Voronina Maya V, Lukianova Anna A, Shneider Mikhail M, Korzhenkov Aleksei A, Toschakov Stepan V, Miroshnikov Kostantin A, Vasiliev Dmitri M, Ignatov Aleksandr
PhytoEngineering R&D Center, Moscow, Russian Federation;
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry Russian Academy of Sciences, 68485, Molecular bioengineering, Moscow, Moscow, Russian Federation;
Plant Dis. 2021 Jan 26. doi: 10.1094/PDIS-09-20-1864-PDN.
Blackleg and soft rot of potato (Solanum tuberosum) were monitored in the Central European part of Russia within a period of 2012- 2019. Symptoms included decay of tubers, blackening of stem vascular bundles, and partial yellowing of leaves. The disease causes serious potato yield losses in the field and storage. Pectobacterium parmentieri, P. brasiliense, P. versatile (syn. Ca. Pectobacterium maceratum), P. carotovorum, P. atrosepticum, Dickeya dianthicola, and D. solani are considered as main causal agents of soft rot and blackleg disease in Russia (Voronina et al. 2019, Ngoc Ha et al., 2019, Shirshikov et al. 2018, Kornev et al. 2012). Potato plant samples collected in commercial fields in routine plant health assay were used for bacteria isolation on crystal violet pectate agar (CVP) (Helias et al. 2012) as described previously (Voronina et al. 2019). Bacterial colonies producing pitting on CVP were re-isolated and purified on nutrient broth yeast extract medium. DNA of bacterial isolates was extracted, and polymerase chain reaction (PCR) amplifications were performed using gapA primers (Cigna et al. 2017) followed by sequencing. DNA sequence alignment showed that the isolates F099, F100, F106, F109, and F118 were identical (deposited as part of NCBI Ref.Seq. for F109 NZ_RRYS01000004.1, locus KHDHEBDM_RS06360) and grouped together with the type strain Pectobacterium polaris NIBIO1006T (CP017481), a new species described as a potato pathogen (Dees et al. 2017). These strains were negative in diagnostic PCR assays using specific primers Y45/Y46 for the detection of P. atrosepticum, Br1f and L1r for P. brasiliense (Duarte et al. 2004), and ADE1/ADE2 for Dickeya sp. (Nassar et al. 1996). To further validate the identification, strain F109 of P. polaris was selected for genome sequencing. The genome of P. polaris strain F109, (NCBI Reference Sequence NZ_RRYS00000000.1) reveals >99% sequence similarity with type strain P. polaris IPO_1606 (GenBank accession GCA_902143345.1). The strain F109 was deposited to All-Russian Collection of Microorganisms under number VKM V-3420. Thus, the characterization of five isolates provided evidence that a previously unreported pathogen was present in the surveyed fields. The isolates were uniform in genetic and physiological properties; they were gram negative, facultative anaerobes with pectinolytic activity, negative for oxidase, urease, indole production, gelatin liquefaction. All isolates were catalase positive, produced acid from lactose, rhamnose, saccharose, xylose, and trehalose, and were tolerant to 5% NaCl, unable to utilize malonate and citrate. All the isolates grew at 37°C. All isolates caused soft rot symptoms on 10 inoculated potato tubers. They produced typical black leg rot symptoms in young potato plants inoculated with 107 CFU/ml of the pathogen by stem injection and incubated at 25°C for 48 h. The bacteria were re-isolated successfully from symptomatic potato and pathogen confirmed by gapA sequencing to complete Koch's postulates. To our knowledge, this is the first report of blackleg and soft rot caused by P. polaris on potato in the Russian Federation. According to the data of commercial diagnostic laboratory "PhytoEngineering" (Moscow region), P. polaris occurred in 5% potato seed stocks harvested in 2017-2019 in the Moscow region. This finding may indicate that new Pectobacterium strains have adapted to a diverse environment, which is consistent with widespread distribution of commercial seed potatoes. The author(s) declare no conflict of interest. Funding: This work was supported by Russian Science Foundation grant #16-16-00073.
2012年至2019年期间,对俄罗斯中欧部分地区马铃薯(Solanum tuberosum)的黑胫病和软腐病进行了监测。症状包括块茎腐烂、茎维管束变黑以及叶片部分发黄。该病在田间和储存过程中会导致马铃薯严重减产。在俄罗斯,Pectobacterium parmentieri、P. brasiliense、P. versatile(同义词:Ca. Pectobacterium maceratum)、P. carotovorum、P. atrosepticum、Dickeya dianthicola和D. solani被认为是软腐病和黑胫病的主要致病因子(Voronina等人,2019年;Ngoc Ha等人,2019年;Shirshikov等人,2018年;Kornev等人,2012年)。在常规植物健康检测中,从商业田地采集的马铃薯植株样本用于在结晶紫果胶酸盐琼脂(CVP)上进行细菌分离(Helias等人,2012年),方法如先前所述(Voronina等人,2019年)。在CVP上产生蚀斑的细菌菌落被重新分离,并在营养肉汤酵母提取物培养基上纯化。提取细菌分离株的DNA,并使用gapA引物进行聚合酶链反应(PCR)扩增(Cigna等人,2017年),随后进行测序。DNA序列比对显示,分离株F099、F100、F106、F109和F118是相同的(作为F109的NCBI Ref.Seq.的一部分保存,NZ_RRYS01000004.1,基因座KHDHEBDM_RS06360),并与极地果胶杆菌模式菌株NIBIO1006T(CP017481)归为一类,极地果胶杆菌是一种被描述为马铃薯病原体的新物种(Dees等人,2017年)。在使用用于检测P. atrosepticum的特异性引物Y45/Y46、用于检测P. brasiliense的Br1f和L1r(Duarte等人,2004年)以及用于检测Dickeya sp.的ADE1/ADE2(Nassar等人,1996年)的诊断PCR检测中,这些菌株均为阴性。为了进一步验证鉴定结果,选择极地果胶杆菌菌株F109进行基因组测序。极地果胶杆菌菌株F109的基因组(NCBI参考序列NZ_RRYS00000000.1)与模式菌株极地果胶杆菌IPO_1606(GenBank登录号GCA_902143345.1)的序列相似性>99%。菌株F109以编号VKM V - 3420保藏于全俄微生物保藏中心。因此,对五个分离株的鉴定表明,在所调查的田地中存在一种先前未报道的病原体。这些分离株在遗传和生理特性上是一致的;它们是革兰氏阴性兼性厌氧菌,具有果胶分解活性,氧化酶、脲酶、吲哚产生、明胶液化检测均为阴性。所有分离株过氧化氢酶阳性,能从乳糖、鼠李糖、蔗糖、木糖和海藻糖产酸,耐受5% NaCl,不能利用丙二酸和柠檬酸盐。所有分离株在37°C下生长。所有分离株对接种的10个马铃薯块茎均引起软腐症状。通过茎注射接种107 CFU/ml病原体并在25°C下培养48小时后,它们在幼嫩马铃薯植株中产生典型的黑胫腐烂症状。从有症状的马铃薯中成功重新分离出细菌,并通过gapA测序确认病原体,从而完成了科赫法则。据我们所知,这是俄罗斯联邦首次关于极地果胶杆菌引起马铃薯黑胫病和软腐病的报道。根据商业诊断实验室“植物工程学”(莫斯科地区)的数据,2017 - 2019年在莫斯科地区收获的5%马铃薯种薯中存在极地果胶杆菌。这一发现可能表明新的果胶杆菌菌株已经适应了多样化的环境,这与商业种薯的广泛分布是一致的。作者声明无利益冲突。资助:本研究得到俄罗斯科学基金会资助项目#16 - 16 - 00073的支持。