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一种属于16SrIII-A亚组的植原体和与巴西木薯蛙皮病相关的双链RNA病毒。

A Phytoplasma Belonging to a 16SrIII-A Subgroup and dsRNA Virus Associated with Cassava Frogskin Disease in Brazil.

作者信息

de Souza Adriana N, da Silva Fábio N, Bedendo Ivan P, Carvalho Claudine M

机构信息

Department of Plant Pathology, UFV, Viçosa, Brazil.

Department of Plant Pathology and Nematology, ESALQ/USP, Piracicaba, Brazil.

出版信息

Plant Dis. 2014 Jun;98(6):771-779. doi: 10.1094/PDIS-04-13-0440-RE.

Abstract

Cassava frogskin disease (CFSD) is a particular threat in cassava because symptoms remain hidden until harvest and losses can be total. The information related to the etiological agent of this disease is contradictory, because some authors believe it is caused by phytoplasmas while others believe that it is caused by a virus. In order to refine detection protocols and to characterize organisms associated with CFSD in Brazil, 32 symptomatic and 20 asymptomatic cassava plants were collected in Minas Gerais state. Total DNA was extracted and used for nested polymerase chain reaction (PCR) to detect phytoplasmas. Because endophytic Bacillus spp. led to false positives, primers were designed to facilitate the detection of phytoplasma in the presence of bacteria. In addition, double-stranded (ds)RNA was extracted from tubers and used in reverse-transcription PCR for the detection of the RNA-dependent RNA polymerase gene from Cassava frogskin virus segment 4. The detected phytoplasma was identified as belonging to the group 16SrIII-A by restriction fragment length polymorphism (RFLP), sequencing, and RFLP in silico. This is the first report of a phytoplasma belonging to the 16SrIII-A group associated with cassava plants, the first molecular characterization of a phytoplasma associated with CFSD in Brazil, and a first report of phytoplasma and a dsRNA virus (possible reovirus) co-infecting cassava plants with CFSD symptoms.

摘要

木薯蛙皮病(CFSD)对木薯构成了特殊威胁,因为其症状在收获前一直隐匿,可能导致全部损失。关于这种疾病病原体的信息相互矛盾,一些作者认为它是由植原体引起的,而另一些人则认为是由病毒引起的。为了完善检测方案并鉴定巴西与CFSD相关的生物体,在米纳斯吉拉斯州采集了32株有症状和20株无症状的木薯植株。提取总DNA并用于巢式聚合酶链反应(PCR)以检测植原体。由于内生芽孢杆菌属会导致假阳性,因此设计了引物以利于在存在细菌的情况下检测植原体。此外,从块根中提取双链(ds)RNA,并用于逆转录PCR,以检测木薯蛙皮病毒片段4的RNA依赖性RNA聚合酶基因。通过限制性片段长度多态性(RFLP)、测序和电子RFLP将检测到的植原体鉴定为属于16SrIII-A组。这是关于与木薯植株相关的16SrIII-A组植原体的首次报道,是巴西与CFSD相关植原体的首次分子特征描述,也是植原体和dsRNA病毒(可能是呼肠孤病毒)共同感染出现CFSD症状木薯植株的首次报道。

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