R. F. Corrêa, R. S. Aguiar, R. Monnerat, B. Ribeiro
{"title":"苏云金芽孢杆菌亚种Cry4aa和cry4ba。重组杆状病毒在昆虫细胞中表达的以色列蚊对埃及伊蚊幼虫具有毒性","authors":"R. F. Corrêa, R. S. Aguiar, R. Monnerat, B. Ribeiro","doi":"10.17525/vrr.v18i1-2.70","DOIUrl":null,"url":null,"abstract":"Bacillus thuringiensis subsp. israelensis (Bti) is highly toxic to mosquito larvae. Most of its toxicity relies on δ-endotoxins (Cry and Cyt) crystalline inclusions produced at the sporulation phase of growth. Obtention of individual Bti mosquitocidal toxins is crucial for the understanding of Bti´s potential activity against dipteran larvae. A Cry toxin expression system based on baculovirus was developed to produce two of the Cry toxins comprised in the crystals of Bti. Th e cry4Aa and cry4Ba genes from two Brazilian strains of Bacillus thuringiensis were amplified by PCR, cloned into a plasmid cloning vector and sequenced. Sequence analysis of the cry4Aa and cry4Ba genes showed high identity to previous known cry genes. Both cry4Aa and cry4Ba genes were further cloned into transfer vectors for construction of recombinant baculoviruses. After isolation of the recombinant viruses, they were used to infect insect cells (BTITN5B1-4) that were analyzed by light microscopy at different times post infection. Putative crystals consisting of either Cry4Aa or Cry4Ba were observed in the cytoplasm of infected insect cells. RT-PCR was performed with mRNA from insect cell extracts (72 h.p.i.) in order to confirm the presence of the genes specific transcripts. Recombinant virus-infected insect extracts (120 h.p.i.) were analyzed by polyacrylamide gel electrophoresis (SDS-PAGE) showing the presence of polypeptide bands of around 128 and 130 kDa, corresponding, respectively to the sizes of the proteins Cry4Aa and Cry4Ba. Bioassays with virus-infected insect extracts were shown to be toxic to second instar Aedes aegypti larvae, confirming the usefulness of this expression system for the study of Cry proteins. DOI: http://dx.doi.org/10.17525/vrr.v18i1-2.70","PeriodicalId":30621,"journal":{"name":"Virus Reviews Research","volume":"31 1","pages":"5"},"PeriodicalIF":0.0000,"publicationDate":"2013-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CRY4AA AND CRY4BA FROM BACILLUS THURINGIENSIS SUBSP. ISRAELENSIS EXPRESSED IN INSECT CELLS BY RECOMBINANT BACULOVIRUSES ARE TOXIC TO AEDES AEGYPTI LARVAE\",\"authors\":\"R. F. Corrêa, R. S. Aguiar, R. Monnerat, B. Ribeiro\",\"doi\":\"10.17525/vrr.v18i1-2.70\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Bacillus thuringiensis subsp. israelensis (Bti) is highly toxic to mosquito larvae. Most of its toxicity relies on δ-endotoxins (Cry and Cyt) crystalline inclusions produced at the sporulation phase of growth. Obtention of individual Bti mosquitocidal toxins is crucial for the understanding of Bti´s potential activity against dipteran larvae. A Cry toxin expression system based on baculovirus was developed to produce two of the Cry toxins comprised in the crystals of Bti. Th e cry4Aa and cry4Ba genes from two Brazilian strains of Bacillus thuringiensis were amplified by PCR, cloned into a plasmid cloning vector and sequenced. Sequence analysis of the cry4Aa and cry4Ba genes showed high identity to previous known cry genes. Both cry4Aa and cry4Ba genes were further cloned into transfer vectors for construction of recombinant baculoviruses. After isolation of the recombinant viruses, they were used to infect insect cells (BTITN5B1-4) that were analyzed by light microscopy at different times post infection. Putative crystals consisting of either Cry4Aa or Cry4Ba were observed in the cytoplasm of infected insect cells. RT-PCR was performed with mRNA from insect cell extracts (72 h.p.i.) in order to confirm the presence of the genes specific transcripts. Recombinant virus-infected insect extracts (120 h.p.i.) were analyzed by polyacrylamide gel electrophoresis (SDS-PAGE) showing the presence of polypeptide bands of around 128 and 130 kDa, corresponding, respectively to the sizes of the proteins Cry4Aa and Cry4Ba. Bioassays with virus-infected insect extracts were shown to be toxic to second instar Aedes aegypti larvae, confirming the usefulness of this expression system for the study of Cry proteins. 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引用次数: 0
摘要
苏云金芽孢杆菌亚种以色列蚊(Bti)对蚊子幼虫有剧毒。其毒性主要依赖于产孢期产生的δ-内毒素(Cry和Cyt)晶体内含物。对蚊胺个体灭蚊毒素的研究是了解蚊胺对双翅目幼虫潜在活性的关键。建立了一种基于杆状病毒的Cry毒素表达系统,可产生两种含有Bti晶体的Cry毒素。采用PCR扩增苏云金芽孢杆菌巴西菌株cry4Aa和cry4Ba基因,并将其克隆到质粒克隆载体上进行测序。cry4Aa和cry4Ba基因序列分析表明,cry4Aa和cry4Ba基因与已知的cry4Ba基因具有较高的同源性。进一步将cry4Aa和cry4Ba基因克隆到重组杆状病毒的转移载体上。重组病毒分离后感染昆虫细胞(BTITN5B1-4),感染后不同时间光镜下进行分析。在被感染的昆虫细胞质中观察到由Cry4Aa或Cry4Ba组成的晶体。用昆虫细胞提取物(72 hp .i.)的mRNA进行RT-PCR,以确认基因特异性转录物的存在。通过聚丙烯酰胺凝胶电泳(SDS-PAGE)分析了重组病毒感染的昆虫提取物(120 hp .i.),发现存在约128和130 kDa的多肽带,分别与Cry4Aa和Cry4Ba蛋白的大小相对应。用病毒感染的昆虫提取物进行生物测定,结果显示对2龄埃及伊蚊幼虫具有毒性,证实了该表达系统在Cry蛋白研究中的有效性。DOI: http://dx.doi.org/10.17525/vrr.v18i1 - 2.70
CRY4AA AND CRY4BA FROM BACILLUS THURINGIENSIS SUBSP. ISRAELENSIS EXPRESSED IN INSECT CELLS BY RECOMBINANT BACULOVIRUSES ARE TOXIC TO AEDES AEGYPTI LARVAE
Bacillus thuringiensis subsp. israelensis (Bti) is highly toxic to mosquito larvae. Most of its toxicity relies on δ-endotoxins (Cry and Cyt) crystalline inclusions produced at the sporulation phase of growth. Obtention of individual Bti mosquitocidal toxins is crucial for the understanding of Bti´s potential activity against dipteran larvae. A Cry toxin expression system based on baculovirus was developed to produce two of the Cry toxins comprised in the crystals of Bti. Th e cry4Aa and cry4Ba genes from two Brazilian strains of Bacillus thuringiensis were amplified by PCR, cloned into a plasmid cloning vector and sequenced. Sequence analysis of the cry4Aa and cry4Ba genes showed high identity to previous known cry genes. Both cry4Aa and cry4Ba genes were further cloned into transfer vectors for construction of recombinant baculoviruses. After isolation of the recombinant viruses, they were used to infect insect cells (BTITN5B1-4) that were analyzed by light microscopy at different times post infection. Putative crystals consisting of either Cry4Aa or Cry4Ba were observed in the cytoplasm of infected insect cells. RT-PCR was performed with mRNA from insect cell extracts (72 h.p.i.) in order to confirm the presence of the genes specific transcripts. Recombinant virus-infected insect extracts (120 h.p.i.) were analyzed by polyacrylamide gel electrophoresis (SDS-PAGE) showing the presence of polypeptide bands of around 128 and 130 kDa, corresponding, respectively to the sizes of the proteins Cry4Aa and Cry4Ba. Bioassays with virus-infected insect extracts were shown to be toxic to second instar Aedes aegypti larvae, confirming the usefulness of this expression system for the study of Cry proteins. DOI: http://dx.doi.org/10.17525/vrr.v18i1-2.70