Dai Y C, Korhonen K
Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang 110016, China.
Finnish Forest Research Institute, P.O. Box 18, FIN-01301 Vantaa, Finland.
Plant Dis. 2003 Aug;87(8):1007. doi: 10.1094/PDIS.2003.87.8.1007B.
Members of the Heterobasidion annosum (Fr.) Bref. complex are among the most important pathogens in coniferous forests of Europe and North America. Three intersterile groups (P, S, and F) have been found in this complex from Europe (1) and were recently segregated into three species based on intersterility, host preferences, and morphology (4). In a survey of wood-rotting fungi in China in 2002, Heterobasidion spp. were found on Tsuga chinensis (Franch.) Pritz and T. dumosa (D. Don) Eichl. in natural forests from the northern Sichuan Province of southwestern China (32°43' to 33°11' N, 103°50' to 103°53' E.). Basidiocarps of the fungus were relatively common on decayed wood in roots of dead trees, stumps, and fallen trunks. We collected four basidiocarps (Dai 4045, 4051, 4214, and 4224 in the Institute of Applied Ecology, Chinese Academy of Sciences, IFP) from three stands of mixed coniferous forests and made 40 homokaryotic, single-basidiospore cultures (02046, 02047, 02050, and 02051 in the Finnish Forest Research Institute). Two homokaryons from each basidiocarp were paired with homokaryotic tester strains of European H. annosum (P group), H. parviporum Niemelä & Korhonen (S group), and H. abietinum Niemelä & Korhonen (F group). The pairings showed that the progeny from the four basidiocarps are H. parviporum. The Chinese isolates did not form clamp connections with H. annosum sensu stricto, and a strong demarcation line developed in all these pairings. In contrast, the Chinese isolates formed clamp connections in almost every pairing with European H. parviporum, the clamp connections developed in both sides of the pairings, and no distinct demarcation line was present in most of these pairings. The Chinese homokaryons were also compatible with European H. abietinum, but in most of these pairings, clamp connections were found in the isolate from China but not in the European tester, and a demarcation line was present in most of the pairings. In contrast to H. annosum sensu stricto, the Chinese basidiocarps had smaller pores (4.5 to 6 per mm versus 3 to 4.5 per mm), and a thin tomentum on the pileal surface in contrast to the basidiocarps of H. abietinum. Previously, H. parviporum was found in Asia on coniferous hosts such as Abies, Larix, Picea and Pinus spp. (2). The North American S group of H. annosum sensu lato attacks species of Tsuga spp. in western North America (3), but to our knowledge, this is the first report of H. parviporum on native species of Tsuga spp. outside North America. References: (1) P. Capretti et al. Eur. J. For. Pathol. 20:231, 1990. (2) Y. C. Dai and K. Korhonen. Eur. J. For. Pathol. 29:273, 1999. (3) G. M. Filip and D. J. Morrison. North America. Pages 405-427 in: Heterobasidion annosum. Biology, Ecology, Impact and Control. CAB International, Wallingford, UK, 1998. (4) T. Niemelä and K. Korhonen. Taxonomy of the genus Heterobasidion. Pages 27-33 in: Heterobasidion annosum. Biology, Ecology, Impact and Control. CAB International, Wallingford, UK, 1998.
异担子菌(Heterobasidion annosum (Fr.) Bref.)复合种的成员是欧洲和北美针叶林中最重要的病原菌之一。在欧洲的该复合种中已发现三个不育组(P、S和F)(1),并且最近根据不育性、寄主偏好和形态学将其划分为三个物种(4)。在2002年对中国木腐菌的一项调查中,在位于中国西南部四川省北部(北纬32°43′至33°11′,东经103°50′至103°53′)的天然林中的铁杉(Tsuga chinensis (Franch.) Pritz)和高山铁杉(T. dumosa (D. Don) Eichl.)上发现了异担子菌属(Heterobasidion spp.)。该真菌的担子果在死树根、树桩和倒下树干的腐朽木上相对常见。我们从三个针叶混交林分中采集了四个担子果(中国科学院应用生态研究所的戴4045、4051、4214和4224),并制备了40个同核体、单担孢子培养物(芬兰森林研究所的02046、02047、02050和02051)。将每个担子果的两个同核体与欧洲异担子菌(P组)、小孢异担子菌(H. parviporum Niemelä & Korhonen,S组)和冷杉异担子菌(H. abietinum Niemelä & Korhonen,F组)的同核测试菌株配对。配对结果表明,这四个担子果的后代是小孢异担子菌。中国分离株与狭义异担子菌不形成锁状联合,并且在所有这些配对中都形成了明显的分界线。相比之下,中国分离株与欧洲小孢异担子菌的几乎每一次配对中都形成了锁状联合,锁状联合在配对双方都有形成,并且在大多数这些配对中没有明显的分界线。中国同核体也与欧洲冷杉异担子菌相容,但在大多数这些配对中,在中国分离株中发现了锁状联合,而在欧洲测试菌株中未发现,并且在大多数配对中存在分界线。与狭义异担子菌相比,中国的担子果有较小的菌孔(每毫米4.5至6个,而狭义异担子菌为每毫米3至4.5个),并且菌盖表面有一层薄绒毛,这与冷杉异担子菌的担子果不同。此前,小孢异担子菌在亚洲的针叶寄主如冷杉属(Abies)、落叶松属(Larix)、云杉属(Picea)和松属(Pinus)物种上被发现(2)。北美广义异担子菌的S组在北美西部侵袭铁杉属物种(3),但据我们所知,这是小孢异担子菌在北美以外地区的铁杉属本地物种上的首次报道。参考文献:(1)P. Capretti等人,《欧洲森林病理学杂志》20:231,1990年。(2)戴玉成和K. Korhonen,《欧洲森林病理学杂志》29:273,1999年。(3)G. M. Filip和D. J. Morrison,《北美》。载于:《异担子菌》。生物学、生态学、影响与控制。CAB国际出版社,英国沃灵福德,1998年,第405 - 至427页。(4)T. Niemelä和K. Korhonen,《异担子菌属的分类学》。载于:《异担子菌》。生物学、生态学、影响与控制。CAB国际出版社,英国沃灵福德,1998年,第27 - 33页。