Biswas C, Dey P, Mandal K, Mitra J, Satpathy S, Karmakar P G
Central Research Institute for Jute and Allied Fibres (CRIJAF), Barrackpore, Kolkata, West Bengal 700120, India.
Plant Dis. 2014 Sep;98(9):1267. doi: 10.1094/PDIS-02-14-0147-PDN.
Flax or linseed is grown as a fiber or oilseed crop in tropical and temperate regions. It is commercially cultivated in many countries of the world including Canada, China, India, the United States, Ethiopia, Pakistan, Russia, Poland, and Argentina (1). In December 2013, symptoms suggestive of phytoplasma infection were noticed on flax in different experimental fields of Central Research Institute for Jute and Allied Fibres (CRIJAF) research farm, Barrackpore, India, and the incidence was less than 2%. Because incidence of phytoplasma diseases are increasing worldwide, occurrence of a phytoplasma in a new geographical area poses an imminent threat. The infected plants showed floral virescence, phyllody, and stem fasciation (flattened stem). Floral malformation was very conspicuous with abnormal structures replacing normal flowers. All the floral parts, including petals, turned into green leaves. Total DNA was extracted from leaf mid veins of three symptomatic and three asymptomatic plants using a DNeasy Plant Mini Kit (Qiagen). PCR was carried out with the phytoplasma-specific universal P1/P7 primer set followed by nested primer pair R16F2n/R16R2 (2), resulting in DNA amplicons that were 1.8 kb and 1.2 kb, respectively, in all symptomatic samples tested. No amplification was observed with DNA from symptomless samples. This suggested association of a phytoplasma with the disease. The five purified nested PCR products were cloned in a pGEM-T Easy vector (Promega) and sequenced. One of the sequences that proved to be identical to the others was deposited in GenBank (Accession No. KJ417660). The consensus sequence was analyzed by NCBI BLAST and found to share 99% similarity with the 16Sr DNA sequence of the 'Candidatus Phytoplasma asteris' reference strain (GenBank HQ828108), which belongs to 16SrI group. The phylogenetic tree based on 16SrDNA sequence of phytoplasmas belonging to group 16SrI and other distinct phytoplasma groups also showed that the phytoplasma clustered with members of group 16SrI (3). The nested PCR product of R16F2n/R16R2 was digested using restriction enzymes AluI, BfaI, BstU, HhaI, HpaI, KpnI, MseI, and RsaI. The RFLP patterns were compared with those of known phytoplasma strains (2) and they matched the patterns for aster yellows subgroup B (16Sr I-B). Subsequently, the iPhyClassifier 16Sr group/subgroup classification based on similarity (4) analyses showed that the studied strain had 16SrDNA sequences in the 16SrI-B group with a similarity coefficient of 1.00. To the best of our knowledge, this is the first report of 16SrI-B phytoplasma associated with flax in India. References: (1) K. P. Akhtar et al. Phytoparasitica 41:383, 2013. (2) I. M. Lee et al. Int. J. Syst. Evol. Microbiol. 54:337, 2004. (3) N. Saitou and M. Nei. Mol. Biol. Evol. 4:406, 1987. (4) Y. Zhao et al. Int. J. Syst. Evol. Microbiol. 59:2582, 2009.
亚麻在热带和温带地区作为纤维作物或油料作物种植。它在世界许多国家都有商业化种植,包括加拿大、中国、印度、美国、埃塞俄比亚、巴基斯坦、俄罗斯、波兰和阿根廷(1)。2013年12月,在印度巴拉克布尔黄麻及相关纤维中央研究所(CRIJAF)研究农场的不同试验田中,亚麻上出现了疑似植原体感染的症状,发病率低于2%。由于植原体病害在全球范围内呈上升趋势,在新的地理区域出现植原体构成了紧迫威胁。受感染的植株表现出花变绿、叶变花以及茎扁化(茎扁平)。花畸形非常明显,异常结构取代了正常花朵。所有花的部分,包括花瓣,都变成了绿叶。使用DNeasy植物微量提取试剂盒(Qiagen)从三株有症状和三株无症状植株的叶片中脉提取总DNA。用植原体特异性通用引物对P1/P7进行PCR,随后用巢式引物对R16F2n/R16R2进行PCR(2),在所有检测的有症状样本中分别产生了1.8 kb和1.2 kb的DNA扩增子。无症状样本的DNA未观察到扩增。这表明植原体与该病害有关。将五个纯化的巢式PCR产物克隆到pGEM-T Easy载体(Promega)中并进行测序。其中一个与其他序列相同的序列存入了GenBank(登录号KJ417660)。通过NCBI BLAST对共有序列进行分析,发现其与‘Candidatus Phytoplasma asteris’参考菌株(GenBank HQ828108)的16Sr DNA序列相似度为99%,该参考菌株属于第16SrI组。基于属于16SrI组的植原体和其他不同植原体组的16SrDNA序列构建的系统发育树也表明,该植原体与16SrI组的成员聚类在一起(3)。用限制性内切酶AluI、BfaI、BstU、HhaI、HpaI、KpnI、MseI和RsaI对R16F2n/R16R2的巢式PCR产物进行消化。将限制性片段长度多态性(RFLP)模式与已知植原体菌株的模式进行比较(2),它们与翠菊黄化亚组B(16Sr I - B)的模式匹配。随后,基于相似性的iPhyClassifier 16Sr组/亚组分类(4)分析表明,所研究的菌株在16SrI - B组中有16SrDNA序列,相似系数为1.00。据我们所知,这是印度首次报道与亚麻相关的16SrI - B植原体。参考文献:(1)K. P. Akhtar等人,《植物寄生》41:383,2013年。(2)I. M. Lee等人,《国际系统与进化微生物学杂志》54:337,2004年。(3)N. Saitou和M. Nei,《分子生物学与进化》4:406,1987年。(4)Y. Zhao等人,《国际系统与进化微生物学杂志》5:2 :582,2009年。