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与印度马齿苋小叶病相关的三叶草增殖(16SrVI)组植原体的发生情况

Occurrence of a Clover Proliferation (16SrVI) Group Phytoplasma Associated with Little Leaf Disease of Portulaca grandiflora in India.

作者信息

Samad A, Ajayakumar P V, Shasany A K, Gupta Mahesh K, Alam M, Rastogi S

机构信息

Central Institute of Medicinal and Aromatic Plants (CIMAP), P.O. CIMAP, Lucknow 226015, India.

出版信息

Plant Dis. 2008 May;92(5):832. doi: 10.1094/PDIS-92-5-0832A.

Abstract

Portulaca grandiflora (family Portulacaceae), commonly known as moss rose purslane, is a popular ornamental plant widely grown in temperate climates because it blooms all summer. Portulaca is also used for medicinal purposes since it is rich in vitamins A, B1, and C and has antimicrobial and cytotoxic activity. Since March 2005, 30 to 50% of P. grandiflora plants in the ornamental gardens as well as in pots at the Central Institute of Medicinal and Aromatic Plants, Lucknow, India have displayed symptoms resembling phytoplasma infection. Disease symptoms start as a typical bud proliferation, downward curling, and diminishing size of leaves, followed by overall stunted growth and yellowing of the whole plant from April to June. Some plants also formed rosettes and a proliferation of axillary shoots resulting in a witches'-broom appearance. Typical pleomorphic bodies, mostly spherical to oval, ranging from 340 to 1,100 nm were observed only in sieve elements of infected plants by transmission electron microscopy (TEM). On the basis of symptoms, TEM observations, PCR, and response to antibiotic treatment, the causal organism was identified as phytoplasma (1). Total genomic DNA from healthy and infected plants was extracted with the CTAB buffer method (2). Of 27 suspected samples screened by PCR, 23 were phytoplasma positive. Presence of phytoplasmas in plants was demonstrated by a nested PCR assay employing primer pair P1/P6 followed by R16F2n/R16R2 that generated rDNA products of 1.5 and 1.2 kb, respectively, only from symptomatic plants. No differences among phytoplasmas in Portulaca plants were detected by restriction fragment length polymorphism (RFLP) analysis of nested rDNA (1.2 kb) products using endonucleases BamHI, RsaI, AluI, HpaII, and EcoRI. Comparative analysis of RFLP patterns with those derived from reference phytoplasmas tentatively identified the Portulaca little leaf (PLL) phytoplasma as a member of 16S rDNA RFLP group 16SrVI (3). A nested PCR product (1.25 kb) was cloned with a TOPO TA cloning kit (Invitrogen, Carlsbad, CA) and sequenced. The sequence was deposited in the GenBank database (Accession No. EF651786). Sequence analysis revealed the PLL phytoplasma to be most similar (98%) to Indian brinjal little leaf (Accession No. EF186820) and 'Candidatus Phytoplasma trifolii' (Accession No. AY390261), two 16SrVI group phytoplasmas previously reported from India and Canada, respectively. The status of PLL (EF651786) was also verified by in silico RFLP analysis (4) of the F2n/R2 sequence of six closely related strains (Accession Nos. AF228052, AY390261, AY270156, AY409070, AY409069, and EF186820) of the 16SrVI group using 17 restriction enzymes (AluI, BamHI, BfaI, BsfUI, DraI, EcoRI, HaeIII, HhaI, HinfI, HpaI, HpaII, KpnI, MseI, Sau3AI, RsaI, SspI, and TaqI). In silico restriction digestion and virtual gel plotting showed similar patterns for all enzymes. To our knowledge, this is the first report of a 16SrVI group phytoplasma infecting Portulaca plants in India. References: (1) P. V. Ajayakumar et al. Aust. Plant Dis. Notes 2:67, 2007. (2) S. P. S. Khanuja et al. Plant Mol. Biol. Rep. 17:74, 1999. (3) I.-M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998. (4) W. Wei et al. Int. J. Syst. Evol. Mic. 57:1855, 2007.

摘要

大花马齿苋(马齿苋科),俗称松叶牡丹,是一种广受欢迎的观赏植物,因其整个夏季都能开花,所以在温带气候地区广泛种植。马齿苋还具有药用价值,因为它富含维生素A、B1和C,并且具有抗菌和细胞毒性活性。自2005年3月以来,印度勒克瑙中央药用和芳香植物研究所的观赏花园以及花盆中的大花马齿苋植株,有30%至50%出现了类似植原体感染的症状。病害症状始于典型的芽增殖、叶片向下卷曲和变小,随后在4月至6月期间整株植物生长发育受阻并变黄。一些植株还形成了莲座状以及腋芽增殖,导致呈现出扫帚状外观。通过透射电子显微镜(TEM)观察,仅在受感染植株的筛管分子中观察到典型的多形性菌体,大多为球形至椭圆形,大小在340至1100纳米之间。基于症状、TEM观察、PCR以及对抗生素处理的反应,确定致病生物为植原体(1)。采用CTAB缓冲液法(2)从健康植株和受感染植株中提取总基因组DNA。在通过PCR筛选的27个疑似样本中,23个为植原体阳性。仅从有症状的植株中,通过使用引物对P1/P6随后是R16F2n/R16R2的巢式PCR检测,分别产生了1.5千碱基和1.2千碱基的rDNA产物,证明植株中存在植原体。使用核酸内切酶BamHI、RsaI、AluI、HpaII和EcoRI对巢式rDNA(1.2千碱基)产物进行限制性片段长度多态性(RFLP)分析,未检测到马齿苋植株中植原体之间的差异。将RFLP模式与参考植原体的模式进行比较分析,初步确定马齿苋小叶(PLL)植原体为16S rDNA RFLP组16SrVI的成员(3)。使用TOPO TA克隆试剂盒(Invitrogen,加利福尼亚州卡尔斯巴德)克隆了一个巢式PCR产物(1.25千碱基)并进行测序。该序列已存入GenBank数据库(登录号EF651786)。序列分析表明,PLL植原体与印度茄子小叶(登录号EF186820)和“三叶草韧皮部杆菌”(登录号AY390261)最为相似(98%),这两种16SrVI组植原体此前分别在印度和加拿大被报道过。还通过对16SrVI组六个密切相关菌株(登录号AF228052、AY390261、AY270156、AY409070、AY409069和EF186820)的F2n/R2序列进行电子RFLP分析(4),使用17种限制性酶(AluI、BamHI、BfaI、BsfUI、Dral、EcoRI、HaeIII、HhaI、HinfI、HpaI、HpaII、KpnI、MseI、Sau3AI、RsaI、SspI和TaqI)验证了PLL(EF651786)的分类地位。电子限制性酶切和虚拟凝胶图谱显示所有酶的模式相似。据我们所知,这是印度关于16SrVI组植原体感染马齿苋植株的首次报道。参考文献:(1)P. V. Ajayakumar等人,《澳大利亚植物病害记录》2:67,2007年。(2)S. P. S. Khanuja等人,《植物分子生物学报告》17:74,1999年。(3)I.-M. Lee等人,《国际系统细菌学杂志》48:1153,1998年。(4)W. Wei等人,《国际系统与进化微生物学杂志》57:1855,2007年。

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