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Ahmed Nasim Zaidi Syed Shan-e-Ali Amin Imran Scheffler Brian E. Mansoor Shahid 《European journal of plant pathology / European Foundation for Plant Pathology》2021,160(2):249-257
European Journal of Plant Pathology - The ongoing global spread of Tomato yellow leaf curl virus (TYLCV) poses an endemic threat to tomato production in all tropical and sub-tropical regions of the... 相似文献
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First report of cotton leaf curl disease affecting chili peppers 总被引:2,自引:0,他引:2
M. Hussain S. Mansoor I. Amin S. Iram Y. Zafar K. A. Malik R. W. Briddon 《Plant pathology》2003,52(6):809-809
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Virus isolates GD6, GD7, GD8, GD9 and GD10 were obtained from Malvastrum coromandelianum showing leaf curl symptoms in Guangdong Province of China. A specific 500 bp product was consistently detected in total DNA extracts, amplified with universal primers specific for members of the genus Begomovirus. Analysis of their partial DNA sequences revealed that they are isolates of the same begomovirus species, sharing 92·8%–97·1% nucleotide sequence identity. The complete DNA sequences of both GD6 and GD9 were found to be 2767 nucleotides, with all the characteristic features of begomovirus genome organization. The two isolates have less than 85·2% nucleotide sequence identity with other reported begomoviruses. Consequently, GD6 and GD9 are considered to be isolates of a novel begomovirus species, for which the name Malvastrum leaf curl Guangdong virus (MLCuGdV) is proposed. Sequence analyses suggest that MLCuGdV may have arisen by recombination between viruses related to Papaya leaf curl China virus , Tomato leaf curl Philippines virus and other undiscovered virus ancestors. Neither the DNA-B component nor the DNAβ molecule associated with these begomovirus isolates was found. An infectious clone of GD6 was constructed. GD6 efficiently infected Nicotiana benthamiana , N. glutinosa and Petunia hybrida by agro-inoculation, and Malvastrum coromandelianum by whitefly transmission, inducing leaf curling, vein swelling and stunting symptoms. GD6 was also infectious in N. tabacum , but did not induce observable disease symptoms. 相似文献
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Youping Xu Xinzhong Cai Xueping Zhou 《European journal of plant pathology / European Foundation for Plant Pathology》2007,118(3):287-294
Three begomovirus isolates were obtained from tomato plants showing leaf curl symptoms in Guangxi province of China. Typical
begomovirus DNA components representing the three isolates (GX-1, GX-2 and GX-3) were cloned and their full-length sequences
were determined to be 2752 nucleotides. Nucleotide identities among the three viral sequences were 98.9–99.7%, but all shared
<86.7% nucleotide sequence identity with other reported begomoviruses. The sequence data indicated that GX-1, GX-2 and GX-3
are isolates of a distinct begomovirus species for which the name Tomato leaf curl Guangxi virus (ToLCGXV) is proposed. Further
analysis indicated that ToLCGXV probably originated through recombination among viruses related to Ageratum yellow vein virus,
Tomato leaf curl China virus and Euphorbia leaf curl virus. PCR and Southern blot analyses demonstrated that isolates GX-1
and GX-2 were associated with DNAβ components, but not isolate GX-3. Sequence comparisons revealed that GX-1 and GX-2 DNAβ
components shared the highest sequence identity (86.2%) with that of Tomato yellow leaf curl China virus (TYLCCNV). An infectious
construct of ToLCGXV isolate GX-1 (ToLCGXV-GX) was produced and determined to be highly infectious in Nicotiana benthamiana, N. glutinosa, tobacco cvs. Samsun and Xanthi, tomato and Petunia hybrida plants inducing leaf curl and stunting symptoms. Co-inoculation of tomato plants with ToLCGXV-GX and TYLCCNV DNAβ resulted
in disease symptoms similar to that caused by ToLCGXV-GX alone or that observed in infected field tomato plants. 相似文献
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S. Mansoor I. Amin S. Iram M. Hussain Y. Zafar K. A. Malik R. W. Briddon 《Plant pathology》2003,52(6):784-784
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为明确南疆温室番茄黄化曲叶病的病毒种类,利用双生病毒的兼并引物通过PCR扩增,对采集的20个番茄病株进行了分子检测.从20个病株中均扩增到约500 bp的目标片段,对其中4株进行克隆和测序,其相互间序列同源性为97.1% ~99.3%,与番茄黄化曲叶病毒(Tomato yellow leaf curl virus,TYLCV)的同源性较高,为98.6% ~ 99.5%.随机选取莎车分离物KS2-5进行全基因组的克隆和测序,KS2-5 DNA全长为2781 nt(序列号:JQ807735),具有典型的双生病毒基因组特征,与TYLCV其它分离物同源性达到98.9%~99.5%,而与其它粉虱传双生病毒的序列同源性较低,为68.3% ~75.5%,表明危害南疆温室番茄的病毒种类为番茄黄化曲叶病毒TYLCV. 相似文献
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