Hua Yue, Zheng Zhijie, Wang Jianfei, Zhu Lin, Zhou Cheng
Anhui Science and Technology University, 177515, Chuzhou, Anhui, China;
Anhui Science and Technology University, 177515, Chuzhou, Anhui, China.
Plant Dis. 2023 Dec 15. doi: 10.1094/PDIS-05-23-0891-PDN.
Ginger (Zingiber officinale) is an important commercial crop that has been widely cultivated in China for more than 2500 years. One variety, Tongling white ginger, has been grown in the Yi'an District of Tongling city, Anhui province (30°45 N, 117°43 E), China. In August 2022, symptoms of yellowing and wilting were observed on ginger plants, with a disease incidence rate exceeding 20% in the field. The stem base of the diseased plants became soft, brown and water-soaked. Additionally, the rhizomes displayed symptoms of browning and water-soaked rot, resembling those caused by Ralstonia solanacearum and Enterobacter cloacae (Yu et al. 2003; Nishijima et al. 2004; Liu et al. 2021). Consequently, ginger bacterial wilt disease may potentially emerge from a combination of infections by diverse pathogenic bacteria. To identify novel pathogens causing the wilt disease, stem tissues of the diseased plants from different locations were sterilized with 1% sodium hypochlorite (NaOCl) for 10 min, followed by at least three time rinses with sterile water. The sterilized samples were then ground with 0.9% saline solution and left at room temperature for 30 min. A 20 μL aliquot of the suspension was serially diluted and cultured on Luria-Bertani (LB) medium at 28°C. A total of 217 isolates was picked and purified for taxonomic identification by 16S rRNA gene analyses with the primer 27F/1492R (Weisburg et al. 1991). Among these isolates, 23 single colony isolates were identified as A. xylosoxidans through NCBI BLASTn analyses. Furthermore, three single isolates from different locations were randomly selected for further experiments. The growing colonies appeared opaque white and round. Microscopic evaluation revealed that cells were rod-shaped with an average length of 1.95 µm and average width of 0.46 µm. The three isolates shared identical 16S rRNA sequences, displayed 99.72% identity with the sequence from A. xylosoxidans strain SeqID2 (GenBank accession NO. MH266081.1). The glutamate synthase (gltB), GTP-binding membrane protein (lepA), NADH:ubiquinone oxidoreductase subunit L (nuoL), RNA polymerase beta-subunit (rpoB), and the enolase (eno) genes of the three isolates were amplified by PCR using primer pairs gltB-F/gltB-R, lepA-F/lepA-R, nuoL-F/nuoL-R, rpoB-F/rpoB-R and eno-F/eno-R, respectively (Spilker et al. 2012; Vandamme et al. 2016). The gene sequences of 16S rRNA (OQ711945, OQ740153 and OR230037), gltB (OR242732, OQ737692 and OR262112), lepA (OR233727, OQ737693 and OR262113), nuoL (OR233726, OQ737694 and OR262114), ropB (OR233725, OQ737695 and OR262115) and eno (OR242733, OQ737696 and OR262116) for the isolates ZOR02, ZOR05 and ZOR12 were deposited in GenBank database. The gltB, lepA, nuoL, rpoB and eno sequences of the isolates ZOR02, ZOR05 and ZOR12 showed 98.66-99.16%, 98.9-100%, 96.28%-97.34%, 98.47-99.44% and 99.27-99.82% similarity to A. xylosoxidans strain AX27, respectively. Phylogenetic trees were constructed based on the 16S rRNA and gltB-lepA-nuoL-rpoB-eno multilocus using the Neighbor-Joining (NJ) method with 1000 bootstrap replicates in MEGA11.0 software (Álvarez et al. 2018). For pathogenicity tests, bacterial suspensions were initially prepared in sterile water at a final concentration of 108 CFU mL-1. Subsequently, 10 μL of bacterial suspensions was injected into the stem base of two-month-old ginger plants, while sterile water was used as a control (Wang et al. 2022). These plants were then incubated at 28°C and 70% relative humidity. There were three replicates for each treatment, and each replicate contained five plants. After six days of inoculation, the ginger plants injected with bacterial suspensions alone exhibited severe wilting symptoms similar to those observed in the field. However, water-soaked symptoms were not observed on rhizome tissues from the pathogen-infected plants. Bacterial pathogens were re-isolated from the diseased plants and identified using the morphological and molecular methods to meet Koch's hypothetical tests. To our knowledge, this is the first report of A. xylosoxidans causing wilt disease of ginger in China. In 2022, the average yield loss due to wilt disease in the Yi'an District of Tongling exceeded 20%, posing a major threat to local ginger cultivation. Effective disease management strategies are needed to develop for the control and prevention of the disease.
生姜(Zingiber officinale)是一种重要的经济作物,在中国已广泛种植了2500多年。其中一个品种,铜陵白姜,种植于中国安徽省铜陵市义安区(北纬30°45′,东经117°43′)。2022年8月,生姜植株上出现了黄化和萎蔫症状,田间发病率超过20%。患病植株的茎基部变软、褐色且呈水渍状。此外,根茎表现出褐变和水渍状腐烂症状,类似于由青枯雷尔氏菌(Ralstonia solanacearum)和阴沟肠杆菌(Enterobacter cloacae)引起的症状(Yu等人,2003年;Nishijima等人,2004年;Liu等人,2021年)。因此,生姜青枯病可能是由多种病原菌感染共同导致的。为了鉴定引起青枯病的新病原菌,将来自不同地点的患病植株的茎组织用1%次氯酸钠(NaOCl)消毒10分钟,然后用无菌水冲洗至少三次。消毒后的样品用0.9%生理盐水研磨,并在室温下放置30分钟。取20 μL悬浮液进行系列稀释,并在28°C的Luria-Bertani(LB)培养基上培养。共挑选并纯化了217个分离株,通过使用引物27F/1492R进行16S rRNA基因分析进行分类鉴定(Weisburg等人,1991年)。在这些分离株中,通过NCBI BLASTn分析鉴定出23个单菌落分离株为木糖氧化无色杆菌(A. xylosoxidans)。此外,从不同地点随机选择了三个单分离株进行进一步实验。生长的菌落呈不透明白色且圆形。显微镜观察显示,细胞呈杆状,平均长度为1.95 µm,平均宽度为0.46 µm。这三个分离株的16S rRNA序列相同,与木糖氧化无色杆菌菌株SeqID2(GenBank登录号:MH266081.1)的序列相似度为99.72%。使用引物对gltB-F/gltB-R、lepA-F/lepA-R、nuoL-F/nuoL-R、rpoB-F/rpoB-R和eno-F/eno-R,通过PCR分别扩增这三个分离株的谷氨酸合酶(gltB)、GTP结合膜蛋白(lepA)、NADH:泛醌氧化还原酶亚基L(nuoL)、RNA聚合酶β亚基(rpoB)和烯醇酶(eno)基因(Spilker等人,2012年;Vandamme等人,2016年)。分离株ZOR02、ZOR05和ZOR12的16S rRNA(OQ711945、OQ740153和OR230037)、gltB(OR242732、OQ737692和OR262112)、lepA(OR233727、OQ737693和OR262113)、nuoL(OR233726、OQ737694和OR262114)、ropB(OR233725、OQ737695和OR262115)和eno(OR242733、OQ737696和OR262116)的基因序列已存入GenBank数据库。分离株ZOR02、ZOR05和ZOR12的gltB、lepA、nuoL、rpoB和eno序列与木糖氧化无色杆菌菌株AX27的相似度分别为98.66 - 99.16%、98.9 - 100%、96.28% - 97.34%、98.47 - 99.44%和99.27 - 99.82%。使用MEGA11.0软件中的邻接法(NJ),基于16S rRNA和gltB - lepA - nuoL - rpoB - eno多位点构建系统发育树,并进行1000次重复抽样(Álvarez等人,2018年)。对于致病性测试,首先在无菌水中制备最终浓度为108 CFU mL-1的细菌悬浮液。随后,将10 μL细菌悬浮液注射到两个月大的生姜植株的茎基部,同时用无菌水作为对照(Wang等人,2022年)。然后将这些植株在28°C和70%相对湿度下培养。每个处理有三个重复,每个重复包含五株植物。接种六天后,仅注射细菌悬浮液的生姜植株表现出与田间观察到的严重萎蔫症状相似的症状。然而,在病原菌感染植株的根茎组织上未观察到水渍状症状。从患病植株中重新分离出细菌病原体,并使用形态学和分子方法进行鉴定,以满足科赫假设检验。据我们所知, 这是木糖氧化无色杆菌在中国引起生姜青枯病的首次报道。2022年,铜陵义安区因青枯病造成的平均产量损失超过20%,对当地生姜种植构成了重大威胁。需要制定有效的病害管理策略来控制和预防该病。