首页|期刊导航|中国兽医杂志|基于遗传演化和密码子分析探究猪伪狂犬病病毒gD基因流行与变异特点

基于遗传演化和密码子分析探究猪伪狂犬病病毒gD基因流行与变异特点OA

Investigation on the Epidemiological and Variation Characteristics of the gD Gene in Porcine Pseudorabies Virus Based on Genetic Evolution and Codon Usage Analysis

中文摘要英文摘要

为了解我国猪伪狂犬病病毒(PRV)的流行现状和变异情况,本试验对获取的150条我国猪源PRV gD全基因组序列进行比对和修剪,并进行系统发育分析、基因流分析、基因选择压力分析、序列遗传距离分析和密码子分析.结果显示,PRV基于gD基因序列分为基因Ⅰ型和Ⅱ型,目前我国流行的PRV毒株以基因Ⅱ型变异毒株2.2亚型为主.基因Ⅰ型和Ⅱ型种群间遗传分化系数均为0.510 38,基因流指标均为0.24.基因Ⅰ型的非同义替换率和同义替换率比值(dN/dS)为1.67(0.010/0.006),基因型2.1和2.2的dN/dS分别为0.33(0.001/0.003)和1.00(0.001/0.001).基因型内遗传距离较低,其中基因型2.2最小(核苷酸遗传距离为0.001,氨基酸遗传距离为0.003);组间核苷酸遗传距离以基因Ⅰ型与基因型2.1之间最大,为0.012;基因型2.1与2.2间核苷酸遗传距离最小,为0.004.3个基因型(Ⅰ型、2.1型、2.2型)的有效密码子数量(ENC)相近,分别为31.03、31.28、31.25.共发现28个高频密码子,均以G或C碱基结尾.3个基因型在ENC-plot中均位于标准曲线的下方.基因Ⅰ型密码子使用偏好性强(相关系数=1.000),基因型2.2偏好性极弱(相关系数=0.004).结果表明,我国PRV gD毒株流行以基因Ⅱ型为主,种群间遗传分化显著,其演化主要受中性突变和随机因素影响,GC含量较高且密码子使用偏好受突变压力主导.本试验结果可为我国PRV防控提供参考依据.

To understand the current epidemic status and variation characteristics of porcine pseudorabies virus(PRV)in China,150 full-length gD gene sequences of swine-derived PRV from China were aligned and trimmed,followed by phylogenetic analysis,gene flow analysis,selection pressure analysis,genetic distance analysis,and codon usage analysis.The results showed that PRV could be divided into genotypes Ⅰ and Ⅱ based on the gD gene sequence,and the currently prevalent PRV strains in China were predominantly genotype Ⅱ variant strains of subtype 2.2.The coefficient of genetic differentiation between genotype Ⅰ and genotype Ⅱ populations was 0.510 38,and the gene flow index was 0.24 for both.The ratio of nonsynonymous to synonymous substitution rates(dN/dS)was 1.67(0.010/0.006)for genotype Ⅰ,and 0.33(0.001/0.003)and 1.00(0.001/0.001)for subtypes 2.1 and 2.2,respectively.Genetic distances within genotypes were low,with genotype 2.2 showing the smallest values(0.001 for nucleotide genetic distance and 0.003 for amino acid genetic distance).Among groups,the largest nucleotide genetic distance was observed between genotype Ⅰ and subtype 2.1(0.012),whereas the smallest was between subtypes 2.1 and 2.2(0.004).The effective number of codons(ENC)was similar among the three genotypes/subtypes(genotype Ⅰ,subtype 2.1,and subtype 2.2),being 31.03,31.28,and 31.25,respectively.A total of 28 high-frequency codons were identified,all ending with G or C.In the ENC-plot,three genotypes/subtypes were located below the standard curve.Genotype Ⅰ showed a strong codon usage bias(correlation coefficient=1.000),whereas subtype 2.2 showed an extremely weak bias(correlation coefficient=0.004).These results indicate that PRV strains circulating in China are predominantly genotype Ⅱ,with significant genetic differentiation among populations.Their evolution is mainly influenced by neutral mutations and random factors,with high GC content and codon usage bias predominantly driven by mutational pressure.These findings provide a reference for the prevention and control of PRV in China.

方双双;李晓冰;陈洪博;谢静蕊;陈志安;陈美椿;何敏嘉;翁成桢;黄欣欣;曹翀;邱龙新

龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000||福建农林大学动物科学学院,福建 福州 350002龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000||福建农林大学动物科学学院,福建 福州 350002龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000||福建农林大学动物科学学院,福建 福州 350002龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000||福建农林大学动物科学学院,福建 福州 350002龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000龙岩学院生命科学学院,福建 龙岩 364000||福建省预防兽医学与兽医生物技术重点实验室,福建 龙岩 364000

农业科技

猪伪狂犬病病毒(PRV)gD基因遗传演化密码子分析

porcine pseudorabies virus(PRV)gD genegenetic evolutioncodon analysis

《中国兽医杂志》 2026 (9)

78-85,8

福建省自然科学基金(2024J01863)福建省中青年教师教育科研重点项目(JZ230057)

10.20157/j.cnki.zgsyzz.2026.sf.022

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