- Open Access
Infectious clones of Tomato leaf curl Palampur virus with a defective DNA B and their pseudo-recombination with Tomato leaf curl New Delhi virus
© Malik et al; licensee BioMed Central Ltd. 2011
Received: 3 January 2011
Accepted: 15 April 2011
Published: 15 April 2011
Tomato leaf curl Palampur virus (ToLCPMV) is a bipartite begomovirus which has been reported from India and Iran but infectious clones have not been obtained. We have previously shown the association of Zucchini yellow mosaic virus (ZYMV), a potyvirus, with severe leaf curl disease of muskmelon in Pakistan. However, the severity of symptoms in the field and yield losses led us to believe that some other agent, such as a begomovirus, could be associated with the disease.
A bipartite begomovirus associated with a severe yellow leaf curl disease on muskmelon in Pakistan has been characterized. Analysis of the complete nucleotide sequence of the DNA A and DNA B components of the begomovirus showed that it has the highest DNA sequence identity with ToLCPMV. However, the gene encoding the nuclear shuttle protein (NSP) was truncated in comparison to previously characterised isolates. Agrobacterium-mediated inoculation of Nicotiana benthamiana with the ToLCPMV clones obtained here did not result in symptoms. However, inoculation of plants with the DNA A component of ToLCPMV and the DNA B component of Tomato leaf curl New Delhi virus (ToLCNDV) lead to systemic infection with leaf curl symptoms. This suggested that the lack of infectivity of the ToLCPMV clones was due to the defect in DNA B. The DNA B of ToLCPMV was able to move systemically when inoculated with DNA A of the either virus. Agro-infiltration of muskmelon with the DNA A and DNA B components of ToLCPMV did not lead to symptomatic infection whereas inoculation with the DNA A with the DNA B of ToLCNDV resulted in a hypersensitive response (HR) along the veins. Additionally, agro-infiltration of muskmelon with a construct for the expression of the NSP gene of ToLCNDV under the control of the cauliflower mosaic virus 35S promoter induced a HR, suggesting that this is the gene causing the HR.
Both ToLCPMV and ZYMV are associated with muskmelon leaf curl disease in Pakistan. However, the ToLCPMV variant identified in association with ZYMV has a defective NSP. The results suggest that a variant with a defective NSP may have been selected for in muskmelon, as this protein is an avirulence determinant in this species, and possibly that infection requires the synergistic interaction with ZYMV.
Whitefly-transmitted geminiviruses have emerged as major pathogens of food and fiber crops throughout the world, particularly in tropical and sub-tropical regions . Viruses of the family Geminiviridae have circular single-stranded (ss) DNA genomes, encapsidated in characteristic twinned isometric particles. These viruses are classified into four genera, Mastrevirus, Curtovirus, Topocuvirus and Begomovirus  depending upon their insect vector, host range and genome organization. Begomoviruses are exclusively transmitted by the whitefly Bemisia tabaci and infect only dicotyledonous plants. They may be monopartite or bipartite (having genomes consisting of one or two circular single-stranded DNA molecules) . Since the identification of the betasatellites , it has become apparent that the majority of begomoviruses in the Old World are monopartite and associate with betasatellites, asymptom modulating ssDNA satellite [5–7].
Several factors, including multiple infections, recombination and interspecific synergism, appear to be the major cause of the increased importance of begomoviruses to agriculture in recent years. Intriguingly, begomovirus-betasatellite complexes do not appear to be a problem in cucurbits; only a single defective betasatellite isolated from a cucurbit has been reported so far . The DNA A and DNA B components of begomoviruses encode genes both in the virion and complementary-sense orientations. Old World begomoviruses encode four open reading frames (ORFs) in the complementary-sense that are involved in viral DNA replication and control of gene expression, while two ORFs in the virion-sense are involved in virus encapsidation and movement. The two proteins encoded by the DNA B component are the nuclear shuttle protein (NSP) and the movement protein (MP) that are involved in nuclear transport and cell-to-cell movement of viral DNA, respectively .
Both watermelon and muskmelon form an important part of diet in Pakistan, particularly in early summer. These crops fit nicely in the cropping pattern where vegetables are grown in the winter months when land is available before the start of cotton growing season. However, the traditional muskmelon-growing areas have recently been hit by a severe viral disease. We have previously shown that a potyvirus, Zucchini yellow mosaic virus (ZYMV), is associated with the disease of muskmelon . Here, we have characterized a bipartite begomovirus associated with severe leaf curl disease on muskmelon in Pakistan.
Collection of samples and DNA extraction
Detection and cloning of virus components
Primers used to amplify partial and full length genome sequences of begomovirus components.
Expected fragment size (kb)
Sequencing and sequence analysis
The complete nucleotide sequences of clones were determined by dideoxynucleotide chain-termination sequencing using the PCR-based BIG DYE kit (Perkin-Elmer Cetus) and specific internal primers. Sequencing products were resolved commercially (Macrogen, Korea). Sequence information was stored, assembled and analysed using the Lasergene sequence analysis package (DNAStar Inc., Madison, WI, USA) running on an IBM-compatible PC. Phylogenetic analyses were conducted on matrices of aligned sequences using the neighbour-joining and bootstrap options of Phylip (ver. 3.5c) running on an IBM-compatible personal computer. Sequence alignments were produced using CLUSTAL X . Phylogenetic dendrograms were viewed, manipulated and printed using Treeview .
Agroinoculation of cloned DNA
Partial direct repeat constructs for the Agrobacterium-mediated inoculation of the full-length DNA A and DNA B clones were produced in the binary vector pGreen0029 . An approximately 1680 bp fragment of the DNA A and an approximately 823 bp fragment of the DNA B clones were released from the full-length pTZ57/RT clones by digestion with KpnI and BamHI or HindIII and MluI, respectively, and ligated into suitably digested pGreen0029 vector. The resulting pGreen0029 constructs were then linearised using KpnI and HindIII, respectively, and the full-length fragments (release from the pTZ57/RT clones by digestion with KpnI and HindIII, respectively) ligated into these to yield the partial, direct repeat constructs. The production of constructs in the binary vector pBin19 for inoculation of ToLCNDV has been described previously . These binary vector constructs were transformed into Agrobacterium tumefaciens GV1301 and inoculated to plants by infiltration as described previously .
A bipartite begomovirus is associated with severe disease on melon
As described earlier, a very severe yellow leaf curl disease was observed in several districts of central and southern Punjab, including Vehari, Sahiwal and Khanewal, and was shown to be associated with Zucchini yellow mosaic virus (ZYMV) . Total DNA isolated from symptomatic plants was used as template in PCR with universal primers designed for the amplification of the partial sequences of begomovirus DNA A. The amplified product was cloned and sequenced and it showed the highest levels of nucleotide sequence identity to isolates of Tomato leaf curl Palampur virus (ToLCPMV), a bipartite begomovirus. To confirm the bipartite nature of virus from muskmelon, a PCR product encompassing the movement protein (MP) gene of ToLCNDV was used as a specific probe for Southern hybridisation. All the muskmelon samples found positive for DNA A were also found positive for DNA B (results not shown). Samples were similarly examined for the presence of begomoviruses by Southern blot hybridization using the DNA A of ToLCNDV as a general probe for begomoviruses. The probe hybridized with all sixty samples collected from symptomatic plants that were found positive by PCR.
Cloning and complete nucleotide sequence of DNA A
Positions and coding capacities of genes encoded by ToLCPMV DNA A and DNA B
Position of start codon
Position of stop codon
Size (number of nucleotides)
Predicted size of encoded product (kDa)
Cloning and sequence analysis of DNA B
The partial sequences of DNA B obtained were used to design back-to-back primers (TLCVBF and TLCVBR; Table: 1) for the amplification of the full-length DNA B within the sequence of the movement protein (MP) gene. The desired sized fragment (2.7 kb) of DNA B was cloned in pTZ57RT. The clone was fully sequenced and shown to consist of 2724 bp. The DNA B showed 98% nucleotide sequence identity to an isolate of ToLCPMV recorded from India (accession no. AM992534) whereas the identity to the ToLCPMV isolate from Iran was 90% (accession no. FJ660442). Among the DNA B components of ToLCNDV available in the databases the highest levels of identity (82%) were to an isolate from India obtained from pumpkin (accession no. AM286435). In ORFs, NSP showed 99% sequence identity with ToLCPMV (accession no. AM992534) and it ranged from 90-99%. Whereas it was 73.3% identical to ToLCNDV (accession no AY150305). The maximum sequence identity to ToLCPMV isolate originating from India was 99% but to the isolates originating from Iran it was 95%. Overall among ToLCPMV isolates, sequence identity ranged from 92-99%. ToLCPMV MP was 86% identical to MP of ToLCNDV (accession no AY150304). Thus, DNA B might be a recombinant molecule where the MP is derived from DNA B of ToLCNDV while the intergenic region and NSP are derived from yet an unknown virus. The intergenic region of ToLCPMV shows 86% nucleotide sequence identity to Indian isolate (accession no. AM992534) whereas the identity to Iranian isolate is 76% (accession no. FJ660442). NSP has a size of 555 nucleotides (184 amino acids) and it is truncated at the N-terminus, since first 84 amino acids are missing in comparison to the ToLCNDV sequences available in the database (Figure 1B). The MP has a predicted size of 884 bases (294 amino acids) (Table: 2). Non-coding IR sequences of DNA B are distinct from already published sequences. The intergenic regions of DNA A and DNA B show only 38.2% identity but share a 34-bp potential stem-loop forming region (GGCCATTCGTATAATATTACCGAATGGCCGCGGT). This sequence has the conserved nonanucleotide sequence (TAATATTAC). The iterated elements (iterons) were close to a TATA box in the common region and were identified as GGTGTC (Figure 2) being the same as those identified in DNA A of ToLCPMV and ToLCNDV .
Efforts were made to identify a DNA B in muskmelon having no truncation of the NSP gene. Three set of primers were designed in the NSP and non-coding sequences of DNA B of ToLCNDV (Table: 1). None of the primer sets was able to amplify a product of approximately 2.8 kb. The ability of these sets of primers to amplify full-length DNA B was confirmed by the use of these primers on tomato samples infected experimentally with ToLCNDV. All sets of primers amplified products of the expected size. To further rule out the possible presence of other DNA B, phi29 polymerase was used which has the ability to amplify circular molecules. The amplified product was restricted with PstI endonuclease (for which there are two restriction sites in DNA A) yielding two bands of the expected sizes (969 bases and 1786 bases). The DNA B of ToLCPMV has two PstI restriction sites that are separated by 62 bases. The restriction analysis suggested the presence of a single type of DNA B of ToLCPMV and the absence of DNA B of ToLCNDV (results not shown).
Phylogenetic analysis of ToLCPMV DNA A and DNA B
Infectivity of ToLCPMV clones from muskmelon
ToLCPMV DNA A and DNA B were inoculated by biolistic methods. However, biolistic inoculation did not result in typical disease symptoms. PCR with specific primers was used to confirm systemic infection. The results showed the presence of both DNA A and DNA B in systemically infected leaves. This result shows that DNA B of ToLCPMV is capable of movement with ToLCPMV DNA A although the clone was not capable of inducing typical disease symptoms.
ToLCNDV DNA B will support symptomatic infection of ToLCPMV DNA A
Infectivity of ToLCPMV and ToLCNDV clones to N. benthamiana
Infectivity (no. of plants showing symptoms/no. of plants inoculated)
ToLCPMV DNA A + ToLCPMV DNA B
ToLCPMV DNA A + ToLCNDV DNA B
ToLCNDV DNA A + ToLCPMV DNA B
ToLCNDV DNA A + ToLCNDV DNA B
ToLCPMV DNA A
ToLCNDV DNA A
Inoculation of ToLCPMV DNA A with ToLCNDV DNA B induces a hypersensitive response in muskmelon
Phytopathogenic viruses are major constraints to agricultural productivity throughout the world. It is an unfortunate fact that Pakistan, in common with all other countries of southern Asia, is home to members of virtually all taxonomic groups of plant-infecting viruses [26–31] which, at least in part, explains the low agricultural productivity in the country. Prime amongst these viruses are the begomoviruses that have appeared as dominant pathogens on several crops. We show here that muskmelon samples previously found positive for ZYMV are co-infected with a begomovirus.
The complete nucleotide sequence of DNA A of begomoviruses is sufficient for identification and classification of begomoviruses. Viruses that share more than 90% sequence identity are considered as strain of the same virus while DNA sequence identity below 89% is considered as new species . Based on this threshold value, the begomovirus identified in muskmelon is an isolate of ToLCPMV. The high levels of nucleotide sequence similarity, of both DNA A (86%) and DNAB (73%), between ToLCPMV and ToLCNDV indicate that they have a recent common ancestor and that ToLCPMV represents a lineage that has diverged from ToLCNDV. ToLCNDV has frequently been identified in cucurbits [33–38]. However, Koch's postulates for ToLCNDV causing diseases of cucurbits have not been satisfied. ToLCNDV is a cosmopolitan species that occurs throughout southern Asia, having been reported from Pakistan, India, Thailand and Taiwan [39–43]. However, since no efforts were made in these reports to inoculate clones on cucurbits, it is difficult to know whether an RNA virus was co-infecting these cucurbits.
The genome organization of ToLCPMV is the typical of Old World begomoviruses (having an AV2 gene) and phylogenetic analysis (Figure 3) show it and ToLCNDV to be most similar to (to group with) other begomoviruses with their center of diversity and origins lying in southern Asia [39, 14, 40–42, 25]. Recombination contributes to the genetic diversification of geminivirus populations and has been related to the emergence of some serious plant diseases, as discussed earlier [44–48]. The prerequisite for recombination to occur is co-infection of the same cell of a host plant . ToLCPMV DNA A has high levels of sequence identity to ToLCNDV-IN[PK:Kha:Chi:04] (accession number DQ116880) in the virion-sense (including the intergenic region) and to ToLCNDV-IN[IN:ND:AVT1] (AY428769) in the complementary-sense, indicating that this molecule is an intraspecific recombinant. The geminiviruses evolve/adapt by a number of mechanisms. Contrary to expectations, geminiviruses have nucleotide substitution rates that are comparable to those of RNA viruses . Such high substitution rates would not be expected from a virus that utilizes host-encoded DNA polymerases with error correction. Additionally, recombination and component exchange (known as pseudo-recombination) are the major processes of geminivirus evolution [46, 51–54]. A prime example of this is the ongoing pandemic of cassava mosaic disease that originated in northern Uganda, spread across eastern Africa and continues to spread throughout central and western Africa. The severe cassava mosaic disease of the pandemic is attributed to a recombinant strain of East African cassava mosaic virus known as the "Uganda Variant" .
Like the DNA A component, the DNA B component of ToLCPMV is a recombinant. The complementary-sense sequences (containing the MP gene) originate from ToLCNDV (showing the highest sequence identity with isolate ToLCNDV-IN (PK:Isl:T1/8:00; accession no. AY150304) while the intergenic region and virion-sense sequences are derived from an as yet undiscovered (or extinct) virus; having no high sequence similarity to any sequences in the databases. The DNA B of ToLCPMV is a mutant with a truncation of the NSP gene. It is unable to support symptoms development when inoculated to N. benthamiana in the presence of ToLCPMV DNA A. Mutational analysis suggests that the N-terminal sequences of NSP are involved in nuclear localization while C-terminal sequences are required for interaction with the MP . Thus, truncation of ToLCPMV NSP at the N-terminus likely abolished the nuclear localization of the protein resulting in a defective molecule which cannot support infection or the protein is not produced at all since it is prematurely truncated. The NSP of ToLCNDV virus is a pathogenicity determinant where N-terminal sequences of protein are required for pathogenicity . PCR amplification with universal and specific DNA B primers failed to show the presence of an intact DNA B in muskmelon samples, indicating that this defective molecule is the only DNA B present in muskmelon. We propose that truncated DNA B was selected on muskmelon probably because NSP was recognized by host defense system. Thus, DNA B with truncated NSP was maintained on muskmelon. A recent example of a begomovirus associated with resistance breakdown in cotton lacked an intact TrAP, probably to avoid host defense targeting the TrAP .
The integrity of the genomes of bipartite begomoviruses is maintained by them having compatible Rep binding sequences in the CR. Thus, the DNA A-encoded Rep is able to recognize and initiate the replication of both components [57–59, 23]. Iteron sequences are usually species-specific, thus in most cases, the Rep of one virus would not be expected to recognize the iteron sequences of a distinct species [60–62]. The iteron sequences of ToLCNDV have been identified experimentally . ToLCNDV and ToLCPMV have the same Rep binding sites and this likely explains our experimental finding that ToLCPMV DNA A is able to trans-replicate ToLCNDV DNA B and initiate a productive, symptomatic systemic infection of plants. ToLCNDV is a part of viral complex consisting of several DNA As that exchange DNA Bs readily. Here evidence is provided that, in addition to ToLCNDV and Tomato leaf curl Gujarat virus , the complex also encompasses ToLCPMV. This ability to readily form genomic reassortments (pseudo-recombination) is probably an adaptation that gives the virus complex an evolutionary advantage. Since DNA B components are involved in movement in plants [65, 66], and thus host range determination [67–69], the ability to readily interact with distinct DNA B components will undoubtedly allow the viruses of the complex to alter/adapt their host ranges to take advantage of new niches.
For bipartite begomoviruses DNA B is considered as an integral part of the genome (a genomic component), rather than a satellite, due to the presence of the conserved region (CR) which is present in both components. Satellites are defined as molecules which share no significant sequence similarity with their helper viruses but require them for replication and movement in host plant . Although clearly a DNA B, the lack of appreciable sequence similarity between the DNA A and DNA B components of ToLCPMV, with the exception of the iteron sequences and nonanucleotide sequence, means that the ToLCPMV DNA B component could be deemed a satellite. This contention is strengthened by the ability of the DNA A to readily exchange the component, a feature in common with satellites such as DNA betasatellite. Likely, in this case, the ToLCPMV DNA B is maintained as a satellite (although the question remains as to whether the NSP gene is expressed). Possibly then, in muskmelon, the ToLCPMV DNA B is maintained as a poorly-functional satellite which is not required for the infection. A recent analysis of DNA A and DNA B sequences has suggested that the two components differ in their evolution and DNA B may be considered as a satellite . Further investigation will be needed to address this question. A possible explanation is that NSP being a pathogenicity determinant is the target of host defense as has been demonstrated previously . Since all plants where ToLCPMV is found were earlier reported to be infected with ZYMV , there is a possibility that the defect in NSP is complemented by ZYMV. The presence of this defective DNA B in many plants and in geographically distant fields of muskmelon, as well as in various cucurbit species, however, suggests that this molecule may play an important part. A satellite that provides no selective advantage to a virus would be expected to be lost quite rapidly.
The data presented here show that ToLCPMV is widespread in the region that includes Iran, Pakistan and India and therefore an emerging virus on several crops. Unfortunately, the earlier reports have not demonstrated infectivity analysis and therefore, it is not possible to assess whether DNA B cloned from India and Iran was infectious. The role of ToLCPMV in muskmelon leaf curl disease remains to be demonstrated. We suggest that dual infection of a begomovirus with a defective DNA B and ZYMV may be important for disease symptoms. The lack of availability of infectious clones of ZYMV precludes us satisfying Koch's postulates for the disease in muskmelon. Our earlier results showed that mechanical inoculation of sap from infected muskmelon to healthy melon plants developed disease symptoms . However, the possibility that begomovirus was also transmitted by sap inoculation cannot be ruled out. Our results show that ToLCPV is infectious to experimental hosts when inoculated with DNA B of ToLCNDV. Our recent results from cotton show that the begomovirus isolated from resistant cotton lack TrAP . We hypothesized that begomoviruses may adopt to resistant host by truncation of an important gene. The maintenance of the defective DNA B in all field samples suggests a role for DNA B. It therefore appears that a synergistic interaction with ZYMV may have compensated for the defective NSP. We are trying to understand the possible synergistic interaction by cloning of helper component proteinase of ZYMV in a RNA virus vector such as PVX.
AHM was supported by a Ph.D scholarship from the Higher Education Commission (HEC), Government of Pakistan. RWB is employed by the HEC under the "Foreign Faculty Hiring Scheme". This research was in part supported by research grant under the "Pak-USA linkage program".
- Varma A, Malathi VG: Emerging geminivirus problems: a serious threat to crop production. Ann Appl Biol. 2003, 142: 145-164. 10.1111/j.1744-7348.2003.tb00240.x.View ArticleGoogle Scholar
- Fauquet CM, Mayo MA, Maniloff J, Desselberge U, Ball LA: Virus Taxonomy: VIIIth Report of the International Committee on Taxonomy of Viruses". 2005, Elsevier Academic PressGoogle Scholar
- Stanley J, Bisaro DM, Briddon RW, Brown JK, Fauquet CM, Harrison BD, Rybicki EP, Stenger DC: Geminiviridae. Virus Taxonomy VIIIth Report of the ICTV. Edited by: Fauquet CM, Mayo MA, Maniloff J, Desselberger U, Ball LA. 2005, London: Elsevier/Academic Press, 301-326.Google Scholar
- Saunders K, Bedford ID, Briddon RW, Markham PG, Wong SM, Stanley J: A unique virus complex causes Ageratum yellow vein disease. Proc Natl Acad Sci. 2000, 6890-6895. 10.1073/pnas.97.12.6890.Google Scholar
- Mansoor S, Briddon RW, Zafar Y, Stanley J: Geminivirus disease complexes: an emerging threat. Trends Plant Sci. 2003, 8: 128-134. 10.1016/S1360-1385(03)00007-4.View ArticlePubMedGoogle Scholar
- Mansoor S, Zafar Y, Briddon RW: Geminivirus disease complexes: the threat is spreading. Trends in Plant Sci. 2006, 11: 209-212. 10.1016/j.tplants.2006.03.003.View ArticleGoogle Scholar
- Mansoor S, Briddon RW, Fauquet CM: Maintenance of an Old World betasatellite by a New World helper begomovirus and possible rapid adaptation of the betasatellite. J Virol. 2009, 83: 9347-9355. 10.1128/JVI.00795-09.PubMed CentralView ArticlePubMedGoogle Scholar
- Bull SE, Briddon RW, Markham PG: Universal primers for the PCR-mediated amplification of DNA 1: a satellite-like molecule associated with begomovirus-DNA β complexes. Mol Biotechnol. 2003, 23: 83-86. 10.1385/MB:23:1:83.View ArticlePubMedGoogle Scholar
- Noueiry AO, Lucas WJ, Gilbertson RL: Two proteins of a plant DNA virus coordinate nuclear and plasmodesmal transport. Cell. 1994, 76: 925-932. 10.1016/0092-8674(94)90366-2.View ArticlePubMedGoogle Scholar
- Malik AH, Mansoor S, Iram S, Briddon RW, Zafar Y: A severe outbreak of melon yellow mosaic disease caused by zucchini yellow mosaic virus in Punjab province of Pakistan. Plant Pathol. 2006, 55: 285-10.1111/j.1365-3059.2006.01323.x.View ArticleGoogle Scholar
- Doyle JJ, Doyle JL: Isolation of plant DNA from fresh tissue. Focus. 1990, 12: 13-15.Google Scholar
- Briddon RW, Markham PG: Universal primers for the PCR amplification of dicot-infecting geminiviruses. Mol Biotechnol. 1994, 1: 202-205. 10.1007/BF02921559.View ArticlePubMedGoogle Scholar
- Iram S, Amrao L, Mansoor S, Malik AH, Briddon RW, Zafar Y: First report of begomovrius associated with leaf curl disease of Duranta erecta in Pakistan. Plant Pathol. 2005, 54: 260-10.1111/j.1365-3059.2005.01129.x.View ArticleGoogle Scholar
- Padidam M, Beachy RN, Fauquet CM: Classification and identification of geminiviruses using sequence comparisons. J Gen Virol. 1995, 76: 249-263. 10.1099/0022-1317-76-2-249.View ArticlePubMedGoogle Scholar
- Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The Clustal_X windows interface; flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucl Acid Res. 1997, 25: 4876-4882. 10.1093/nar/25.24.4876.View ArticleGoogle Scholar
- Page RDM: TREEVIEW: An application to display phylogenetic trees on personal computers. Comput Appl Biosci. 1996, 12: 357-358.PubMedGoogle Scholar
- Hellens RP, Edwards EA, Leyland NR, Bean S, Mullineaux PM: pGreen: a versatile and flexible binary Ti Vector for Agrobacteruim-mediated plant transformation. Plant Mol Biol. 2000, 42: 819-832. 10.1023/A:1006496308160.View ArticlePubMedGoogle Scholar
- Hussain M, Mansoor S, Iram S, Fatima AN, Zafar Y: The nuclear shuttle protein of Tomato leaf curl New Delhi virus is a pathogenicity determinant. J Virol. 2005, 79: 4434-4439. 10.1128/JVI.79.7.4434-4439.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Kumar Y, Hallan V, Zaidi AA: Molecular characterization of a distinct bipartite begomovirus species infecting tomato in India. Virus Genes. 2008, 37: 425-431. 10.1007/s11262-008-0286-1.View ArticlePubMedGoogle Scholar
- Heydarnejad J, Mozaffari A, Massumi H, Fazeli R, Gray AJA, Meredith S, Lakay F, Shepherd DN, Martin DP, Varsani A: Complete sequences of tomato leaf curl Palampur virus isolates infecting cucurbits in Iran. Arch Virol. 2009, 154: 1015-1018. 10.1007/s00705-009-0389-6.View ArticlePubMedGoogle Scholar
- Laufs J, Schumacher S, Geisler N, Jupin I, Gronenborn B: Identification of the nicking tyrosine of geminivirus Rep protein. FEBS Lett. 1995, 377: 258-262. 10.1016/0014-5793(95)01355-5.View ArticlePubMedGoogle Scholar
- Chatterji A, Beachy RN, Fauquet CM: Expression of the oligomerization domain of the replication associated protein (Rep) of Tomato leaf curl New Delhi virus interferes with DNA accumulation of heterologous geminiviruses. J Bio Chem. 2001, 276: 25631-25638. 10.1074/jbc.M100030200.View ArticleGoogle Scholar
- Shivaprasad PV, Thillaichidambaram P, Balaji V, Veluthambi K: Expression of full-length and truncated Rep genes from Mungbean yellow mosaic virus-Vigna inhibits viral replication in transgenic tobacco. Virus Genes. 2006, 33: 365-374. 10.1007/s11262-006-0077-5.View ArticlePubMedGoogle Scholar
- Fontes EPB, Luckow VA, Hanley-Bowdoin L: A geminivirus replication protein is a sequence-specific DNA binding protein. Plant Cell. 1994, 4: 597-608. 10.1105/tpc.4.5.597.View ArticleGoogle Scholar
- Hussain M, Mansoor S, Iram S, Fatima AN, Zafar Y: The nuclear shuttle protein of Tomato leaf curl New Delhi virus is a pathogenicity determinant. J Gen Virol. 2005, 79: 4434-4439.View ArticleGoogle Scholar
- Mali VR, Rajegore SB: Occurrence of cucumber mosaic virus on banana in India. Plant Dis. 1979, 63: 138-142.Google Scholar
- Naidu RA, Manohar SK, Reddy DVR, Reddy AS: A plant rhabdovirus associated with peanut veinal chlorosis disease in India. Plant Pathol. 1989, 38: 623-626. 10.1111/j.1365-3059.1989.tb01462.x.View ArticleGoogle Scholar
- Ali A, Natsuaki T, Okuda S: Identification and molecular characterization of viruses infecting cucurbits in Pakistan. J Phytopathol. 2004, 152: 677-682. 10.1111/j.1439-0434.2004.00915.x.View ArticleGoogle Scholar
- Raikhy G, Hallan V, Kulshrestha S, Sharma ML, Ram R, Zaidi AA: Molecular characterization of an Indian isolate of Carnation etched ring virus. Acta Virol. 2003, 43: 105-111.Google Scholar
- Varma R, Prakash S, Tomer SPS: First report of Zucchini yellow mosaic virus in cucumber (Cucumis sativus) in India. Plant Dis. 2004, 88: 906-10.1094/PDIS.2004.88.8.906B.View ArticleGoogle Scholar
- Mandal B, Mandal S, Pun KB, Varma A: First report of the association of a nanovirus with foorkey disease of large cardamom in India. Plant Dis. 2004, 88: 428-10.1094/PDIS.2004.88.4.428A.View ArticleGoogle Scholar
- Fauquet CM, Bisaro DM, Briddon RW, Brown JK, Harrison BD, Rybicki EP, Stanley J: Revision of taxonomic criteria for specie demarcation in the family Geminiviridae and an updated list of begomovirus species. Arch Virol. 2003, 148: 405-421. 10.1007/s00705-002-0957-5.View ArticlePubMedGoogle Scholar
- Maruthi MN, Rekha AR, Muniyappa V: Pumpkin yellow vein mosaic disease is caused by two distinct begomoviruses: complete viral sequences and comparative transmission by an indigenous Bemisia tabaci and the introduced B-biotype. EPPO Bull. 2007, 37: 412-419. 10.1111/j.1365-2338.2007.01127.x.View ArticleGoogle Scholar
- Tahir M, Haider MS: First report of Tomato leaf curl New Delhi virus infecting bitter gourd in Pakistan. Plant Pathol. 2005, 54: 807-807. 10.1111/j.1365-3059.2005.01215.x.View ArticleGoogle Scholar
- Guzman P, Sudarshana MR, Seo YS, Rojas MR, Natwick E, Turini T, Mayberry K, Gilbertson RL: A new bipartite geminivirus (begomovirus) causing leaf curl and crumpling in cucurbits in the Imperial Valley of California. Plant Dis. 2000, 84: 488-10.1094/PDIS.2000.84.4.488C.View ArticleGoogle Scholar
- Maruthi MN, Colvin J, Briddon RW, Bull SE, Muniyappa V: Pumpkin yellow vein mosaic virus: a novel begomovirus infecting cucurbits. J Plant Pathol. 2003, 85: 64-65.Google Scholar
- Revill PA, Ha CV, Porchun SC, Vu MT, Dale JL: The complete nucleotide sequence of two distinct geminiviruses infecting cucurbits in Vietnam. Arch Virol. 2003, 148: 1523-1541. 10.1007/s00705-003-0109-6.View ArticlePubMedGoogle Scholar
- Morales FJ, Jones PG: The ecology and epidemiology of whitefly-transmitted viruses in Latin America. Virus Res. 2004, 100: 57-65. 10.1016/j.virusres.2003.12.014.View ArticlePubMedGoogle Scholar
- Chatchawankanphanich O, Chiang BT, Green SK, Singh SJ, Maxwell DP: Nucleotide sequence of a geminivirus associated with tomato leaf curl from India. Plant Dis. 1993, 77: 1168-10.1094/PD-77-1168C.View ArticleGoogle Scholar
- Mansoor S, Khan SH, Saeed M: Evidence for the association of a bipartite geminivirus with tomato leaf curl disease in Pakistan. Plant Dis. 1997, 81: 958-10.1094/PDIS.19126.96.36.1998C.View ArticleGoogle Scholar
- Mansoor S, Khan SH, Hussain M, Zafar Y, Pinner MS, Briddon RW, Stanley J, Markham PG: Association of a begomovirus and nanovirus like molecule with Ageratum yellow vein disease in Pakistan. Plant Dis. 2000, 84: 101-10.1094/PDIS.2000.84.1.101A.View ArticleGoogle Scholar
- Samretwanich K, Chiemsombat P, Kittipakorn K, Ikegami M: Tomato leaf curl geminivirus associated with cucumber yellow leaf disease in Thailand. J Phytopathol. 2000, 148: 615-617.Google Scholar
- Haider MS, Tahir M, Latif S, Briddon RW: First report of Tomato leaf curl New Delhi virus infecting Eclipta prostrata in Pakistan. Plant Pathol. 2005, 55: 285-285. 10.1111/j.1365-3059.2005.01278.x.View ArticleGoogle Scholar
- Zhou X, Liu Y, Calvert L, Munoz C, Otim-Nape GW: Evidence that DNA-A of a geminivirus associated with severe cassava mosaic disease in Uganda has arisen by interspecific recombination. J Gen Virol. 1997, 78: 2101-2111.View ArticlePubMedGoogle Scholar
- Moffat AS: Geminiviruses emerge as serious crop threat. Science. 1999, 286: 1835-10.1126/science.286.5446.1835.View ArticleGoogle Scholar
- Paddidam M, Sawyer S, Fauquet CM: Possible emergence of new geminiviruses by frequent recombination. Virology. 1999, 265: 218-225. 10.1006/viro.1999.0056.View ArticleGoogle Scholar
- Cui X, Tao X, Xie Y, Fauquet CM, Zhou X: A DNA β associated with Tomato yellow leaf curl China virus is required for symptom induction. J Virol. 2004, 78: 13966-13974. 10.1128/JVI.78.24.13966-13974.2004.PubMed CentralView ArticlePubMedGoogle Scholar
- Li ZH, Xie Y, Zhou XP: Tobacco curly shoot virus DNA β is not necessary for infection but intensifies symptoms in a host-dependent manner. Phytopathology. 2005, 95: 902-908. 10.1094/PHYTO-95-0902.View ArticlePubMedGoogle Scholar
- Mansoor S, Qazi J, Amin I, Khatri A, Khan IA, Raza S, Zafar Y, Briddon RW: A PCR-based method, with internal control, for the detection of Banana bunchy top virus in banana. Mol Biotehnol. 2005, 30: 167-170. 10.1385/MB:30:2:167.View ArticleGoogle Scholar
- Duffy S, Holmes EC: Phylogenetic evidence for rapid rates of molecular evolution in the single-stranded DNA begomovirus Tomato yellow leaf curl virus (TYLCV). J Virol. 2008, 82: 957-965. 10.1128/JVI.01929-07.PubMed CentralView ArticlePubMedGoogle Scholar
- Roye ME, Mclaughlin WA, Maxwell DP: The evolution of new virus genes: Interspecies recombination among two geminiviruses from Jamaica. Jamaican J Sci Technol. 2000, 11: 42-46.Google Scholar
- Pita JS, Fondong VN, Sangre A, Otim-Nape GW, Ogwal S, Fauquet CM: Recombination, pseudorecombination and synergism of geminiviruses are determinant keys to the epidemic of severe cassava mosaic disease in Uganda. J Gen Virol. 2001, 82: 655-665.View ArticlePubMedGoogle Scholar
- Harrison BD, Robinson DJ: Another quarter century of great progress in understanding the biological properties of plant viruses. Ann Appl Bio. 2005, 146: 15-37. 10.1111/j.1744-7348.2005.04111.x.View ArticleGoogle Scholar
- Rothenstein D, Haible D, Dasgupta I, Dutt N, Patil BL, Jeske H: Biodiversity and recombination of cassava-infecting begomoviruses from southern India. Arch Virol. 2006, 151: 55-69. 10.1007/s00705-005-0624-8.View ArticlePubMedGoogle Scholar
- Sanderfoot AA, Lazarowitz SG: Getting it together in plant virus movement: Cooperative interactions between bipartite geminivirus movement proteins. Trends Cell Biol. 1996, 6: 353-358. 10.1016/0962-8924(96)10031-3.View ArticlePubMedGoogle Scholar
- Amrao L, Akhter S, Tahir MN, Amin I, Briddon RW, Mansoor S: Cotton leaf curl disease in Sindh province of Pakistan is associated with recombinant begomovirus components. Virus Res. 2010, 153: 161-165. 10.1016/j.virusres.2010.07.003.View ArticlePubMedGoogle Scholar
- Heyraud-Nitschke F, Schumacher S, Laufs J, Schaefer S, Schell J, Gronenborn B: Determination of the origin, cleavage and joining domains of geminivirus Rep proteins. Nucleic Acids Res. 1995, 23: 910-916. 10.1093/nar/23.6.910.PubMed CentralView ArticlePubMedGoogle Scholar
- Laufs J, Schumacher S, Geisler N, Jupin I, Gronenborn B: Identification of the nicking tyrosine of geminivirus Rep protein. FEBS Lett. 1995, 377: 258-262. 10.1016/0014-5793(95)01355-5.View ArticlePubMedGoogle Scholar
- Orozco BM, Bowdoin HL: A DNA structure is required for geminivirus origin function. J Virol. 1996, 270: 148-158.Google Scholar
- Choi IR, Stenger DC: Strain specific determinants of beet curly top geminivirus DNA replication. Virology. 1995, 206: 904-912. 10.1006/viro.1995.1013.View ArticlePubMedGoogle Scholar
- Jupin I, Hericourt F, Benz B, Gronenborn G: DNA replication specificity of TYLCV geminivirus is mediated by the amino-terminal 116 amino acids of the Rep protein. FEBS Lett. 1995, 362: 116-120. 10.1016/0014-5793(95)00221-T.View ArticlePubMedGoogle Scholar
- Gladfelter HJ, Eagle PA, Fontes EPB, Batts LA, Hanley-Bowdoin L: Two domains of the AL1 protein mediate geminivirus origin recognition. Virology. 1997, 239: 186-197. 10.1006/viro.1997.8869.View ArticlePubMedGoogle Scholar
- Chatterji A, Chaterji U, Beachy RN, Fauquet CM: Sequence parameters that determine specificity of binding of the replication-associated protein to its cognate site in two strains of tomato leaf curl virus-New Delhi. Virology. 2000, 273: 341-350. 10.1006/viro.2000.0434.View ArticlePubMedGoogle Scholar
- Chakraborty S, Pandey PK, Banerjee MK, Kallo G, Fauquet CM: Tomato leaf curl Gujarat virus, a new begomovirus species causing a severe leaf curl disease of tomato in Varanasi, India. Virology. 2003, 93: 1485-1495.Google Scholar
- Sanderfoot AA, Ingham DJ, Lazarowitz SG: A viral movement protein as a nuclear shuttle: The geminivirus BR1 movement protein contains domains essential for interaction with BL1 and nuclear localization. Plant Physiol. 1996, 110: 23-33. 10.1104/pp.110.1.23.PubMed CentralView ArticlePubMedGoogle Scholar
- Rojas MR, Hagen C, Lucas WJ, Gilbertson RL: Exploiting chinks in the plant's armor: Evolution and emergence of geminiviruses. Ann Rev Phytopathol. 2005, 43: 361-394. 10.1146/annurev.phyto.43.040204.135939.View ArticleGoogle Scholar
- Berrie LC, Rybicki EP, Rey MEC: Complete nucleotide sequence and host range of South African cassava mosaic virus: further evidence for recombination amongst begomoviruses. J Gen Virol. 2001, 82: 53-58.View ArticlePubMedGoogle Scholar
- Unseld S, Ringel M, Hofer P, Hohnle M, Jeske H, Bedford ID, Markham PG, Frischmuth T: Host range and symptom variation of pseudorecombinant virus produced by two distinct bipartite geminiviruses. Arch Virol. 2000, 145: 1449-1454. 10.1007/s007050070101.View ArticlePubMedGoogle Scholar
- Hofer P, Engel M, Jeske H, Frischmuth T: Nucleotide sequence of a new bipartite geminivirus isolated from the common weed Sida rhombifolia in Costa Rica. J Gen Virol. 1997, 78: 1785-1790.View ArticlePubMedGoogle Scholar
- Briddon RW, Stanley J: Sub-viral agents associated with plant-infecting single-stranded DNA viruses. Virology. 2006, 344: 198-210. 10.1016/j.virol.2005.09.042.View ArticlePubMedGoogle Scholar
- Briddon RW, Patil BL, Bagewadi B, Nawaz-ul-Rehman MS, Fauquet CM: Distinct evolutionary histories of the DNA-A and DNA-B components of bipartite begomoviruses. BMC Evol Biol. 2010, 10: 97-10.1186/1471-2148-10-97.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.