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A multi-locus backbone tree for Pestalotiopsis, with a polyphasic characterization of 14 new species

Sajeewa S. N. MaharachchikumburaInstitute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, ThailandLiang‐Dong GuoState Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, People’s Republic of ChinaLei CaiState Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, People’s Republic of ChinaEkachai ChukeatiroteInstitute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, ThailandWen WuXiang SunState Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, People’s Republic of ChinaP.W. CrousCBS-KNAW Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD, Utrecht, The NetherlandsD. Jayarama BhatDepartment of Botany, Goa University, Panaji, Goa, 403 206, IndiaEric H. C. McKenzieLandcare Research, Private Bag, 92170, Auckland, New ZealandAli H. BahkaliCollege of Science, Botany and Microbiology Department, King Saud University, P.O. Box: 2455, Riyadh, 1145, Saudi ArabiaKevin D. HydeInstitute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand
2012en
ABI

Аннотация

Pestalotiopsis is a taxonomically confused, pathogenic and chemically creative genus requiring a critical re-examination using a multi-gene phylogeny based on ex-type and ex-epitype cultures. In this study 40 isolates of Pestalotiopsis, comprised of 28 strains collected from living and dead plant material of various host plants from China were studied by means of morphology and analysis of ITS, β–tubulin and tef1 gene sequence data. Based on molecular and morphological data we describe 14 new species (Pestalotiopsis asiatica, P. chinensis, P. chrysea, P. clavata, P. diversiseta, P. ellipsospora, P. inflexa, P. intermedia, P. linearis, P. rosea, P. saprophyta, P. umberspora, P. unicolor and P. verruculosa) and three species are epitypified (P. adusta, P. clavispora and P. foedans). Of the 10 gene regions (ACT, β-tubulin, CAL, GPDH, GS, ITS, LSU, RPB 1, SSU and tef1) utilized to resolve cryptic Pestalotiopsis species, ITS, β–tubulin and tef1 proved to be the better markers. The other gene regions were less useful due to poor success in PCR amplification and/or in their ability to resolve species boundaries. As a single gene tef1 met the requirements for an ideal candidate and functions well for species delimitation due to its better species resolution and PCR success. Although β-tubulin showed fairly good differences among species, a combination of ITS, β-tubulin and tef1 gene data gave the best resolution as compared to single gene analysis. This work provides a backbone tree for 22 ex-type/epitypified species of Pestalotiopsis and can be used in future studies of the genus.

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