Co-operational PCR coupled with dot blot hybridization for detection and 16SrX grouping of phytoplasmas

被引：10

作者：

Bertolini, E.

Torres, E.

Olmos, A.

Martin, M. P.

Bertaccini, A.

Cambra, M.

机构：

[1] IVIA, Dept Protecc Vegetal & Biotechnol, Valencia 46113, Spain

[2] Dept Agr Alimentac & Accio Rural, Barcelona 08004, Spain

[3] CSIC, Dept Micol, Madrid 28014, Spain

[4] Univ Bologna, DISTA, Bologna, Italy

来源：

PLANT PATHOLOGY | 2007年 / 56卷 / 04期

关键词：

'Ca. Phytoplasma mali'; 'Ca. Phytoplasma prunorum'; 'Ca. Phytoplasma pyri'; DNA targets; molecular detection and diagnostics; nested PCR;

D O I：

10.1111/j.1365-3059.2007.01601.x

中图分类号：

S3 [农学（农艺学）];

学科分类号：

0901 ;

摘要：

A protocol based on Co-operational PCR has been successfully applied to the detection of phytoplasmas. A triprimer reaction coupled with hybridization using general and specific probes permitted detection of 'Candidatus Phytoplasma mali', 'Ca. Phytoplasma prunorum' and 'Ca. Phytoplasma pyri', and their identification as members of 16S ribosomal quarantine group X. The sensitivity of this method was at least one hundred times greater than conventional PCR and similar to that achieved by nested PCR and real-time PCR. The method was validated by testing field samples collected from Malus, Prunus and Pyrus spp. and Olea europaea and compared with seven phytoplasmas maintained in Catbaranthus roseus.

引用

页码：677 / 682

页数：6

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