[1]杨宣叶,高明阳,胡欣妍,等.BVDV-2d毒株的分离鉴定及同义密码子使用模式分析[J].江苏农业学报,2024,(11):2111-2121.[doi:doi:10.3969/j.issn.1000-4440.2024.11.015]
 YANG Xuanye,GAO Mingyang,HU Xinyan,et al.Isolation, identification and analysis of synonymous codon usage patterns of BVDV-2d strain[J].,2024,(11):2111-2121.[doi:doi:10.3969/j.issn.1000-4440.2024.11.015]
点击复制

BVDV-2d毒株的分离鉴定及同义密码子使用模式分析()
分享到:

江苏农业学报[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2024年11期
页码:
2111-2121
栏目:
畜牧兽医·水产养殖·益虫饲养
出版日期:
2024-11-30

文章信息/Info

Title:
Isolation, identification and analysis of synonymous codon usage patterns of BVDV-2d strain
作者:
杨宣叶12高明阳12胡欣妍12王进千12王慧慧13丁玉林4曹小安3马晓霞12
(1.西北民族大学生物医学研究中心/生物工程与技术国家民委重点实验室,甘肃兰州730030;2.西北民族大学生命科学与工程学院,甘肃兰州730010;3.中国农业科学院兰州兽医研究所动物疫病防控全国重点实验室,甘肃兰州730046;4.内蒙古农业大学兽医学院动物疾病临床诊疗技术重点实验室,内蒙古呼和浩特010018)
Author(s):
YANG Xuanye12GAO Mingyang12HU Xinyan12WANG Jinqian12WANG Huihui13DING Yulin4CAO Xiaoan3MA Xiaoxia12
(1.Biomedical Research Center/Key Laboratory of Biotechnology and Bioengineering of State Ethnic Affairs Commission, Northwest Minzu University, Lanzhou 730030, China;2.School of Life Sciences and Engineering, Northwest Minzu University, Lanzhou 730010, China;3.State Key Laboratory for Animal Disease Control and Prevention, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China;4.Key Laboratory of Clinical Diagnosis and Treatment Technology in Animal Disease, College of Veterinary Medicine, Inner Mongolia Agricultural University, Hohhot 010018, China)
关键词:
牛病毒性腹泻病毒BVDV-2d病理变化同义密码子遗传
Keywords:
bovine viral diarrhea virusBVDV-2dpathological changesynonymous codonheredity
分类号:
S852.65
DOI:
doi:10.3969/j.issn.1000-4440.2024.11.015
文献标志码:
A
摘要:
本研究通过对腹泻犊牛肠道内容物中分离到的牛病毒性腹泻病毒(BVDV)毒株进行分析,首次确认该毒株为BVDV-2d亚型,命名为22-Gansu-F3。通过病毒分离、鉴定及全基因组测序,本研究不仅探讨了腹泻犊牛肠道的病理变化,还分析了其同义密码子使用模式的遗传特征。结果表明,在开放阅读框中,CpG二核苷酸的使用频率显著降低,并且在选择同义密码子的过程中,精氨酸对含CpG同义密码子的使用具有显著抑制作用。为了进一步明确不同功能性蛋白质编码序列的同义密码子使用模式的遗传学特征,本研究比较了不同编码序列的同义密码子使用差异,发现Npro和NS4A的编码区在同义密码子使用上与其他蛋白质显著不同。此外,BVDV-2d型22-Gansu-F3毒株的不同蛋白质编码区在适应猪、羊和骆驼的同义密码子使用模式上表现出良好的适应性,为这些动物体内病毒蛋白的翻译提供了潜在的物质基础。本研究结果为中国BVDV-2型的进化动态提供了新的理论依据,并为预防该亚型成为中国主要流行亚型提供了早期预警。
Abstract:
This study analyzed a bovine viral diarrhea virus (BVDV) strain isolated from the intestinal contents of diarrheic calves, and classified it as subtype BVDV-2d for the first time and designated it as 22-Gansu-F3. Through viral isolation, identification, and whole-genome sequencing, this study not only explored the pathological changes in the intestines of diarrheic calves, but also analyzed the genetic characteristics of their synonymous codon usage pattern. Our findings revealed a significant reduction in the usage frequency of CpG dinucleotides within open reading frames. Besides, arginine showed notable suppression of synonymous codon usage containing CpG during the selection process for synonymous codon. To elucidate the genetic features of synonymous codon usage patterns among various functional protein-coding sequences, we compared the usage differences of synonymous codons in different coding sequences and found significant differences in the synonymous codon usage of the Npro and NS4A encoding regions compared to other proteins. Furthermore, the different protein-coding regions of the BVDV-2d strain 22-Gansu-F3 exhibited good adaptability for synonymous codon usage pattern in pigs, sheep, and camels, and provided a potential material basis for the translation of viral proteins in these hosts. The research results offer new theoretical insights into the evolutionary dynamics of BVDV subtype 2 in China and serve as an early warning to prevent this subtype from becoming the predominant circulating subtype.

参考文献/References:

[1]RIDPATH J F. BVDV genotypes and biotypes: practical implications for diagnosis and control[J]. Biologicals:Journal of the International Association of Biological Standardization,2003,31(2):127-131.
[2]LANYON S R, HILL F I, REICHEL M P, et al. Bovine viral diarrhoea:pathogenesis and diagnosis[J]. Veterinary Journal,2014,199(2):201-209.
[3]ZHOU J H, GAO Z L, ZHANG J, et al. Comparative the codon usage between the three main viruses in pestivirus genus and their natural susceptible livestock[J]. Virus Genes,2012,44(3):475-481.
[4]DENG R, BROCK K V. Molecular cloning and nucleotide sequence of a pestivirus genome, noncytopathic bovine viral diarrhea virus strain SD-1[J]. Virology,1992,191(2):867-869.
[5]BAUERMANN F V, RIDPATH J F. HoBi-like viruses-the typical ‘atypical bovine pestivirus’[J]. Animal Health Research Reviews,2015,16(1):64-69.
[6]DENG M L, JI S K, FEI W T, et al. Prevalence study and genetic typing of bovine viral diarrhea virus (BVDV) in four bovine species in China[J]. PLoS One,2015,10(4):e0121718.
[7]WANG H H, WANG M Z, FENG X L, et al. Genetic features of bovine viral diarrhea virus subgenotype 1c in newborn calves at nucleotide and synonymous codon usages[J]. Frontiers in Veterinary Science,2022,9:984962.
[8]ZHANG K, ZHANG J Y, QIU Z Y, et al. Prevalence characteristic of BVDV in some large scale dairy farms in Western China[J]. Frontiers in Veterinary Science,2022,9:961337.
[9]ZHU J, WANG C, ZHANG L N, et al. Isolation of BVDV-1a, 1m, and 1v strains from diarrheal calf in china and identification of its genome sequence and cattle virulence[J]. Frontiers in Veterinary Science,2022,9:1008107.
[10]YARNALL M J, THRUSFIELD M V. Engaging veterinarians and farmers in eradicating bovine viral diarrhoea:a systematic review of economic impact[J]. The Veterinary Record,2017,181(13):347.
[11]EVANS C A, PINIOR B, LARSKA M, et al. Global knowledge gaps in the prevention and control of bovine viral diarrhoea (BVD) virus[J]. Transboundary and Emerging Diseases,2019,66(2):640-652.
[12]MA X X, MA P, CHANG Q Y, et al. The analyses of relationships among nucleotide, synonymous codon and amino acid usages for E2 gene of bovine viral diarrhea virus[J]. Gene,2018,660:62-67.
[13]WANG L N, WU X M, WANG C B, et al. Origin and transmission of bovine viral diarrhea virus type 1 in China revealed by phylodynamic analysis[J]. Research in Veterinary Science,2020,128:162-169.
[14]ZHOU Y, REN Y, DAI G, et al. Genetic characterization and clinical characteristics of bovine viral diarrhea viruses in cattle herds of Heilongjiang province, China[J]. Iranian Journal of Veterinary Research,2022,23(1):69-73.
[15]CHANG L L, QI Y P, LIU D, et al. Molecular detection and genotyping of bovine viral diarrhea virus in Western China[J]. BMC Veterinary Research,2021,17(1):66.
[16]GAO M Y, YANG X Y, WU Y H, et al. Analysis for codon usage bias in membrane anchor of nonstructural protein 5A from BVDV[J]. Journal of Basic Microbiology,2023,63(10):1106-1114.
[17]MUCELLINI C I, SILVA JU'NIOR J V J, DE OLIVEIRA P S B, et al. Novel genomic targets for proper subtyping of bovine viral diarrhea virus 1 (BVDV-1) and BVDV-2[J]. Virus Genes,2023,59(6):836-844.
[18]MUHSEN M, AOKI H, IKEDA H, et al. Biological properties of bovine viral diarrhea virus quasispecies detected in the RK13 cell line[J]. Archives of Virology,2013,158(4):753-763.
[19]SHARP P M, LI W H. Codon usage in regulatory genes in Escherichia coli does not reflect selection for rare codons[J]. Nucleic Acids Research,1986,14(19):7737-7749.
[20]GUSTAFSSON C, GOVINDARAJAN S, MINSHULL J. Codon bias and heterologous protein expression[J]. Trends in Biotechnology,2004,22(7):346-353.
[21]WRIGHT F. The ‘effective number of codons’ used in a gene[J]. Gene,1990,87(1):23-29.
[22]ZHOU J H, ZHANG J Z, SUN D J, et al. The distribution of synonymous codon choice in the translation initiation region of dengue virus[J]. PLoS One,2013,8(10):e77239.
[23]NAKAMURA Y, GOJOBORI T, IKEMURA T. Codon usage tabulated from international DNA sequence databases:status for the year 2000[J]. Nucleic Acids Research,2000,28(1):292.
[24]DIAO N C, GONG Q L, LI J M, et al. Prevalence of bovine viral diarrhea virus (BVDV) in yaks between 1987 and 2019 in mainland China:a systematic review and meta-analysis[J]. Microbial Pathogenesis,2020,144:104185.
[25]SHAH P T, NAWAL BAHOUSSI A, AHMAD A, et al. Bovine viral diarrhea virus in China:a comparative genomic and phylogenetic analysis with complete genome sequences[J]. Frontiers in Veterinary Science,2022,9:992678.
[26]YESILBAG K, ALPAY G, BECHER P. Variability and global distribution of subgenotypes of bovine viral diarrhea virus[J]. Viruses,2017,9(6):128.
[27]WANG W, SHI X C, CHEN C Y, et al. Genetic characterization of a noncytopathic bovine viral diarrhea virus 2b isolated from cattle in China[J]. Virus Genes,2014,49(2):339-341.
[28]ZHANG S Q, TAN B, DING Y L, et al. Complete genome sequence and pathogenesis of bovine viral diarrhea virus JL-1 isolate from cattle in China[J]. Virology Journal,2014,11:67.
[29]BIANCHI M V, KONRADT G, DE SOUZA S O, et al. Natural outbreak of BVDV-1d-induced mucosal disease lacking intestinal lesions[J]. Veterinary Pathology,2017,54(2):242-248.
[30]KELLING C L, STEFFEN D J, COOPER V L, et al. Effect of infection with bovine viral diarrhea virus alone, bovine rotavirus alone, or concurrent infection with both on enteric disease in gnotobiotic neonatal calves[J]. American Journal of Veterinary Research,2002,63(8):1179-1186.
[31]KOONIN E V, DOLJA V V, KRUPOVIC M. The logic of virus evolution[J]. Cell Host & Microbe,2022,30(7):917-929.
[32]SANJUN R, DOMINGO-CALAP P. Mechanisms of viral mutation[J]. Cellular and Molecular Life Sciences,2016,73(23):4433-4448.
[33]LIU C, LIU Y H, LIANG L, et al. RNA-Seq based transcriptome analysis during bovine viral diarrhoea virus (BVDV) infection[J]. BMC Genomics,2019,20(1):774.
[34]ATKINSON N J, WITTEVELDT J, EVANS D J, et al. The influence of CpG and UpA dinucleotide frequencies on RNA virus replication and characterization of the innate cellular pathways underlying virus attenuation and enhanced replication[J]. Nucleic Acids Research,2014,42(7):4527-4545.
[35]FROS J J, DIETRICH I, ALSHAIKHAHMED K, et al. CpG and UpA dinucleotides in both coding and non-coding regions of echovirus 7 inhibit replication initiation post-entry[J]. eLife,2017,6:e29112.
[36]MAGNUSSON M, MAGNUSSON S, VALLIN H, et al. Importance of CpG dinucleotides in activation of natural IFN-alpha-producing cells by a lupus-related oligodeoxynucleotide[J]. Scandinavian Journal of Immunology,2001,54(6):543-550.
[37]UCCELLINI M B, BUSCONI L, GREEN N M, et al. Autoreactive B cells discriminate CpG-rich and CpG-poor DNA and this response is modulated by IFN-alpha[J]. Journal of Immunology,2008,181(9):5875-5884.
[38]CHI S S, CHEN S, JIA W J, et al. Non-structural proteins of bovine viral diarrhea virus[J]. Virus Genes,2022,58(6):491-500.
[39]TAO J, LIAO J H, WANG J Y, et al. Pig BVDV-2 non-structural protein (Npro) links to cellular antiviral response in vitro[J]. Virus Genes,2017,53(2):233-239.
[40]FELLENBERG J, DUBRAU D, ISKEN O, et al. Packaging defects in pestiviral NS4A can be compensated by mutations in NS2 and NS3[J]. Journal of Virology,2023,97(9):e0057223.
[41]ZHOU M, GUO J H, CHA J, et al. Non-optimal codon usage affects expression, structure and function of clock protein FRQ[J]. Nature,2013,495(7439):111-115.
[42]OESTRINGER B P, BOLIVAR J H, CLARIDGE J K, et al. Hepatitis C virus sequence divergence preserves p7 viroporin structural and dynamic features[J]. Scientific Reports,2019,9(1):8383.
[43]XU X R, ZHANG Q C, YU X L, et al. Sequencing and comparative analysis of a pig bovine viral diarrhea virus genome[J]. Virus Research,2006,122(1/2):164-170.
[44]TAO J, WANG Y, WANG J, et al. Identification and genetic characterization of new bovine viral diarrhea virus genotype 2 strains in pigs isolated in China[J]. Virus Genes,2013,46(1):81-87.
[45]GAO S D, LUO J H, DU J Z, et al. Serological and molecular evidence for natural infection of Bactrian camels with multiple subgenotypes of bovine viral diarrhea virus in Western China[J]. Veterinary Microbiology,2013,163(1/2):172-176.
[46]QI S H, WO L J, SUN C, et al. Host cell receptors implicated in the cellular tropism of BVDV[J]. Viruses,2022,14(10):2302.
[47]GRANT D M, DAGLEISH M P, BACHOFEN C, et al. Assessment of the rabbit as a wildlife reservoir of bovine viral diarrhea virus:serological analysis and generation of trans-placentally infected offspring[J]. Frontiers in Microbiology,2015,6:1000.
[48]LIU Y, WU C H, CHEN N N, et al. PD-1 Blockade restores the proliferation of peripheral blood lymphocyte and inhibits lymphocyte apoptosis in a balb/c mouse model of CP BVDV acute infection[J]. Frontiers in Immunology,2021,12:727254.
[49]CHEN N N, JIANG D J, SHAO B H, et al. Anti-BVDV activity of traditional chinese medicine monomers targeting NS5B (RNA-dependent RNA polymerase) in vitro and in vivo[J]. Molecules,2023,28(8):3413.

相似文献/References:

[1]常秋燕,郭富城,冶昡青,等.牛病毒性腹泻病毒Npro蛋白的原核表达及裂解效率[J].江苏农业学报,2019,(05):1161.[doi:doi:10.3969/j.issn.1000-4440.2019.05.023]
 CHANG Qiu-yan,GUO Fu-cheng,YE Xuan-qing,et al.Prokaryotic expression and splitting decomposition rate of N pro protein of bovine viral diarrhea virus[J].,2019,(11):1161.[doi:doi:10.3969/j.issn.1000-4440.2019.05.023]

备注/Memo

备注/Memo:
收稿日期:2024-04-06基金项目:甘肃省自然科学基金项目(23JRRA715)作者简介:杨宣叶(2001-),男,河南周口人,硕士研究生,主要从事病毒基因工程研究。(E-mail)yangxuanye2001@163.com通讯作者:马晓霞,(E-mail)maxiaoxia956@163.com
更新日期/Last Update: 2025-01-20