首页|重庆柑橘产区柑橘褪绿矮缩病毒的发生、分布和分子特性研究

重庆柑橘产区柑橘褪绿矮缩病毒的发生、分布和分子特性研究

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【目的】明确柑橘褪绿矮缩病(Citrus chlorotic dwarf-associated virus, CCDaV)在重庆柑橘产区的发生、分布和分子特性,为制定有效防治措施提供理论基础。【方法】对采自重庆的361份疑似感染褪绿矮缩病的柚类和柠檬样品进行CCDaV检测鉴定,通过背靠背引物扩增获得CCDaV的全序列,进而分别使用RDP4和SDTv.1.2进行重组和相似性分析,并采用邻接法构建系统发育树。【结果】在3份红宝石柚(Citrus paradisi)样品中检测出了CCDaV,其全长分别为3642、3640和3641 bp。全基因组分析未发现重组事件,且上述3个CCDaV毒株与已知41个CCDaV毒株的核苷酸和氨基酸相似性分别为99.1%~99.7%和97.3%~99.7%。系统进化树分析显示,本研究中CCDaV毒株被分为了4个不同的类群,其中巫溪样品WX-4-6和WX-4-9,与广东沙田柚上的CCDaV毒株聚在一簇;而巫溪样品WX-2-5与中国柚类上获得的CCDaV毒株聚于另一个分支。【结论】在重庆首次发现了CCDaV,可能是随带病苗木进入。
Occurrence, distribution and molecular characteristics of Citrus chlorotic dwarf-associated virus in Chongqing
【Objective】In 2015, an emerging citrus viral disease caused by Citrus chlorotic dwarf-asso-ciated virus (CCDaV) was first reported in Yunnan province of China, followed by Guangxi and Guang-dong provinces. The present study was undertaken to provide further insight into the distribution of CCDaV in Chongqing municipality, and get a more complete overview of the molecular variability of CCDaV.【Methods】The field survey and collection of samples were conducted from January 2020 to December 2021 in 8 counties of Chongqing municipality, including Beibei, Wanzhou, Jiangjin, etc. A to-tal of 361 suspected CCDaV-infected pummelo and lemon samples were collected from 27 orchards. The samples were randomly evaluated both on normal appearance and on virus-like symptoms of a V-shaped notch and chlorotic freckling on leaves. During sampling, the symptoms on leaves were careful-ly observed. Total DNA extracts were obtained from each plant with DNA extraction kit and used for PCR detection with specific CCDaV primers (sense:5’-GAGCATGTTGAGTGTGAGG-3’and anti-sense (5’- CAGACATAT CCATCAGCGC-3’), which were based on the conserved region of move-ment protein of CCDaV (Genbank accession No. JQ920490). For cloning, three CCDaV-positive sam-ples were selected. The complete genome of CCDaV was amplified by using one pair of primers(3202F:5’-GTTCTGTGTTTCGACCCGTTTCTTGCACTGG-3’and 3202R (5’-CCCCGGTTCTTC-GACCTCCTCTCCGTA-3’), designed based on the CCDaV genome (No. JQ920490), as previously de-scribed. PCR amplified matters were purified with EasyPure quick gel Extraction kit and cloned into pCE2 TA/Blunt-Zero vector. Twelve randomly selected positive clones were custom sequenced. The ge-nomic sequences were assembled by using SeqMan software and submitted to GenBank under accession numbers ON063221-ON063223. Multiple nucleotide sequence alignments of the complete genome of the 3 CCDaV isolates from this study, and 41 CCDaV isolates available in GenBank were conducted sep-arately with Megalign, and the sequence identities were calculated using SDTv.1.2. MEGA 11 was used to construct neighbor-joining phylogenetic trees with 1000 bootstrap replicates. Furthermore, complete genomes of the 44 CCDaV isolates were used for recombination analysis, which was performed with the RDP v4.97 software package.【Results】CCDaV was detected from 0.83%of the collected samples in Chongqing municipality (3 samples were positive out of the 361 samples surveyed) and all of them were originated from Ruby Green pomelo (Citrus grandis) in Wuxi. CCDaV was not found on other pomelo or lemon species. The results showed that CCDaV was not widely distributed in Chongqing municipality. In this study, the young shoots of CCDaV-infected Ruby Green pomelo showed severe leaf twist, shrink and yellowing symptoms. Mild inverted cupping and shrink symptoms were observed on some of Ruby Green pomelo plants, in which CCDaV was not detected, but no variegation symptoms were found in CCDaV-negative plants. The complete genomes of the WX-2-5 had the lengths of 3642 nucleotides (nt) and the base composition was 27.6%A, 16.8%C, 27.3%G and 28.4%T. The complete genomes of the WX-4-6 had the lengths of 3640 nt and the base composition was 27.6%A, 16.7% C, 27.5% G and 28.3%T. The complete genomes of the WX-4-9 had the lengths of 3641 nt and the base composition was 27.6%A, 16.7% C, 27.4% G and 28.3% T. The 5’and 3’untranslated regions (UTRs) of the three CCDaV isolates were 194 nt and 220 nt, respectively. The genome organization of all these CCDaV iso-lates was consistent with that published before. Compared with the CCDaV isolate WX-4-6, WX-4-9 had additional base (T) at position 1203, and WX-2-5 had two more bases (TT) at 1203 and 1204 nt. The ami-no acid sequence alignment showed that there were 4 point mutations at amino acid sequences between WX-2-5 and 41 known CCDaV isolates at positions 303 (C→L), 304 (I→H), 341 (S→N) and 1163 (F→S). There were 3 same point mutations in the amino acid sequences between WX-4-6 and 41 CCDaV iso-lates at 43 (L→W), 567 (H→R) and 722 (R→C). In addition to the same mutation as WX-4-6, WX-4-9 also had mutations at positions 633 (S→N) and 1137 (R→M). Comparisons of the whole genome se-quences of the 3 CCDaV isolates from this study as well as 41 isolates previously reported from around the world revealed that the sequence identity ranged from 99.1%to 99.7%at nucleotide level and 97.3%to 99.7%at amino acid level, respectively, indicating that there was a very low level of sequence hetero-geneity among CCDaV isolates. No recombination event was found among these 44 CCDaV strains. Phy-logenetic tree analysis showed that these 44 CCDaV isolates belonged to four different groups based on geographical origins and host species. CCDaV isolates from China were phylogenetically distinct from the isolates from Turkey, and the CCDaV isolates from Turkey were clustered together in the same branch. CCDaV isolates from Thailand, except CCDaV isolate Tha 30, were all clustered with Chinese CCDaV isolates from pomelo. CCDaV isolates WX-4-6 and WX-4-9 were clustered together with CCDaV isolates on Shatian pomelo from Guangdong province, and CCDaV isolate WX-2-5 strains were clustered in another branch. CCDaV isolates from China and Thailand were more closely related than those from Turkey.【Conclusion】To our knowledge, this is the first report of CCDaV in Chongqing, and the movement of CCDaV-infected planting materials was probably one of the important routes of CCDaV transmission in Chongqing.

Citrus chlorotic dwarf-associated virusDetectionSequence alignmentsPhylogenetic tree analysis

王甲军、乔兴华、秦阳阳、陈力、周彦

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西南大学柑桔研究所国家柑桔工程技术研究中心,重庆北碚 400712

重庆市万州区植物保护与果树技术推广站,重庆万州 404199

柑橘褪绿矮缩病毒 检测 序列分析 进化树

国家重点研发计划财政部和农业农村部:国家现代农业产业技术体系重庆市自然科学基金

2019YFD1001802CARS-26-05Bcstc2019jcyj-msxmX0557

2022

果树学报
中国农业科学院郑州果树研究所

果树学报

CSTPCDCSCD北大核心
影响因子:1.486
ISSN:1009-9980
年,卷(期):2022.39(10)
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