斜纹夜蛾核多角体病流行的时间动态

通过对病病幼虫进行跟踪观察,观察了病毒不同浓度处理下,斜纹夜蛾核多角体病的田间流行动态结果表明,在试验病毒浓度范围（３．１＊１０＾５－３．１＾１０＾８ＰＩＢｓ．ｍｌ＾－１）内,幼虫大多在喷施病毒后第４天开始发病,第５－７天为发病高峰,第５－６天开始病死,第６－天为病死高峰,宿主现患高峰民发病高峰基本一致。宿主种群发病和病死时间分布可用时间－剂量－死亡率模型较好地拟合,模型模拟与实测值有较好的吻合（     

斜纹夜蛾核多角体病毒几丁质酶基因的克隆及序列分析

以苜蓿丫纹夜蛾核多角体病毒（Ａｕｔｏｇｒａｐｈａ ｃａｌｉｔｉｒｎｉｃａ ｍｕｌｔｉｎｕｃｌｅｏｃａｐｓｉｄ ｎｕｃｌｅａｒ ｐｏｌｙｈｅｄｒｏｓｉｓ ｖｉｒｕｓ,ＡｃＭＮ－ＰＶ）基因组含几丁质酶基因（ｃｈｉＡ）的ｐｓｔＩ Ｍ片段为探针,通过Ｓｏｕｔｈｅｒｎ杂交将斜纹夜蛾核多角体病毒（Ｓｐｏｄｏｐｔｅｒａ ｌｉｔｕｒａ ｎｕｃｌｅａｒ ｐｏｌｙｈｅｄｒｏｓｉｓ ｖｉｒｕｓ,ＳｐｌｔＮＰＶ）的ｃｈｉ     

保幼激素类似物对斜纹夜蛾核多角体病毒增殖的影响

分别用5×10⁶,1×10⁷,5×10⁷,1×10⁸ PIBs/mL 4种浓度的斜纹夜蛾核多角体病毒(SpltNPV)感染斜纹夜蛾末龄幼虫（第6龄）,并于同龄期以10μg/头的保幼激素类似物(JHA) methoprene分别对各感染组进行点滴处理,以研究JHA对SpltNPV增殖的影响。研究表明,与对照组相比各不同浓度处理组病毒总产量分别提高227.06%、128.71%、52.62%、33.15%,平均单头病毒含量分别提高49.15%、48.40%、36.40%和31.11%,病毒感染死亡率分别提高119.21%、52.72%、12.64%和1.12%。其中以1×10.7 PIBs/mL感染再经JHA处理的病毒总产量和平均单头病毒含量最高,分别为1 701.8×10⁸PIBs和60.1×10⁸ PIBs。各处理组的病毒总产量和平均单头病毒含量均显著高于其对照组。在此基础上,进一步研究了JHA对染毒与未染毒宿主消化生理的影响。结果表明,JHA处理不仅延长了6龄幼虫的寿命,增加了其取食量,而且还显著提高了幼虫的食物转化率和病毒产量。     

斜纹夜蛾核多角体病毒抑制苜蓿丫纹夜蛾核多角体病毒诱导的斜纹夜蛾细胞凋亡

野生型苜蓿丫纹夜蛾核多角体病毒(Autographa californica multicapsid nucleopolyhedrovirus, AcMNPV)感染斜纹夜蛾(Spodoptera litura)细胞系Sl-zsu-1,可引起典型的细胞凋亡;但可以在草地夜蛾(Spodoptera frugiperda)细胞Sf-9中复制并形成多角体.比较了AcMNPV p35基因在病毒感染两种细胞的复制和转录情况,认为p35在非受纳细胞中及时有效的表达能阻止细胞发生凋亡;共感染实验结果表明,斜纹夜蛾核多角体病毒(Spodoptera litura multicapsid nucleopolyhedrovirus, SpltMNPV)可以抑制AcMNPV诱导的细胞凋亡并可帮助病毒进行复制,推测SpltMNPV基因组中与p35同源的p49基因挽救了细胞的自杀行为.     

斜纹夜蛾核多角体病毒几丁质酶基因上游4.0kb的序列分析

本文报道了斜 诳蛾核多角体病毒几丁质酶基因（chiA）上游约4.0kb范围内的序列,它包括了六个读码框（ORF1－6）,其长度分别为156bp、279bp、540bp、369bp、1281bp和228bp,可编码的氨基酸长度分别为51、98、179、122、426和75个,分子量分别为6.15kD、11.46kD、21.70kD、14.69kD 、47.59kD和9.09kD。在ORF1ORF2、ORF3起始密码前分别有一个、二个及一个杆状病毒早期启动子基序CAGT;在ORF4、ORF5起始密码前各有一个及二个杆状病毒晚期启动子基序TAAG。在ORF1、ORF4、ORF5终止密码下游有真核生物mRNA转录poly（A)加尾信号。ORF4为AcMNPV ORF53、BmNPV ORF42、OpMNPV ORF56、LdMNPV ORF54的同源基因。ORF1、ORF2、ORF6与已知的杆状病毒基因沿有同源性,可能为三个新的基因。     

斜纹夜蛾核型多角体病毒分子生物学研究进展

斜纹夜蛾核型多角体病毒(Spodoptera lituramulticapsid nucleopolyhedrovirus,SpltMNPV)属NPV科A亚群。近几年有关该病毒的序列测定、基因结构、功能和表达调控等系统的分子生物学研究工作进展迅速,特别是对一些重要基因的结构分析,有助于筛选毒力较强的杀虫毒株,并为这一病毒杀虫剂的改良和发展以及组建昆虫杆状病毒表达载体奠定基础。综述了与SpltMNPV相关的分子生物学领域的研究进展。     

“三明治”杂交法对斜纹夜蛾核型多角体病毒DNA克隆株的鉴定

用限制性内切酶HindⅢ将斜纹夜蛾核型多角体病毒DNA切割为A、B、C、D_1、D_2、E、F七个片段,与载体pUC18体外连接后转化大肠杆菌TG_1。通过“三明治“杂交法鉴定,分别获得七个片段的克隆株。但A片段克隆株中外源DNA片段发生了缺失。     

斜纹夜蛾核多角体病毒几丁质酶基因上游4.0kb的序列分析

本文报道了斜纹夜蛾核多角体病毒几丁质酶基因(chiA)上游约4.0 kb范围内的序列,它包括了六个读码框(ORF1～6),其长度分别为156 bp、297 bp、540 bp、369 bp、1281 bp和228 bp,可编码的氨基酸长度分别为51、98、179、122、426和75个,分子量分别为6.15?kD、11.46 kD、21.70 kD、14.69 kD、47.59 kD和9.09 kD。在ORF1、ORF2、ORF3起始密码前分别有一个、二个及一个杆状病毒早期启动子基序CAGT;在ORF4、ORF5起始密码前各有一个及二个杆状病毒晚期启动子基序TAAG。在ORF1、ORF4、ORF5终止密码下游有真核生物mRNA转录poly(A)加尾信号。ORF4为AcMNPVORF53、BmNPVORF42、OpMNPVORF56、LdMNPVORF54的同源基因。ORF1、ORF2、ORF6与已知的杆状病毒基因没有同源性,可能为三个新的基因。     

自然界斜纹夜蛾核型多角体病毒的基因型多态性

【目的】从基因组序列角度进一步揭示自然界斜纹夜蛾核型多角体病毒（Spodoptera litura nucleopolyhedrovirus, SpltNPV）的基因型多态性。【方法】病毒克隆A5, F1, X3 和 X15分别以活体克隆法分离自SpltNPV埃及株、 日本福冈株和日本小笠原株。根据SpltNPV基因组全序列（GenBank登录号: AF325155）和海灰翅夜蛾核型多角体病毒（S. littoralis NPV, SpliNPV）部分基因序列（GenBank登录号: X99377, X99376 和X98924）设计引物, PCR扩增获得A5, F1, X3 和 X15的多角体蛋白（polyhedrin, polh）基因和ORF18~ORF23序列。【结果】根据多角体蛋白基因序列, X3和X15属于SpltNPV型, 而A5和F1属于SpliNPV型。将A5, F1, X3 和 X15的ORF18~ORF23与SpltNPV和SpliNPV相应的基因序列进行同源性比较。结果发现, F1与SpliNPV以及X3与SpltNPV的核苷酸序列相似性高, 但X3的ORF20在172~558 nt处缺失387 bp。尽管依据多角体蛋白基因序列X15属于SpltNPV型, 但对于ORF18~ORF23序列, X15与SpliNPV的相似性高于与SpltNPV的相似性。同样, A5属于SpliNPV型, ORF18~ORF20与SpliNPV相应的核苷酸序列相似性高, 但ORF21与SpltNPV相应的核苷酸序列一致性为100%, 特别是ORF22, SpltNPV的特有序列出现在A5的基因组中, 而且与SpltNPV的ORF22一致性为100%; 反过来, ORF23又与SpliNPV相应的核苷酸序列相似性高。【结论】所有这些都表明, SpltNPV在自然界不仅存在基因型多态性, 而且即使属于同一基因型, 它们的基因组序列也有显著差异。可利用SpltNPV在自然界的这种异质性筛选适宜防治斜纹夜蛾幼虫的株系。     

Interaction of Xestia c-nigrum granulovirus with peritrophic matrix and Spodoptera litura nucleopolyhedrovirus in Spodoptera litura

Xestia c-nigrum granulovirus (XcGV) was tested for its ability to increase Spodoptera litura nucleopolyhedrovirus (SINPV) infection in larvae of S. litura (F.). The interaction of XcGV with peritrophic matrix and SINPV in S. litura also was studied to account for the synergism. In dose-response bioassays with a constant XcGV concentration of 5-mg/ ml capsules and SINPV concentration that varied from 10(3) to 10(7) polyhedral inclusion bodies (PIB) per larva, XcGV increased the virulence of SINPV infection in fifth instars of S. litura. The lethal concentration of 50% individuals (LC50) of SINPV combined with XcGV was 3.35 x 10(5)PIB/ml, which was significantly lower than that of SINPV alone (2.17 x 10(6)). Compared with 10(7) PIB/ml SINPV alone, the lethal time of 50% individuals (LT50) of 10(7) PIB/ml SINPV combined with XcGV was not significantly shortened. In addition, no significant improvement in the activity and killing speed of SINPV progeny was noted after propagation with XcGV, indicating that native characters of SINPV associated with viral potency were not altered by XcGV. Investigation via environmental scanning electronic microscopy showed that the peritrophic matrix (PM) of S. litura exposed to XcGV or XcGV enhancin, or the combination treatment, was markedly disrupted. The outer surface of the PM was loose, or ruptured, which potentially facilitated the passage of virions through the PM. Therefore, it is reasonable to conclude that the synergy between XcGV and SINPV was closely associated with the disruption of the PM in S. litura.     

Identification and expression of a conserved ubiquitin gene homologue of Spodoptera litura nucleopolyhedrovirus (SpltNPV-I)

An ORF having a potential to code for a polypeptide of 79 amino acids has been identified within 993 nt sequence of 2 kb EcoRI-W fragment of Spodoptera litura nucleopolyhedrovirus (SpltNPV-I). Nucleotide and deduced amino acid sequence analyses showed its identity with the ubiquitin homologue of eukaryotes (79–80%), Melanoplus sanguinipes entomopoxvirus (76%) and other baculoviruses (72–89%). The ORF is under baculovirus late promoter motif RTAAG but unlike other baculoviruses, three such motifs at –6, –10 and –27 position are present in SpltNPV. The ORF expresses as a 10 kDa protein in E. coli and the purified recombinant protein showed crossreactivity with the rabbit anti-ubiquitin antibodies.     

斜纹夜蛾核型多角体病毒ⅡORF146基因的克隆、表达与启动子活性分析

【目的】研究斜纹夜蛾核型多角体病毒II ORF146基因的结构与功能。【方法】根据SpltMNPV IIORF146基因序列设计引物,经PCR扩增克隆ORF146基因。在生物信息学分析基础上进行启动子活性分析和转录时相分析。构建ORF146片段的原核表达载体,表达并纯化融合蛋白后制备多克隆抗体。【结果】核苷酸序列分析表明,读码框含1383 bp,编码460个氨基酸的蛋白质,推定分子量为50.4 kDa。启动子活性分析和转录时相分析都表明该基因是个早、晚期都表达的基因,在病毒感染8 h和18 h有两个转录峰,24 h以后转录水平略有下降,但趋于稳定。pET-28a-ORF13原核表达的融合蛋白经纯化后制备的多克隆抗体特异性高,效价可达1∶3200以上。【结论】SpltMNPV II ORF146基因是一个早期和晚期都表达的病毒组成型结构蛋白基因。推测ORF146基因可能与SpltMNPV II病毒感染宿主细胞后病毒DNA复制有关。制备的多克隆抗体可用于深入研究该蛋白的生物学特性与功能。     

Insecticidal activity of the chitinase from the Spodoptera litura nucleopolyhedrovirus

Baculovirus chitinase gene (chiA) is a late gene essential for liquefying the host insect at a late stage of infection for its hydrolyzing chitin function. In a previous report, baculovirus ChiA has been shown to offer many interesting new opportunities for pest control. Recently, a putative chiA gene was identified in the Korean isolate of the Spodoptera litura nucleopolyhedorvirus (SpliMNPV‐K1) genome. The open reading frame (ORF) contains 1692 nucelotides and encodes a protein of 563 amino acids with a predicted molecular weight of about 62.6 kDa. To study the insecticidal activity of ChiA from SpliMNPV‐K1, we constructed a recombinant AcMNPV, Ap‐SlChiA, which is designed to express the ChiA under the control of a polyhedrin promoter. Western blot analysis indicated that ChiA was successfully expressed by this recombinant virus. Chitinase assay revealed that the chitobiosidase and endochitinase activity of the recombinant virus was 2.5‐ and 3.9‐flods higher than those of wild‐type AcMNPV, respectively. In addition, the recombinant virus showed higher evident insecticidal activity against 3rd instar larvae of Spodotera exigua than that of the AcMNPV. These results suggest that the chiA gene from SpliMNPV‐K1 could be successfully applied to improve pathogenicity of baculoviruses.     

Identification and expression of a conserved ubiquitin gene homologue of Spodoptera litura nucleopolyhedrovirus (spltNPV-I)

An ORF having a potential to code for a polypeptide of 79 amino acids has been identified within 993 nt sequence of 2 kb EcoRI-W fragment of Spodoptera litura nucleopolyhedrovirus (SpltNPV-I). Nucleotide and deduced amino acid sequence analyses showed its identity with the ubiquitin homologue of eukaryotes (79-80%), Melanoplus sanguinipes entomopoxvirus (76%) and other baculoviruses (72-89%). The ORF is under baculovirus late promoter motif RTAAG but unlike other baculoviruses, three such motifs at -6, -10 and -27 position are present in SpltNPV. The ORF expresses as a 10 kDa proteinin E. coli and the purified recombinant protein showed crossreactivity with the rabbit anti-ubiquitin antibodies.     

斜纹夜蛾核型多角体病毒不同分离株基因序列的同源性分析

研究SpltMNPV不同分离株及SpltMNPV分离株与SpliNPV间基因序列的同源性,为SpltMNPV分离株的利用提供理论基础。根据已发表的斜纹夜蛾核型多角体病毒（SpltMNPV）中国株（Zh）基因组全序列（AF527603）和海灰翅夜蛾核型多角体病毒（SpliNPV）Not I-D片段序列（AF527603）设计引物,PCR方法扩增得到SpltMNPV日本福冈株（Fu）、埃及株（Eg）和小笠原株（Og）的ORF39～ORF42和ORF119～ORF124编码区全序列。SpltMNPV不同分离株及SpltMNPV分离株与SpliNPV间基因序列的相似性比较, Zh株和Og株,Eg株、Fu株和SpliNPV的相似性高,而Zh株和Eg株、Fu株或SpliNPV,Og株和Eg株、Fu株或SpliNPV的相似性都比较低。亦即SpltMNPV 3种基因型,B型和C型的同源性高,A型与B型或C型的同源性比较低,但A型与SpliNPV的同源性高;同一基因型内不同分离株（Eg株和Fu株）的同源性高。ETG分子进化分析表明Eg株、Fu株和SpliNPV处于一个分支,而Eg株、Fu株和SpliNPV与Zh株和Og株则处于不同的分支。因此推断Eg株和Fu株为SpliNPV的分离株,而Og株为SpltMNPV的分离株。