117 results on '"Gautam, Saurabh"'
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102. Overview of Current Downstream Processing for Modern Viral Vectors
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Cashen, Paul, McLaughlin, Katy, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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103. Filtration Principles and Techniques for Bioprocessing of Viral Vector-Based Therapeutics
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Vergauwen, Laurens, Scanlan, Claire, Krishnan, Ratish, Pandey, Santosh Kumar, Loong, David, Bhushan, Amritanshu, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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104. Recent Advancements and Challenges in Recombinant Expression for Commercial Production of Virus-Like Particles (VLPs)
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Rani, Abhilasha K., Khan, Wajihul Hasan, Banerjee, Manidipa, Rathore, Anurag S., Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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105. Improved Production Strategies for Oncolytic Measles Viruses as a Therapeutic Cancer Treatment
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Eckhardt, Dustin, Bossow, Sascha, Klee, Jan-Philip, Boshof, Björn, Ungerechts, Guy, Czermak, Peter, Salzig, Denise, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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106. Application of NMR Spectroscopy in Viral Assembly Characterization
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Xin, Dongyue, Hawley, Michael, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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107. Phase-Appropriate Potency Assay Development for AAV-Based Gene Therapy Products
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Peters, Elaine E., Pach, Roland, Datta, Shyamtanu, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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108. Quantification of Virus Infectivity: The Key Assay for the Development of Viral Therapeutics
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Businger, Ramona, Hochdorfer, Daniel, Hotter, Dominik, Solzin, Johannes, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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109. Methods and Practical Considerations in Imaging Viral Therapeutics
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Dass, Martin, Xin, Dongyue, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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110. Product-Related Impurities in Therapeutic Virus Bioprocessing
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Ng, Judy King Man, Gautam, Saurabh, editor, Chiramel, Abhilash I., editor, and Pach, Roland, editor
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- 2023
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111. Tri-Trophic Studies Using Cry1Ac- Resistant Diamondback Moth, Plutella Xylostella (L.) Demonstrate No Adverse Effects Of Cry1 Ac On The Entomopathogenic Nematode, Heterorhabditis Bacteriophora Poinar
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Gautam, Saurabh
- Abstract
Plutella xylostella L. (Lepidoptera: Plutellidae), is an important insect pest of brassica crops. This pest is globally distributed and reported to cause annual losses of US $4-5 billion to the world economy. Continuous and intensive use of many classes of insecticides has led to resistance development in some populations of P. xylostella, particularly in the tropics and subtropics where brassica crops are grown year-round and insect pressure is intense. Long distance migration, its ability to establish in new habitats and elimination of local natural enemies from the agroecosystem due to the intense use of broad-spectrum insecticides are some of the reasons that have contributed to outbreaks of this devastating pest. The development and commercialization of insect-resistant genetically modified (IRGM) crops expressing insecticidal crystal (Cry) proteins from the bacterium Bacillus thuringiensis (Bt) have revolutionized insect pest management in two field crops, cotton and corn. In 2012, these crops were grown on more than 69 million hectares worldwide. Several studies have reported that Bt genes coding for insecticidal Cry toxins, when introduced in brassica crops, confer resistance to P. xylostella. Introduction of Bt brassica crops along with other pest management tactics including cultural, chemical and natural enemies could be a feasible solution to keep P. xylostella under control in the near and long term. However, assessing the environmental safety and compatibility of Bt crops with other control measures, particularly with biological control agents, is imperative. Entomopathogenic nematodes (EPN) in the family Steinernematidae and Heterorhabditidae are important biological control agents for many insect pests. Laboratory and field studies have reported the potential use of EPN for the control of P. xylostella. In the future, if Bt brassica crops are commercialized, EPN applied against P. xylostella may become exposed to Bt proteins directly through root exudates or indirectly by feeding on P. xylostella that developed on Bt crops. The main purpose of this research project was to assess the potential effects of Cry1Ac on Heterorhabditis bacteriophora Poinar (Rhabditida: Heterorhabditidae) under tri-trophic conditions. Using Cry1Ac-resistant P. xylostella larvae as hosts, we evaluated the potential impact of Cry1Ac-expressing broccoli on several fitness parameters of H. bacteriophora. Virulence, reproductive potential, time of emergence and preference of H. bacteriophora for the host (P. xylostella) were not significantly affected when Cry1Ac-resistant P. xylostella larvae were reared on leaves of Cry1Ac or non-Bt broccoli. Also the above-mentioned parameters of the subsequent generation of H. bacteriophora did not differ between nematodes obtained from P. xylostella reared on Cry1Ac broccoli compared to those obtained from P. xylostella reared on non-Bt broccoli.
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- 2014
112. The Hsc70 disaggregation machinery removes monomer units directly from α-synuclein fibril ends
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Tuomas P. J. Knowles, Christopher M. Dobson, Quentin Peter, Ewa Andrzejewska, Michele Vendruscolo, Matthias Schneider, Georg Krainer, F. Ulrich Hartl, Therese W. Herling, Francesco Simone Ruggeri, Andreas Bracher, Alyssa M. Miller, Victoria A. Trinkaus, Saurabh Gautam, Schneider, Matthias M [0000-0002-1894-1859], Gautam, Saurabh [0000-0003-0366-6169], Krainer, Georg [0000-0002-9626-7636], Peter, Quentin AE [0000-0002-8018-3059], Ruggeri, Francesco Simone [0000-0002-1232-1907], Vendruscolo, Michele [0000-0002-3616-1610], Bracher, Andreas [0000-0001-8530-7594], Hartl, F Ulrich [0000-0002-7941-135X], Knowles, Tuomas PJ [0000-0002-7879-0140], Apollo - University of Cambridge Repository, Schneider, Matthias M. [0000-0002-1894-1859], Peter, Quentin A. E. [0000-0002-8018-3059], Hartl, F. Ulrich [0000-0002-7941-135X], Knowles, Tuomas P. J. [0000-0002-7879-0140], Peter, Quentin A E [0000-0002-8018-3059], and Knowles, Tuomas P J [0000-0002-7879-0140]
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Amyloid ,631/45/470/2284 ,147/3 ,123 ,Science ,Kinetics ,General Physics and Astronomy ,macromolecular substances ,Fibril ,General Biochemistry, Genetics and Molecular Biology ,101/62 ,639/638/440/56 ,chemistry.chemical_compound ,Single-molecule biophysics ,Biophysical chemistry ,Chaperones ,Escherichia coli ,Life Science ,Humans ,HSP70 Heat-Shock Proteins ,Fragmentation (cell biology) ,82/62 ,Synucleinopathies ,Multidisciplinary ,'de novo' protein folding ,HSC70 Heat-Shock Proteins ,article ,Parkinson Disease ,General Chemistry ,HSP40 Heat-Shock Proteins ,humanities ,Monomer ,631/57/2272/1590 ,chemistry ,alpha-Synuclein ,Biophysics ,631/57/2265 ,α synuclein ,631/45/470/1981 ,Protein aggregation ,Molecular Chaperones - Abstract
Funder: EC | EC Seventh Framework Programm | FP7 Ideas: European Research Council (FP7-IDEAS-ERC - Specific Programme: "Ideas" Implementing the Seventh Framework Programme of the European Community for Research, Technological Development and Demonstration Activities (2007 to 2013)); doi: https://doi.org/10.13039/100011199, Funder: EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council); doi: https://doi.org/10.13039/100010663, Molecular chaperones contribute to the maintenance of cellular protein homoeostasis through assisting de novo protein folding and preventing amyloid formation. Chaperones of the Hsp70 family can further disaggregate otherwise irreversible aggregate species such as α-synuclein fibrils, which accumulate in Parkinson’s disease. However, the mechanisms and kinetics of this key functionality are only partially understood. Here, we combine microfluidic measurements with chemical kinetics to study α-synuclein disaggregation. We show that Hsc70 together with its co-chaperones DnaJB1 and Apg2 can completely reverse α-synuclein aggregation back to its soluble monomeric state. This reaction proceeds through first-order kinetics where monomer units are removed directly from the fibril ends with little contribution from intermediate fibril fragmentation steps. These findings extend our mechanistic understanding of the role of chaperones in the suppression of amyloid proliferation and in aggregate clearance, and inform on possibilities and limitations of this strategy in the development of therapeutics against synucleinopathies.
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- 2021
113. Palynology and detrital zircon geochronology of the Carboniferous Fenestella Shale Formation of the Tethyan realm in Kashmir Himalaya: Implications for global correlation and floristic evolution.
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Agnihotri, Deepa, Pandita, Sundeep K., Tewari, Rajni, Ram-Awatar, null, Linnemann, Ulf, Pillai, S. Suresh K., Joshi, Arun, Gautam, Saurabh, and Kumar, Kamlesh
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PALYNOLOGY , *ZIRCON , *CARBONIFEROUS Period , *SHALE , *SEDIMENTARY rocks - Abstract
First palynological data, supplemented by detrital zircon U–Pb ages, from the Fenestella Shale Formation near the Gund Village in the Banihal area of Jammu and Kashmir State, India, provide new insights into the floristic evolution of Gondwana during the Late Palaeozoic, especially in India, from where the Carboniferous–Permian macro- and microfloral records are impoverished. We also present a first approach to the palynological correlation of the Carboniferous–Permian palynoassemblages described from the various Gondwana countries. The palynomorphs from the Fenestella Shale Formation are fairly well preserved and diversified and include 11 genera and 18 species. While the trilete spores and striate bisaccate pollen grains are scarce, monosaccate pollen taxa mainly – Parasaccites, Plicatipollenites and Potonieisporites are dominant . The assemblage is most similar to the Parasaccites korbaensis palynozone of the Lower Gondwana basins of the Indian peninsula and the Stage 2 palynozone of the late Carboniferous of east Australia. Besides, it is comparable with the known Carboniferous assemblages of Pakistan, Yemen and South America; Carboniferous-early Permian assemblages of South Africa and Permian assemblages of Antarctica. The sediment source of the siliciclastic shelf and delta deposits intercalated in the Fenestella Shale Formation is a hinterland in which Precambrian rocks dominantly were exposed and the Th–U ratios of detrital zircons suggest, that most rocks exposed on the erosion level in the hinterland had a felsic composition. The youngest U–Pb zircon age of the investigated fossiliferous strata is 329 ± 16 Ma (late Visean to early Serpukhovian), providing a maximum age of deposition of the studied succession. Based on the affinities of the palynofloral assemblage and earlier palaeontological records, a warm, temperate and arid climate has been inferred for the Fenestella Shale Formation. [ABSTRACT FROM AUTHOR]
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- 2018
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114. A Novel α-L-Arabinofuranosidase of Family 43 Glycoside Hydrolase (Ct43Araf) from Clostridium thermocellum.
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Ahmed, Shadab, Luis, Ana Sofia, Bras, Joana L. A., Ghosh, Arabinda, Gautam, Saurabh, Gupta, Munishwar N., Fontes, Carlos M. G. A., and Goyal, Arun
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ARABINOFURANOSIDASES , *GLYCOSIDASES , *CLOSTRIDIUM thermocellum , *COMPARATIVE studies , *BIOCHEMISTRY , *RECOMBINANT proteins , *CARBOHYDRATES - Abstract
The study describes a comparative analysis of biochemical, structural and functional properties of two recombinant derivatives from Clostridium thermocellum ATCC 27405 belonging to family 43 glycoside hydrolase. The family 43 glycoside hydrolase encoding α-L-arabinofuranosidase (Ct43Araf) displayed an N-terminal catalytic module CtGH43 (903 bp) followed by two carbohydrate binding modules CtCBM6A (405 bp) and CtCBM6B (402 bp) towards the C-terminal. Ct43Araf and its truncated derivative CtGH43 were cloned in pET-vectors, expressed in Escherichia coli and functionally characterized. The recombinant proteins displayed molecular sizes of 63 kDa (Ct43Araf) and 34 kDa (CtGH43) on SDS-PAGE analysis. Ct43Araf and CtGH43 showed optimal enzyme activities at pH 5.7 and 5.4 and the optimal temperature for both was 50°C. Ct43Araf and CtGH43 showed maximum activity with rye arabinoxylan 4.7 Umg−1 and 5.0 Umg−1, respectively, which increased by more than 2-fold in presence of Ca2+ and Mg2+ salts. This indicated that the presence of CBMs (CtCBM6A and CtCBM6B) did not have any effect on the enzyme activity. The thin layer chromatography and high pressure anion exchange chromatography analysis of Ct43Araf hydrolysed arabinoxylans (rye and wheat) and oat spelt xylan confirmed the release of L-arabinose. This is the first report of α-L-arabinofuranosidase from C. thermocellum having the capacity to degrade both p-nitrophenol-α-L-arabinofuranoside and p-nitrophenol-α-L-arabinopyranoside. The protein melting curves of Ct43Araf and CtGH43 demonstrated that CtGH43 and CBMs melt independently. The presence of Ca2+ ions imparted thermal stability to both the enzymes. The circular dichroism analysis of CtGH43 showed 48% β-sheets, 49% random coils but only 3% α-helices. [ABSTRACT FROM AUTHOR]
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- 2013
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115. First report of Sw-5 resistance-breaking strain of tomato spotted wilt orthotospovirus infecting tomato in Texas.
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Chinnaiah S, Gautam S, Workneh F, Crosby K, Rush C, and Gadhave KR
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Tomato spotted wilt orthotospovirus (TSWV) is one of the most devastating plant viruses causing crop disease epidemics of global economic significance. A single dominant resistant gene 'Sw-5' offering a broad-spectrum resistance to multiple orthotospoviruses was introduced in tomato cultivars. However, multiple resistance-breaking strains of TSWV were reported worldwide (Ciuffo 2005; Zaccardelli et al. 2008; Batuman et al. 2017; di Rienzo et al. 2018). Symptoms suggestive of orthotospoviral infection including stunting, bronzing, and inward rolling of leaves, and concentric necrotic spots on leaves, petioles, and fruits were observed in two TSWV-resistant tomato cultivars ('BL163' and 'HT 2') planted in a tomato variety trial in Bushland, TX in 2022. Leaf tissues from 45 resistant tomato plants (symptomatic or asymptomatic) from both resistant cultivars were tested using a TaqMan probe-based qPCR assay targeting a 200bp region in nucleoprotein (N) of the TSWV (Gautam et al. 2022). While 25 of those samples tested positive for TSWV, only ten expressed characteristic disease symptoms described above. The possibility of mixed infection in those samples with other endemic viruses in the region viz., alfalfa mosaic virus, groundnut ringspot orthotospovirus, tobacco mosaic virus, tomato chlorotic spot orthotospovirus, tomato mosaic virus, tomato necrotic streak virus, tomato ringspot virus, and tomato torrado virus was discounted through RT-PCR analysis (Kumar et al. 2011; Verbeek et al. 2012; Bratsch et al. 2018). To test the RB phenotype of the observed putative TSWV-RB strains, three-week-old tomato plants from eight commercially available TSWV resistant cultivars and one non-resistant cultivar (n=10 each) were mechanically inoculated with leaf tissues collected from a single symptomatic plant from one of the field-grown resistant cultivars. The experiment was replicated twice. Hypersensitive response was observed on all inoculated leaves of resistant plants one week post inoculation. Furthermore, all eight resistant cultivars started expressing local and systemic TSW symptoms 12 to 16 days post inoculation (dpi), while non-resistant cultivar started expressing symptoms at 9 dpi. TSW incidence across all resistant cultivars was 30-70%, while in susceptible cultivar it was 90%. Symptoms exhibited by all resistant cultivars resembled those of symptoms observed in field collected plants. The expression of Sw-5 gene in all eight resistant cultivars and the lack thereof in a susceptible cultivar was confirmed using Sw-5b specific primers and using Actin as a housekeeping gene in qRT-PCR (Islam et al. 2022). The RB strains in Sw-5 resistant tomato in California (Batuman et al. 2017) had the C118Y mutation in the TSWV NSm protein, consistent with the original reporting of C118Y or T120N RB mutations in 11 TSWV isolates from Spain (NCBI accession # HM015517 & HM015518) (Lopez et al. 2011). The nucleotide and amino acid sequence analysis of NSm gene from Bushland RB isolates from four resistant cultivars (NCBI accessions # OP810513-14 [field], OQ247901-05 [mechanically inoculated]) shared 98.9 and 99.4% homology with the Californian NSm sequences of TSWV RB tomato isolate (KX898453 and ASO67371), respectively. While the Nsm C118Y or T120N RB mutations were absent in all Bushland TSWV RB isolates, they had six additional unique point mutations across the NSm (I163V, P227Q, V290I, N293S, V294I, K296Q), which could potentially be responsible for resistance breaking. Despite the lack of C118Y or T120N RB mutations, Bushland isolates were capable of disrupting Sw-5-mediated TSWV resistance in all eight commercial resistant tomato cultivars. This study suggests a new or a different class of fundamental mechanisms are likely to be responsible for resistance breaking in Sw-5b resistant tomatoes. The new RB strain/s of TSWV therefore pose a substantial threat to tomato production in TX and other tomato-growing regions of the US.
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- 2023
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116. The Hsc70 disaggregation machinery removes monomer units directly from α-synuclein fibril ends.
- Author
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Schneider MM, Gautam S, Herling TW, Andrzejewska E, Krainer G, Miller AM, Trinkaus VA, Peter QAE, Ruggeri FS, Vendruscolo M, Bracher A, Dobson CM, Hartl FU, and Knowles TPJ
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- Amyloid metabolism, Escherichia coli, HSC70 Heat-Shock Proteins genetics, HSP40 Heat-Shock Proteins, HSP70 Heat-Shock Proteins metabolism, Humans, Kinetics, Parkinson Disease metabolism, HSC70 Heat-Shock Proteins metabolism, Molecular Chaperones metabolism, alpha-Synuclein metabolism
- Abstract
Molecular chaperones contribute to the maintenance of cellular protein homoeostasis through assisting de novo protein folding and preventing amyloid formation. Chaperones of the Hsp70 family can further disaggregate otherwise irreversible aggregate species such as α-synuclein fibrils, which accumulate in Parkinson's disease. However, the mechanisms and kinetics of this key functionality are only partially understood. Here, we combine microfluidic measurements with chemical kinetics to study α-synuclein disaggregation. We show that Hsc70 together with its co-chaperones DnaJB1 and Apg2 can completely reverse α-synuclein aggregation back to its soluble monomeric state. This reaction proceeds through first-order kinetics where monomer units are removed directly from the fibril ends with little contribution from intermediate fibril fragmentation steps. These findings extend our mechanistic understanding of the role of chaperones in the suppression of amyloid proliferation and in aggregate clearance, and inform on possibilities and limitations of this strategy in the development of therapeutics against synucleinopathies., (© 2021. The Author(s).)
- Published
- 2021
- Full Text
- View/download PDF
117. Virus-virus interactions in a plant host and in a hemipteran vector: Implications for vector fitness and virus epidemics.
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Gautam S, Gadhave KR, Buck JW, Dutta B, Coolong T, Adkins S, and Srinivasan R
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- Animals, Begomovirus genetics, Begomovirus metabolism, Coinfection virology, Crinivirus genetics, Crinivirus metabolism, Female, Hemiptera virology, Male, Plant Viruses classification, Genetic Fitness, Insect Vectors genetics, Insect Vectors virology, Microbial Interactions, Plant Viruses metabolism
- Abstract
Mixed virus infection in host plants can differentially alter the plant phenotype, influence vector fitness, and affect virus acquisition and inoculation by vectors than single-virus infection. Vector acquisition of multiple viruses from multiple host plants could also differentially affect vector fitness and virus inoculation than acquisition of one virus. Whitefly-virus pathosystems in the southern United States include both the above-stated facets. For the first facet, this study examined the effects of single and mixed infection of cucurbit leaf crumple virus (CuLCrV, a begomovirus) and cucurbit yellow stunting disorder virus (CYSDV, a crinivirus) infecting squash on whitefly (Bemisia tabaci Gennadius MEAM1) host preference and fitness. Mixed infection of CuLCrV and CYSDV in squash plants severely altered their phenotype than single infection. The CYSDV load was reduced in mixed-infected squash plants than in singly-infected plants. Consequently, whiteflies acquired reduced amounts of CYSDV from mixed-infected plants than singly-infected plants. No differences in CuLCrV load were found between singly- and mixed-infected squash plants, and acquisition of CuLCrV by whiteflies did not vary between singly- and mixed-infected squash plants. Both singly- and mixed-infected plants similarly affected whitefly preference, wherein non-viruliferous and viruliferous (CuLCrV and/or CYSDV) whiteflies preferred non-infected plants over infected plants. The fitness study involving viruliferous and non-viruliferous whiteflies revealed no differences in developmental time and fecundity. For the second facet, this study evaluated the effects of individual or combined acquisition of tomato-infecting tomato yellow leaf curl virus (TYLCV, a begomovirus) and squash-infecting CuLCrV on whitefly host preference and fitness. Whiteflies that acquired both CuLCrV and TYLCV had significantly lower CuLCrV load than whiteflies that acquired CuLCrV alone, whereas TYLCV load remained unaltered when acquired individually or in conjunction with CuLCrV. Whitefly preference was not affected following individual or combined virus acquisition. Viruliferous (CuLCrV and/or TYLCV) whiteflies preferred to settle on non-infected tomato and squash plants. The mere presence of CuLCrV and/or TYLCV in whiteflies did not affect their fitness. Taken together, these results indicate that mixed infection of viruses in host plants and acquisition of multiple viruses by the vector could have implications for virus accumulation, virus acquisition, vector preference, and epidemics that sometimes are different from single-virus infection or acquisition., (Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
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