Alkan Mehtap, Özer Göksel, Mustafa İmren, Ozdemir Fatih, Morgounov Alexei, Dababat Abdelfattah A
Bolu Abant Izzet Baysal University, Department of Plant Protection, Bolu Abant Izzet Baysal Universitesi Golkoy Yerleskesi, Bolu, Turkey, 14280.
Turkey;
Plant Dis. 2021 Mar 3. doi: 10.1094/PDIS-12-20-2659-PDN.
Triticale (×Triticosecale Wittmack) is obtained from wheat × rye crossing. It is positioned between wheat and rye in terms of resistance to soilborne pathogens including Gaeumannomyces graminis var. tritici, Fusarium culmorum, F. avenaceum, and Bipolaris sorokiniana (Arseniuk and Góral 2015). In 2019, seven triticale fields were surveyed in Almaty Province, Kazakhstan to examine soil-borne fungal pathogens. A total of 28 symptomatic plants with stunting, rot or discolored root were collected to identify causal agents. The overall disease incidence was approximately 8 to 10% in the fields. Fungi were isolated from 3-5 mm pieces excised from symptomatic tissues. The pieces were exposed to surface disinfection in 1% sodium hypochlorite solution for 2 min, rinsed three times with sterile distilled water, blotted dry, and plated on 1/5 strength potato dextrose agar (PDA) amended with 0.01% streptomycin. Plates were left in the dark at 23°C for 7 days. A total of 34 fungal colonies were isolated of which nineteen isolates, originally from six fields showed the cultural characteristics of B. sorokiniana. This species was previously reported to cause common root rot on triticale in Kazakhstan (Özer et al. 2020). Ten isolates from four fields produced pale orange and cottony mycelium with red pigmentation on the agar, which is typical of Fusarium-like growth. The remaining isolates (n=5) from two fields produced salmon-colored and scarce aerial mycelium with no soluble pigmentation, similar to Microdochium spp. Fusarium isolates produced thick-walled and curved macroconidia with 3-4 septa (n=50, 25.7 to 37.6 × 4.1 to 7.3 μm in size) and notched basal cell on PDA, but microconidia were absent, which matches the description of F. culmorum (Wm.G. Sm.) Sacc. (Leslie and Summerell 2006). Microdochium isolates produced swollen, brown, and thick-walled chlamydospores and hyaline, one-celled, and thin-walled conidia (n=50, 5.4 to 9.3 × 1.5 to 3.0 μm in size) formed on ampullate and cylindrical conidiogenous cells on oatmeal agar (OA). These morphological features are consistent with previous observations for Microdochium bolleyi (R. Sprague) de Hoog & Herm.-Nijh. (Hong et al. 2008). To confirm morphological preliminary identifications, the portion of the translation elongation factor 1-alpha (EF1-α) gene was amplified with EF1/EF2 primers (O'Donnell et al. 1998) for representative Fusarium isolates (n=4) for each field. Additionally, the internal transcribed spacer (ITS) of ribosomal DNA was amplified with ITS1/ITS4 primers (White et al. 1990) for representative Microdochium isolates (n=2) for each field. BLASTn queries against NCBI GenBank revealed that the EF1-α sequences of Fusarium isolates (MW311081-MW311084) shared 100% identity with F. culmorum strain CBS 110262 (KT008433). The ITS sequences of M. bolleyi isolates (MW301448-MW301449) matched that of M. bolleyi strain CBS 137.64 (AM502264) with 100% sequence similarity. Pathogenicity test was conducted on pregerminated seeds of triticale cv. Balausa. A plastic pot (17 cm height, 9 cm in diam) was filled with a sterile mixture of vermiculite, peat, and soil (1:1:1, v/v/v). Mycelial plugs (1 cm in diam) were cut from the margin of a growing culture of representative isolates (Kaz_Fus123 and Kaz_Mb01) and placed onto the mixture in the pot. A sterile agar plug was employed as a control treatment. One pregerminated seed was put on the plug and covered with the mixture. The pots were transferred to a growth chamber set at 23 ± 2°C and a photoperiod of 14 hours. The experiment was performed twice using 5 replication pots per isolate. Four weeks after inoculation, discoloration of the crown was observed on all the inoculated roots, whereas no symptoms were observed on the control plants. Koch's postulates were fulfilled by reisolating and identifying the pathogen based on the morphology described above. This is the first report of M. bolleyi and F. culmorum causing root rot on triticale in Kazakhstan. Although B. sorokiniana is the most primary pathogen that may limit yield in the production of triticale in Kazakhstan, F. culmorum and M. bolleyi have been found to be less frequent and less aggressive pathogens, respectively. Further studies are needed to better understand the potential distribution and impact of these pathogens on triticale.
小黑麦(×Triticosecale Wittmack)是由小麦与黑麦杂交获得的。在对包括禾顶囊壳小麦变种(Gaeumannomyces graminis var. tritici)、禾谷镰刀菌(Fusarium culmorum)、燕麦镰刀菌(F. avenaceum)和小麦根腐离蠕孢(Bipolaris sorokiniana)在内的土传病原菌的抗性方面,小黑麦介于小麦和黑麦之间(Arseniuk和Góral,2015年)。2019年,在哈萨克斯坦阿拉木图省对7个小黑麦田进行了调查,以检测土传真菌病原菌。总共采集了28株表现出矮化、腐烂或根部变色症状的植株,以鉴定致病因子。田间总体发病率约为8%至10%。从有症状组织上切取3 - 5毫米的片段分离真菌。将片段在1%次氯酸钠溶液中进行表面消毒2分钟,用无菌蒸馏水冲洗3次,吸干水分,接种到添加了0.01%链霉素的1/5强度马铃薯葡萄糖琼脂(PDA)平板上。平板在23°C黑暗条件下放置7天。共分离出34个真菌菌落,其中最初来自6个田块的19个分离株表现出小麦根腐离蠕孢的培养特征。该物种此前曾被报道在哈萨克斯坦导致小黑麦发生普通根腐病(Özer等人,2020年)。来自4个田块的10个分离株在琼脂上产生浅橙色和棉絮状菌丝体,并带有红色色素沉着,这是镰刀菌属样生长的典型特征。来自2个田块的其余分离株(n = 5)产生鲑鱼色且稀少的气生菌丝体,无可溶性色素沉着,类似于微dochium spp.。镰刀菌分离株在PDA上产生厚壁且弯曲的大型分生孢子,有3 - 4个隔膜(n = 50,大小为25.7至37.6×4.1至7.3微米),基部细胞有缺刻,但无小型分生孢子,这与禾谷镰刀菌(Wm.G. Sm.)Sacc.的描述相符(Leslie和Summerell,2006年)。微dochium分离株在燕麦粉琼脂(OA)上的瓶梗状和圆柱形分生孢子梗细胞上产生肿胀、褐色且厚壁的厚垣孢子以及透明、单细胞且薄壁的分生孢子(n = 50,大小为5.4至9.3×1.5至3.0微米)。这些形态特征与之前对博勒微dochium(R. Sprague)de Hoog & Herm.-Nijh.的观察结果一致(Hong等人,2008年)。为了确认形态学初步鉴定结果,使用EF1/EF2引物(O'Donnell等人,1998年)对每个田块的代表性镰刀菌分离株(n = 4)扩增翻译延伸因子1 - α(EF1 - α)基因的部分片段。此外,使用ITS1/ITS4引物(White等人,1990年)对每个田块的代表性微dochium分离株(n = 2)扩增核糖体DNA的内部转录间隔区(ITS)。对NCBI GenBank进行BLASTn查询显示,镰刀菌分离株的EF1 - α序列(MW311081 - MW311084)与禾谷镰刀菌菌株CBS 110262(KT008433)的序列一致性为100%。博勒微dochium分离株的ITS序列(MW301448 - MW301449)与博勒微dochium菌株CBS 137.64(AM502264)的序列相似性为100%。对小黑麦品种Balausa的预发芽种子进行了致病性测试。一个塑料盆(高17厘米,直径9厘米)装满了蛭石、泥炭和土壤的无菌混合物(1:1:1,v/v/v)。从代表性分离株(Kaz_Fus123和Kaz_Mb01)生长培养物的边缘切取直径1厘米的菌丝块,放置在盆中的混合物上。使用无菌琼脂块作为对照处理。将一粒预发芽的种子放在菌丝块上,并用混合物覆盖。将盆转移到设定温度为23±2°C、光周期为14小时的生长室中。每个分离株使用5个重复盆进行了两次实验。接种四周后,在所有接种的根上观察到冠部变色,而对照植株未观察到症状。通过基于上述形态学特征重新分离和鉴定病原菌,科赫法则得到了满足。这是博勒微dochium和禾谷镰刀菌在哈萨克斯坦导致小黑麦根腐病的首次报道。尽管小麦根腐离蠕孢是哈萨克斯坦小黑麦生产中可能限制产量的最主要病原菌,但已发现禾谷镰刀菌和博勒微dochium分别是较不常见且致病性较弱的病原菌。需要进一步研究以更好地了解这些病原菌在小黑麦上的潜在分布和影响。