首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Use of Quantitative PCR Detection Methods to Study Biocontrol Agents and Phytopathogenic Fungi and Oomycetes in Environmental Samples
Authors:Simona M Sanzani  Maria G Li Destri Nicosia  Roberto Faedda  Santa O Cacciola  Leonardo Schena
Institution:1. Dipartimento di Scienze del Suolo, della Pianta e degli Alimenti, Università degli Studi Aldo Moro, , 70126 Bari, Italy;2. Dipartimento di Agraria, Università Mediterranea di Reggio Calabria, , 89124 Reggio Calabria, Italy;3. Dipartimento di Gestione dei Sistemi Agroalimentari e Ambientali, Università degli Studi, , 95123 Catania, Italy
Abstract:Quantitative polymerase chain reaction (qPCR) is a versatile technique for the accurate, sensitive, reliable and high‐throughput detection and quantification of target DNA in various environmental samples, and in recent years, it has greatly contributed to the advancement of knowledge in the plant pathology field. Indeed, this technique is ideal to evaluate inoculum threshold levels and to study the epidemiology, biology and ecology of phytopathogenic fungi and oomycetes, thus opening up new research opportunities to investigate host–pathogen interactions and to address tasks related to quarantine, eradication and biosecurity. Moreover, it can be a useful tool in breeding programs. The present review analyses the most relevant applications of qPCR for the detection and quantification of filamentous fungi and oomycetes within host tissues and in soil, air and water, along with brief paragraphs focusing on new application fields such as the detection and quantification of mycotoxigenic fungi and biocontrol agents. The high potentiality of qPCR for present and future applications is highlighted together with a critical analysis of major drawbacks that need to be corrected to definitively confirm it as a preferential routine quantitative detection method.
Keywords:biocontrol agents  detection  mycotoxigenic fungi  phytopathogenic fungi  phytopathogenic oomycetes  qPCR  quantitative analyses
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号