Touchdown nested multiplex PCR detection of Phytophthora cinnamomi and P. cambivora from French and English chestnut grove soils

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• 作者：Stephen R.H. Langrell¹ ; ^{stephen.langrell@ec.europa.eu} ; Olivier Morel ; Cé ; cile Robin
• 关键词：Chestnut ; Detection ; Disease management ; Ink disease ; Nested-Polymerase Chain Reaction (PCR) ; Multiplex ; Touchdown ; Phythophthora cinnamomi ; Phythophthora cambivora ; Soil
• 刊名：Fungal Biology
• 出版年：2011
• 出版时间：July 2011
• 年：2011
• 卷：115
• 期：7
• 页码：672-682
• 全文大小：299 K

文摘

Soil borne Phytophthora cinnamomi and Phytophthora cambivora are considered the most pathogenic species associated with chestnut (Castanea sativa) decline in Europe. Mapping their incidence and distribution from nursery and plantation soils may offer valuable information for limiting spread. As conventional biological baiting and taxonomic confirmation is generally time consuming, labour, logistically and space intensive, we have focused on the development of a specific touchdown nested multiplex Polymerase Chain Reaction (PCR) approach for the simultaneous detection of both species direct from soil. Pre-existing and novel primers, based on Internal Transcribed Spacer (ITS) sequences, have been evaluated for their specificity and use in a multiplex capacity in various combinations. Coupled to this we have modified a mechanical lysis procedure for DNA extraction from up to 10 g of chestnut under storey soils (ranging from 0.5 to 25 ¦Ìg DNA g^? fresh soil). Using serial dilutions and/or polyvinylpolypyrrolidone chromatography purification, both species have been successfully detected, in artificially and naturally infected soils. Levels of assay detection are comparable to other Phytophthora species where PCR based diagnostic systems have been reported. A qualitative evaluation of this approach against conventional baiting is presented.