1. KAUTIR (Kerala Agricultural University Theses Information and Retrieval)

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Subject: search.filters.subject.Begomovirus

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    Modeling of cassava-cassava mosaic vrus interactions with computational biology and bioinformatics approach
    (Department of Plant Biotechnology, College of Agriculture,Vellayani, 2019) Rajani, K R; Sreekumar, J
    Every year pathogenic organisms cause billions of dollars’ worth damage to crops and livestock. In agriculture, study of plant-microbe interactions is demanding a special attention to develop management strategies for the destructive pathogen induced diseases that cause huge crop losses every year worldwide. Cassava Mosaic Virus (CMV) is a major viral leaf pathogen that causes disease in cassava. Protein-Protein Interactions (PPIs) play a critical role in initiating pathogenesis and maintaining infection. Understanding the PPI network between a host and pathogen is a critical step for studying the molecular basis of pathogenesis. The experimental study of PPIs at a large scale is very scarce and also the high throughput experimental results show high false positive rate. Hence, there is a need for developing efficient computational models to predict the interaction between host and pathogen in a genome scale, and find novel candidate effectors and/or their targets. In this study, interacting proteins in cassava-CMV interaction is predicted using interolog-based method. The interolog method relies on protein sequence similarity to conduct the PPI prediction. Using this method, 114 PPIs have been predicted between 114 proteins of cassava and 10 proteins of CMV. Functional annotation of the predicted proteins showed the presence of 10 disease resistance protein in cassava that interacts with CMV. The subcellular location of the predicted proteins was found and it showed that major interactions occur in nucleus and chloroplast region. This can be a useful resource to the plant community to characterize the host-pathogen interaction in cassava and CMV. Further, these prediction models can be applied to the agriculturally relevant crops.
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    Nutrient based management of chilli leaf curl virus in Chilli (Capsicum annuum L.)
    (Department of Plant Pathology, College of Agriculture, Vellayani, 2019) Shilpa Sankar; Radhika, N S
    The study entitled “Nutrient based management of Chilli leaf curl virus in Chilli (Capsicum annuum L.) was conducted at Department of Plant Pathology, College of Agriculture, Vellayani from 2017 to 2019. The main objectives were to serologically and molecularly characterize the virus causing leaf curl in chilli and to study the role of nutrient application in the management of the disease. The present investigation was carried out in four experiments viz., collection of Begomovirus infecting chilli from different cultivated areas, symptomatology, serological diagnosis and molecular characterization of the virus causing chilli leaf curl and nutrient based management of chilli leaf curl. The survey was undertaken from December 2018 to March 2019 to investigate the disease incidence in major chilli growing areas of Palakkad (Vadakarapathy and Kozhinjanpara) and Thiruvananthapuram districts (College of Agriculture, Vellayani) of Kerala. In Thiruvananthapuram, the disease incidence ranged from 69.33 to 80 per cent whereas Palakkad recorded maximum incidence of 73.33 per cent in Vadakarapathy village and Kozhinjanpara village recorded the disease incidence of 55.71 to 71.70 per cent. The common symptoms of the disease were upward curling and puckering of leaves, and stunting of whole plant. Other symptoms viz., reduced leaf size, yellowing, petiole elongation, crinkling and mottling of leaves with few or no fruits were also observed. Serological diagnosis of the disease was carried out using triple antibody sandwich – enzyme linked immunosorbent assay (TAS-ELISA) using polyclonal antisera specific to Begomovirus, Sri Lankan cassava mosaic virus (SLCMV). All the samples collected from College of Agriculture, Vellayani were detected with the virus whereas none of the samples from Palakkad district were positive to the virus. Molecular characterization of the virus using universal primers specific to coat protein of Begomovirus viz., AV-AC and DENG through Polymerase chain reaction (PCR) revealed that the DNA isolated from samples of Vellayani could yield an amplicon size of ̴ 550 bp (AV-AC) and ̴ 500 bp (DENG); thus confirming the presence of the virus. But no PCR amplification was observed in any of the samples from Palakkad district. Blast analysis with the sequence of coat protein of Vellayani revealed that the virus had 96.63 per cent similarity with Chilli leaf curl Vellanad virus. Nutrient status of healthy and diseased leaves revealed that the per cent of major nutrients viz., nitrogen (N), phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg); and micronutrients viz., manganese (Mn), zinc (Zn), copper (Cu) and boron (B) in the infected leaves was low compared to the healthy leaves but in sufficient level. Whereas, the per cent of sulphur (S) and iron (Fe) in infected leaves was high and in toxic level. Comparatively higher levels of all the major and micro nutrients were recorded in the soils collected from the infected fields than the soils from the healthy field. A pot culture study was conducted at Department of Plant Pathology in completely randomized design consisting of ten treatments and three replications with chilli variety Vellayani Athulya from May 2019 to August 2019. Cent per cent disease incidence was recorded in all chilli plants before imposing the treatments. Soil samples were taken and analysed for major and micro nutrients at pre-treatment stage. Urea, rajphos, murate of potash, lime and magnesium sulphate (MgSO4) were used as the source of major nutrients like N, P, K, Ca and Mg, respectively. Whereas, manganese sulphate (MnSO4), zinc sulphate (ZnSO4), copper sulphate (CuSO4), borax and potassium silicate were used as source for micronutrients such as Mn, Zn, Cu, B and Si, respectively. After imposing the treatments, the highest coefficient of infection (75.0) was recorded in untreated infected plants whereas, the plants supplemented with nutrients as per package of practices (POP) + B @ 10 kg ha-1, POP + (ZnSO4) @ 20 kg ha-1 and, basal application of 1/2 N + full P + 1/2 K followed by 0.5 per cent foliar application of NPK 19:19:19 at fortnightly recorded the lowest coefficient of infection (25.0). TAS-ELISA conducted with all the experimental plants confirmed the presence of virus. Lower virus titre value was observed in the plants supplemented with nutrients as per POP recorded maximum level of major nutrients. Among the treatments highest fruit yield of 48.85 g plant1 was obtained from plants supplemented with nutrients as per POP + B @ 10 kg ha-1 was found to be most effective in reducing the coefficient of infection with better yield. Thus, the present study revealed that the serological diagnosis of the disease carried out using TAS-ELISA with antisera SLCMV and molecular characterization of the virus using primers AV-AC and DENG through PCR confirmed the presence of virus in Vellayani. The BLAST analysis of Chilli leaf curl Vellayani isolate thus showed 96.63 per cent similarity with Chilli leaf curl Vellanad virus. It was also indicated that Chilli leaf curl virus in chilli could be managed by the application of nutrients as per package of practices recommendation along with boron as borax @ 10 kg ha-1 which need to be validated under field conditions.
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    Development of infectious clones of cassava mosaic virus and their validation
    (Department of Plant Biotechnology, College of Agriculture, Vellayani, 2018) Vishnu Narayanan; Makeshkumar, T
    The study entitled “Development of infectious clones of cassava mosaic virus and their validation” was conducted at the ICAR- Central Tuber Crop Research Institute (ICAR-CTCRI), Sreekariyam, Thiruvananthapuram during 2017- 2018. The major objectives of the study were cloning and characterisation of SLCMV/ICMV infected leaf samples, construction of infectious clones of SLCMV/ICMV and agroinoculation of Nicotiana benthaminana with the partial dimers constructed in order to check the infectiousness of the viral clones. The whole genome amplification of SLCMV/ICMV DNA samples were done and cloned in pUC19 vectors to obtain pSLCMV A7 (2746 bp), pSLCMV B2 (2738 bp) and pICMV A5 (2739 bp) full length clones. The sequence of pSLCMV A7 showed maximum similarity of 99 % with ‘SLCMV-[TVM1]’ sequence in NCBI blast. While the sequence of pSLCMV B2 showed maximum similarity of 99 % with ‘SLCMV-[Ker20]’ sequence in NCBI blast. The sequence of pICMV A5 showed maximum similarity of 95 % with ‘ICMV-[Mah]’ sequence in NCBI blast. In order to develop infectious clones, partial dimers were constructed for SLCMV DNA-A and SLCMV DNA-B and cloned in binary vector pPZP201. These infectious clones were successfully transformed into wild type A. tumefaciens, Ach5 strain by triparental method. Then agroinoculation of N. benthamiana with the constructed partial dimers was found to be successful. After 14 days post inoculation, plants infected with DNA-A + DNA-B partial dimers showed severe symptoms like leaf curling, stunting. The plants infected with partial dimer of DNA-A alone showed mild symptoms like upward leaf curling which confirmed its monopartite lineage. While those plants agroinoculated with partial dimer of DNA-B alone did not show any symptoms. These efficient infectious clones of cassava mosaic virus and their subsequent inoculation technique would provide a major advancement to the resistance development in cassava.
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    Molecular cloning and characterization of virus causing leaf curl disease of capsicum spp.
    (Centre for Plant Biotechnology and Molecular Biology, College of Horticulture, Vellanikkara, 2019) Niranjana Menon, C; Anita Cherian, K
    Chilli is one of the most important crops cultivated across the globe, as vegetable, spice and for industrial purposes. According to the statistics of National Horticulture Board (2017), the crop covers an area of 1860 ha in the state of Kerala with an average production of 12470 tonnes. During the last decade, the threats posed by the emerging begomoviruses infecting solanaceous crops have affected the economic cultivation of chilli. Chilli leaf curl disease caused by Chilli leaf curl virus belonging to the genus Begomovirus and family Geminiviridae is a serious constraint to chilli production in India which causes upto 100 per cent yield loss especially when infected at an early stage of the crop. Considering the importance of the disease, the present study was undertaken with the objective to study the incidence and symptomatology of chilli leaf curl disease and to characterize and clone the coat protein gene of the Chilli leaf curl virus isolates. The project initiated with purposive sampling surveys conducted in eleven different locations of Thrissur district, Kerala to document the incidence and symptomatology of leaf curl disease on chilli plants. The disease incidence recorded during the survey ranged from 43.30 to 85.00 per cent under open field conditions and from 45.75 to 79.40 per cent under protected conditions while the disease severity ranged from 43.60 to 81.54 per cent and from 49.40 to 87.50 per cent, respectively under open field conditions and protected conditions. The symptomatology of chilli leaf curl disease on different parts of the plant such as leaves, internodes, fruits and the whole plant under natural conditions was documented during the survey. The symptoms observed on the leaves of infected chilli plants under natural conditions include upward curling, crinkling, puckering, vein banding, interveinal chlorosis, size reduction of leaf lamina and leaf malformation. The fruits produced by the infected plants showed size reduction and deformation. The infected plants were stunted and bushy in appearance. The transmission of the virus by insect vector, Bemisia tabaci and grafting was studied and the symptoms were documented. The newly emerged leaves after artificial inoculation expressed symptoms such as curling, puckering and crinkling along with stunting of plant growth. Molecular characterization of the four virus isolates collected from various locations of Thrissur district viz., VKA1 VKA2, KAR1 and KOD4 and two isolates viz., VLNY1 and PKD1 collected from Vellayani, Thiruvanathapuram district and from Vithinasseri, Palakkad district, respectively were undertaken. The total genomic DNA from virus infected chilli leaf samples was isolated and subjected to PCR amplification of viral coat protein gene to confirm the presence of virus infection. PCR amplification of the isolated DNA was carried out using two Begomovirus specific degenerate (universal) primers, namely, AV494 / AC1048 (Wyatt and Brown, 1996) and Deng 540 / 541 (Deng et al., 1994). The amplicons of size 550 bp were obtained and were sequenced. The partial coat protein gene of size 550bp were also cloned into the vector pTZ57R/T and transformed into DH5α strain of Escherichia coli and the true recombinants with desirable insert were confirmed by colony PCR. The sequence data obtained in the study were subjected to in silico analysis to assess the diversity of the isolates. The nucleotide BLAST (BLASTn) analysis revealed more than 90 per cent sequence identity with Chilli leaf curl Vellanad virus isolate (Accession No. NC038442.1) from Vellanad region of Thiruvanathapuram district, Kerala. The translated nucleotide - protein BLAST (BLASTx) analysis of the viral sequences revealed more than 96 per cent sequence identity with Chilli leaf curl Vellanad virus coat protein sequence (accession no. YP_009506391.1). The coat protein sequences of all the six isolates were translated into corresponding amino acid sequence by ExPASy Translate tool and were used for further analysis and interpretation. The phylogenetic analysis revealed that, the isolates VKA2, KAR1 and KOD4 had very distinct sequence alignment when compared to other Chilli leaf curl virus isolates from India. The results indicated that, the three isolates viz., VKA2, KAR1 and KOD4 could be new strains of Chilli leaf curl virus infecting chilli. Three, possibly new strains of Chilli leaf curl virus infecting chilli have been identified and hence the study highlights the need for monitoring the emergence of new strains of plant viruses especially begomoviruses infecting solanaceous crops grown in Kerala. As this disease is one of the most important challenges to chilli cultivation, the information generated from the study could also be applied for the timely detection and effective disease management
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    Integrated management of viral diseases of bittergourd (momordica charantia L.)
    (Department of Plant Pathology, College of Agriculture, Vellayani, 2018) Radhika, N S; Umamaheswaran, K
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    Etiology and management of mosaic disease in ginger (Zingiber officinale Roscoe)
    (Department of Plant Pathology, College of Agriculture, Vellayani, 2018) Ananthu, N; Umamaheswaran, K
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    Characterization and management of yellow mosaic disease of black gram (vigna mungo (L.) hepper)
    (Department of Plant Pathology, College of Horticulture, Vellanikkara, 2018) Divya Jayakumar, V J; Sumiya, K V
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    Cloning and expression of coat protein gene of sweet potato leaf curl virus (splcv)
    (Department of Plant Biotechnology, College of Agriculture, Vellayani, 2018) Sruthy, G S; Makeshkumar, T
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    Characterization of Bemisia tabaci (Gennadius) (hemiptera: aleyrodidae), for genetic variability, endosymbionts and vector-virus interactions in cassava
    (Department of Agricultural Entomology, College of Horticulture, Vellanikkara, 2018) Harish, E R; Mani Chellappan
    Cassava is one of the important tuber crops cultivated all over the World. Cassava Mosaic Disease (CMD) is the most important limiting factor in its production. Silverleaf whitefly, Bemisia tabaci (Gennadius) is the vector responsible for the transmission of Cassava mosaic virus in cassava, which causes CMD. Genetic variation among the members of B. tabaci, makes them very difficult to manage. Endosymbionts present in the whitefly system could be a factor responsible for making them a successful sucking pest. There are various kinds of interactions existing between whitefly and the CMV. Studying these interactions precisely will help to understand the behavioural and physiological variations in whiteflies. In this background the present study, “Characterization of Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae), for genetic variability, endosymbionts and vector-virus interactions in cassava” was proposed and carried out at the Department of Agricultural Entomology, College of Horticulture, Vellanikkara, during Mrch 2014 to April 2016, with the objectives to analyse the genetic variability in cassava whitefly, characterization of its endosymbionts and elucidation of cassava whitefly - cassava mosaic virus interactions. Various life stages of B. tabaci were collected from different cassava growing agro ecological zones of Kerala and reared in laboratory as well as in polyhouse at optimum conditions. Genetic variability study was conducted with 10 selected ISSR primers which had shown polymorphism in their banding pattern; with amplicon size ranged between 200bp to 2900bp. Phylogenetic analysis using NTsys software revealed the presence of two major clusters with Sultan Bathery population as out group. Similarity matrix had shown up to 49 per cent variation between the samples. Polymerase chain reaction using mitochondrial cytochrome oxidase1 primers, C1-J2195 and L2-N-3014 had given amplicon of 850bp. Nucleotide sequences had shown variation up to 16.5 per cent and dendrogram generated out of the sequences using MEGA-6 (Neighbor Joining Method) gave two clusters and one out group. Sequence similarity check using reference sequences from NCBI data base indicated the presence of two biotypes, AsiaI and AsiaII5 in cassava plants of Kerala. Morphometric studies were conducted to assess the variations in different pupal and adult characters of thirteen whitefly populations. Significant variations were found in pupal length and pupal width of the biotypes. Pupal length varied between 0.746 mm to 0.668 mm and pupal width varied between 0.539 mm to 0.468 mm in female pupa. Out of 14 characters of pupa studied, variations in length and width were found to be significant. Among seven characters of adults studied, variations in wing, antennal length, body length and width were significant. AsiaI biotype was found to have lesser body length, but more width compared to AsiaII5. AsiaII5 was found to be an important biotype of B. tabaci infesting cassava in 12 out of the 13 locations surveyed. Endosymbiont characterization from whitefly using Next Generation Sequencing (NGS) - Illumina platform revealed the variations in microbiota. At phylum level, Proteobacteria was found at 87.57 per cent in whitefly populations collected from plains. The populations from high ranges contained Firmicutes at 82.67 per cent. Arsenophonus, an ‘indirect helper’ for virus spread by protecting viral coat protein from degradation in insect system with their GroEL chaperones were found at 24. 69 per cent in B. tabaci populations collected from plains. Behavioural and life cycle variation study of B. tabaci using six cassava genotypes had shown that virus infection in B. tabaci altered the dispersal and settling. Speed of movement observed to be maximum at 16.25 cm/s in non- virulent female whiteflies on the genotype CMR-9. Life cycle of virulent and non-virulent whiteflies was found to vary between 19.57 days to 30.77 days. A thorough understanding of genetic variations, endosymbiont diversity and behavioural response to virus could help the researchers in planning proper management strategies for B. tabaci. In future, information generated of such kinds could also help the researchers and policy makers to foresee and manage any possible outbreak of the pest and avoid any havoc caused by them.
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    Identification of potential donors for superior fruit quality traits and genes for resistance to tomato leaf curl virus (ToLCV) In tomato and allied species
    (Department of Plant Breeding and Genetics, College of Agriculture, Vellayani, 2017) Nadkarni Siddhesh Raghvehdra; Jayalekshmy, V G