatment with 1,25VitD3 significantly improved IL-10 levels in MT-2 cells, as well as TGF-β levels in both cell lines culture supernatants. 1,25VitD3 treatment diminished IL-6 levels in cell culture supernatants of MT-2 and MT-4 as well as IL-17 A levels in MT-2. Here we showed, that 1,25VitD3 modulated immune responses by enhancing Tregs differentiation and functions as well as inhibiting Th17 differentiation and actions in HTLV-1 infected cell lines. This suggests that VitD3 may have therapeutic effects in HTLV-1-related diseases by suppressing adverse inflammatory responses. Keywords: Tregs; Th17 cells; HTLV-1; 1, 25VitD3.

人类嗜T淋巴病毒1型(HTLV-1)引起人类T淋巴细胞的慢性感染。本研究旨在评价1,25 vitd3对htlv -1感染细胞系MT-2和MT-4中Tregs和Th17细胞比例、相关转录因子(ROR-γt和FOXP3)和细胞因子(IL-10、TGF-β、IL-6和IL-17 A)表达的影响。用1,25 vitd3处理MT-2和MT-4细胞及对照PBMCs,流式细胞术检测Tregs和Th17细胞的百分比。采用实时荧光定量PCR和酶联免疫吸附法分析基因表达和细胞因子水平。-1,25 vitd3增加了MT-2和MT-4细胞中Tregs的百分比,而降低了MT-2细胞中Th17细胞的百分比。1,25 vitd3处理也显著提高MT-2细胞中FOXP3基因的表达,同时与未处理的细胞相比,降低MT-2和MT-4细胞中ROR-γt基因的表达。1,25 vitd3处理显著提高MT-2细胞中IL-10水平,以及两种细胞系培养上清中TGF-β水平。1,25 vitd3处理降低MT-2和MT-4细胞培养上清液中的IL-6水平以及MT-2中的IL-17 A水平。在HTLV-1感染细胞系中,1,25 vitd3通过增强Tregs的分化和功能以及抑制Th17的分化和作用来调节免疫应答。这表明VitD3可能通过抑制不良炎症反应对htlv -1相关疾病具有治疗作用。关键词:亚群;Th17细胞;htlv 1;1,25 vitd3。
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引用次数: 1
Comparative analysis of HBV basic core promoter/pre-core gene mutations and viral quasispecies diversity in HIV/HBV co-infected and HBV mono-infected patients. HIV/HBV合并感染与HBV单一感染患者HBV基本核心启动子/前核心基因突变及病毒准种多样性的比较分析
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_103
Haohui Deng, Hongbo Gao, Yu Liu, Ying Xu, Juncheng Yang, Miaoxian Zhao, Huiyuan Liu, Zhanhui Wang
Human immunodeficiency virus (HIV)/hepatitis B virus (HBV) co-infection accelerates the progression of HBV-related liver diseases. HBV basic core promoter (BCP)/pre-core (preC) gene mutations may be one of the most important risk factors. In this study, a total of 230 patients were recruited, and 199 patients whose HBV BCP/preC gene were successfully amplified and sequenced, including 99 HIV/HBV co-infected and 100 HBV mono-infected patients. Next-generation sequencing was used for detection of BCP/preC mutations which were then compared in patients with different HBV genotypes and different HBeAg statuses, and 1% and 20% cutoff values were defined to evaluate the mutations. HBV quasispecies diversity was also compared in HIV/HBV co-infected and HBV mono-infected patients. Among the patients infected with HBV genotype C and HBeAg-negative status, the frequency of A1762T/G1764A double mutations was significantly lower in HIV/HBV co-infected patients than in HBV mono-infected patients (53.3% vs. 100.0%, P = 0.008) regardless of the 1% or 20% cutoff value level. However, A1762T/G1764A double mutations did not differ in the other groups (P >0.05). Viral quasispecies diversity was lower in HIV/HBV co-infected patients than in HBV mono-infected patients (P Keywords: human immunodeficiency virus, hepatitis B virus; mutations; viral quasispecies; next-generation sequencing.
人类免疫缺陷病毒(HIV)/乙型肝炎病毒(HBV)联合感染加速了HBV相关肝脏疾病的进展。HBV基本核心启动子(BCP)/前核心(preC)基因突变可能是最重要的危险因素之一。本研究共招募230例患者,成功扩增并测序HBV BCP/preC基因的患者199例,其中HIV/HBV共感染者99例,HBV单感染者100例。采用新一代测序检测BCP/preC突变,比较不同HBV基因型和不同HBeAg状态患者的BCP/preC突变,并定义1%和20%的截止值来评估突变。还比较了HIV/HBV合并感染和HBV单一感染患者的HBV准种多样性。在HBV基因型C和hbeag阴性的患者中,无论是1%还是20%的临界值水平,HIV/HBV合并感染患者的A1762T/G1764A双突变频率均显著低于HBV单感染患者(53.3% vs. 100.0%, P = 0.008)。而A1762T/G1764A双突变在其他组间差异无统计学意义(P < 0.05)。HIV/HBV合并感染患者的病毒准种多样性低于HBV单一感染患者(P);突变;病毒准物种;下一代测序。
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引用次数: 1
A novel approach for estimation of anti-FMDV protective immunity generated in multiple vaccinated field animals. 一种估算多种接种动物抗口蹄疫保护性免疫的新方法。
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_110
B. Jain, Anuj Tewari, M. Prasad, S. K. Kadian
In this study, forty serum samples from field buffaloes vaccinated with inactivated foot-and-mouth disease (FMD) vaccine were collected. These animals were multiple vaccinated with the above vaccine during previous years. The study was conducted to determine the actual status of the protective antibodies generated after vaccination. Initially, the serum samples were tested by Liquid phase blocking ELISA (LPBE), and only samples with titer more than 1.4 in LPBE were chosen for further analysis. These samples were tested with an in-house Gold Nanoparticle-based test for detection of anti-FMDV structural protein antibodies, in which the antibodies were detected at 10-4 dilution; this was suggestive of strong antibody titer generated post-vaccination. To test the binding affinity of these antibodies with the antigen, an avidity ELISA was developed and outcomes were expressed in terms of avidity index (AI). It was found that the avidity was low in some of the animals even after multiple vaccinations. Therefore, multiple vaccinations and strong antibody titer generation may not be the actual indicator of the protective immune response generated. We conclude that avidity ELISA can be a better approach than LPBE to measure the level of protective antibodies generated post-vaccination. Keywords: avidity ELISA; foot-and-mouth disease; post-vaccination monitoring; herd immunity; PCP-FMD.
本研究收集了40份接种口蹄疫灭活疫苗的野地水牛血清样本。这些动物在前几年多次接种上述疫苗。本研究旨在确定疫苗接种后产生的保护性抗体的实际状态。初步采用液相阻断ELISA (Liquid phase blocking ELISA, LPBE)检测血清样本,仅选择LPBE效价大于1.4的样本进行进一步分析。这些样品使用内部基于金纳米颗粒的检测抗fmdv结构蛋白抗体的测试进行测试,其中抗体在10-4稀释下检测;这提示疫苗接种后产生了强抗体滴度。为了测试这些抗体与抗原的结合亲和力,开发了亲和度ELISA,并用亲和度指数(AI)表达结果。结果发现,即使多次接种疫苗,部分动物的贪婪度仍很低。因此,多次接种和强抗体滴度的产生可能不是保护性免疫反应产生的实际指标。我们得出结论,贪婪ELISA可以比LPBE更好地测量疫苗接种后产生的保护性抗体水平。关键词:贪婪酶联免疫吸附试验;手足口病;接种后的监控;群体免疫;PCP-FMD。
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引用次数: 1
RPS3-induced antiviral cytokines inhibit the proliferation of classical swine fever virus. rps3诱导的抗病毒细胞因子抑制猪瘟病毒的增殖。
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2022-01-01 DOI: 10.4149/av_2022_107
Di Zhao, Liang Zhang, Mengzhao Song, Yanming Zhang Mail
Classical swine fever virus (CSFV) infection results in serious economic losses to the pig industry. This positive-sense RNA virus hijacks cell host proteins for its own replication. Although previous studies have shown that RPS3, a 40S ribosomal subunit protein, is mainly required for DNA repair, apoptosis and inflammation, the effect of RPS3 on CSFV replication remains uncertain. Thus, we investigated the potential role of RPS3 in CSFV infection in RPS3-knockdown and -overexpressing cell lines using real-time fluorescence quantitative PCR (RT-qPCR) and indirect immunofluorescence assays. Results showed that knockdown of RPS3 by lentiviruses enhanced CSFV replication, whereas overexpression of RPS3 by lentiviruses inhibited CSFV replication. These findings indicated the antiviral role of RPS3 in CSFV infection. Subsequent experiments revealed that CSFV replication was inhibited in cells cultured with the supernatants of RPS3-overexpressing cell, suggesting that the RPS3-mediated inflammatory response was involved in CSFV infection. Furthermore, enzyme-linked immunosorbent assay (ELISA) revealed that the secretion of antiviral cytokines (IL-8 and INF-β) was increased in cells with sufficient RPS3 expression but decreased in cells lacking RPS3 expression. RT-qPCR and immunofluorescence assays revealed that CSFV infection inhibited RPS3-mediated antiviral cytokine secretion. Taken together, these findings reveal that RPS3 is a novel antiviral factor that inhibits CSFV proliferation by increasing antiviral cytokine secretion. Keywords: classical swine fever virus; ribosome protein S3; IL-8; INF-β.
猪瘟病毒(CSFV)感染给养猪业造成严重的经济损失。这种正义RNA病毒劫持细胞宿主蛋白进行自身复制。虽然已有研究表明RPS3是一种40S核糖体亚基蛋白,主要参与DNA修复、细胞凋亡和炎症反应,但RPS3对猪瘟病毒复制的影响尚不确定。因此,我们利用实时荧光定量PCR (RT-qPCR)和间接免疫荧光法研究了RPS3在猪瘟病毒感染中的潜在作用。结果表明,慢病毒敲低RPS3可增强猪瘟病毒的复制,而过表达RPS3可抑制猪瘟病毒的复制。这些发现提示RPS3在猪瘟感染中的抗病毒作用。随后的实验发现,用rps3过表达细胞的上清液培养的细胞可以抑制猪瘟病毒的复制,这表明rps3介导的炎症反应参与了猪瘟病毒感染。此外,酶联免疫吸附试验(ELISA)显示,抗病毒细胞因子(IL-8和INF-β)在RPS3表达充足的细胞中分泌增加,而在RPS3缺乏表达的细胞中分泌减少。RT-qPCR和免疫荧光检测显示猪瘟病毒感染抑制rps3介导的抗病毒细胞因子分泌。综上所述,这些发现表明RPS3是一种新的抗病毒因子,通过增加抗病毒细胞因子的分泌来抑制猪瘟病毒的增殖。关键词:猪瘟病毒;核糖体蛋白S3;引发;正-β。
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引用次数: 4
Sequencing and phylogenetic characterization of a novel RNA virus in Arma chinensis. 中国犰狳一种新型RNA病毒的测序和系统发育特征。
IF 1.7 4区 医学 Q4 VIROLOGY Pub Date : 2021-01-01 DOI: 10.4149/av_2021_310
Yonghao Dong, Pengjun Xu, Guangwei Ren, Changchun Feng, Dongyang Liu, Lianqiang Jiang, Fangzhao Jia, Changhua Zhang, Qinggang Gao, Yongjie Liu

The complete genome of a novel virus from Arma chinensis was determined by RNA sequencing and rapid amplification of cDNA ends. This virus has a single-stranded RNA genome of 10,540 nucleotides (nt) excluding the poly(A) tail. Two non-overlapping open reading frames (ORFs) in the sense direction were predicted: one long ORF at the 5' end of the genome (6,219 nt) that encodes a polypeptide of 2,072 amino acids (aa), and one short ORF at the 3' end of the genome (3,033 nt) that encodes a polypeptide of 1,010 aa. Phylogenetic analysis indicated that the virus clusters within a large cluster of currently unidentified picorna-like viruses with a high bootstrap value. We named the virus isolate Arma chinensis picorna-like virus 1 (AcPV-1). The prevalence of AcPV-1 infection in samples of Arma chinensis from the wild was at a low level (5.48%, 8 positives in 146 samples). Keywords: Arma chinensis; genomic characterization; phylogenetic analysis; Arma chinensis picorna-like virus 1; prevalence.

采用RNA测序和cDNA末端快速扩增的方法,确定了一种新型中华剑虫病毒的全基因组。该病毒具有单链RNA基因组,包含10,540个核苷酸(nt),不包括聚(a)尾部。在意义方向上预测了两个不重叠的开放阅读框(ORF):一个位于基因组5'端(6,219 nt)的长ORF编码2,072个氨基酸(aa)的多肽,一个位于基因组3'端(3,033 nt)的短ORF编码1,010个氨基酸的多肽。系统发育分析表明,该病毒聚集在一大群目前尚未确定的小核糖核酸样病毒中,具有很高的自举值。我们将该病毒分离物命名为中华袖珍小核糖核酸样病毒1号(AcPV-1)。野生中华armma Arma chinensis AcPV-1感染率较低(5.48%,146份标本中8份呈阳性)。关键词:中华犰狳;基因组特征;系统发育分析;中华袖珍猴类病毒1型;患病率。
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引用次数: 1
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