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First published on December 23, 2009
Mycologia 2009
DOI: 10.3852/09-243
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© 2009 by The Mycological Society of America

Trichoderma asperellum sensu lato consists of two cryptic species


Gary J. Samuels 1,*
Adnan Ismaiel 2
Marie-Claude Bon 3
Sophie De Respinis 4
Orlando Petrini 4

     1 Systematic Mycology & Microbiology lab, United States Department of Agriculture, Agricultural Research Service, Beltsville, Maryland, 20705, United States of America
2 USDA-ARS-SMML, Beltsville, MD
3 ARS-EBCL, Montferrier sur Lez, France
4 Cantonal Institute of Microbiology, 6500 Bellinzona,, TIcino, Switzerland

Analysis of a world-wide collection of strains of Trichoderma asperellum sensu lato using multilocus genealogies of four genomic regions (tef1, rpb2, act, ITS1, 2 and 5.8s rRNA), sequence polymorphism-derived (SPD) markers, matrix-assisted laser desorption/ionisation-time of flight mass spectrometry (MALDI-TOF MS) of the proteome, and classical mycological techniques revealed two morphologically cryptic sister species within T. asperellum, T. asperellum, T. asperelloides sp. nov., and a third closely related but morphologically distinct species. T. yunnanense. Trichoderma asperellum and T. asperelloides have wide sympatric distribution on multiple continents; T. yunnanense is represented by a single strain from China. Several strains reported in the literature or represented in GenBank as T. asperellum are reidentified as T. asperelloides. Four molecular SPD typing patterns (I-IV) were found over a large geographic range. Patterns I-III were only produced by T. asperellum and Pattern IV by T. asperelloides and T. yunnanense. Pattern I was found in North America, South America, Africa and Europe and Asia (Saudi Arabia). Pattern III was found in Africa, North America, South America and Asia, not in Europe. Pattern II was found only in Cameroon (Central Africa) and Peru. Pattern IV was found in all continents. All SPD II pattern strains formed a strongly supported subclade within the T. asperellum clade in the phylogenetic tree based on rpb2 and MLS (combined multilocus sequence). The diversity of DNA sequences, SPD markers and polypeptides in T. asperellum suggests that further speciation is underway within T. asperellum. MALDI-TOF MS distinguished T. yunnanense from related taxa by UPGMA clustering, but separation between T. asperellum and T. asperelloides was less clear.

Key words: MALDI-TOF MS, biological control, systematics, Hypocreales, biogeography


* Systematic Mycology & Microbiology lab, United States Department of Agriculture, Agricultural Research Service, Beltsville, Maryland, 20705, United States of America Gary.Samuels{at}ARS.USDA.GOV







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Copyright © 2009 by The Mycological Society of America.