First report of Neocosmospora vasinfecta associated with the root rot complex of peanuts in Vietnam V. T. Dau A , L. T. Pham A , T. M. Luong B , L. M. T. Huynh B , NT Tran C , T. D. Ho D , H. M. T. Hoang D , H. T. Phan E and L. W. Burgess F,G A Nghe An Plant Protection Sub-Department, Vinh, Nghe An, Vietnam. B Quang Nam Plant Protection Sub-Department, Tam Ky, Quang Nam, Vietnam. C College of Agriculture and Forestry, Hue University, Hue, TT Hue, Vietnam. D TTHue Plant Protection Sub-Department, Hue, Vietnam. E National Institute of Medicinal Materials, Hanoi, Vietnam. F Faculty of Agriculture, Food and Natural Resources, The University of Sydney, NSW 2006, Australia. G Corresponding author. Email: burgess.international@gmail.com Abstract. The occurrence of Neocosmospora vasinfecta is reported for the rst time from Vietnam where it was found in association with peanut roots affected by root rot. It was isolated from diseased roots from peanut crops in Nghe An Province in March 2007 but perithecia were not observed on the diseased roots. However, characteristic perithecia were produced abundantly in pure cultures on potato dextrose agar and carnation leaf-piece agar. Subsequently, perithecia were observed on diseased peanut roots in Thua Thien Hue Province. Representative cultures from Nghe An were conrmed as Neocosmospora vasinfecta by the Centraalbureau voor Schimmelcultures (CBS). Diagnostic studies were undertaken on the fungal pathogens associated with the root, crown and stem rot complex of peanuts in Nghe An, Quang Nam and Thua Thien Hue Provinces, Vietnam, in the growing seasons of 2006 and 2007. These involved ad hoc surveys to document symptoms and collect samples of root, crown and stem rots for isolation and identication of putative fungal pathogens, using procedures described in Burgess et al.(2008). Root rot samples were washed in tap water, surface sterilised in 70% ethyl alcohol for 5 s, immediately rinsed in sterile water and damp-dried on sterile paper tissues. Sections of root (23 mm) were removed from the margin of diseased and symptomless tissue and plated on water agar containing streptomycin sulfate (1.0 g/L) and neomycin sulfate (0.12 g/L). Colonies that developed from the sections were transferred to carnation leaf- piece agar (CLA), and then puried by hyphal tipping (Burgess et al. 2008) to CLA and potato dextrose agar (PDA). Some cultures, putatively identied as Neocosmospora vasinfecta, produced abundant orange-red perithecia in the mycelium in colonies on PDA (Fig. 1) and on leaf pieces in CLA (Fig. 2). The perithecia contained thin-walled cylindrical asci. The eight globose to ellipsoidal ascospores were uniseriately arranged in the ascus (Fig. 3). The anamorph stage, small cylindrical to oblong-ellipsoidal, hyaline, one-celled conidia were formed in false-heads on long, thin, sometimes branched, conidiophores (Fig. 4) arising from vegetative mycelium, on both media. These morphological features corresponded to the description of N. vasinfecta in Cannon and Hawksworth (1984). Nine putative cultures of N. vasinfecta from Nghe An Province were forwarded to the Centraalbureau voor Schimmelcultures (CBS) where the identication of eight cultures was conrmed by sequencing. They were identical to each other and related to AY381142. The Nghe An Plant Protection Sub-Department accession numbers (NA prex), and the corresponding CBS Fig. 1. Abundant orange-red perithecia of Neocosmospora vasinfecta forming in a colony on potato dextrose agar. CSIRO PUBLISHING www.publish.csiro.au/journals/apdn Australasian Plant Disease Notes, 2010, 5, 7981 Ó Australasian Plant Pathology Society 2010 10.1071/DN10028 1833-928X/10/010079