{"id":86,"date":"2022-10-14T20:09:31","date_gmt":"2022-10-14T20:09:31","guid":{"rendered":"https:\/\/research.agrilife.org\/gadhavelab\/?page_id=86"},"modified":"2026-03-06T17:02:14","modified_gmt":"2026-03-06T17:02:14","slug":"publications","status":"publish","type":"page","link":"https:\/\/research.agrilife.org\/gadhavelab\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<div class=\"wp-block-cover alignfull is-light wp-duotone-unset-1\" style=\"min-height:500px;aspect-ratio:unset;\"><img loading=\"lazy\" decoding=\"async\" width=\"2560\" height=\"1706\" class=\"wp-block-cover__image-background wp-image-134\" alt=\"Small insects on a leaf\" src=\"http:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-scaled.jpeg\" style=\"object-position:50% 46%\" data-object-fit=\"cover\" data-object-position=\"50% 46%\" srcset=\"https:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-scaled.jpeg 2560w, https:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-300x200.jpeg 300w, https:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-1024x683.jpeg 1024w, https:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-768x512.jpeg 768w, https:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-1536x1024.jpeg 1536w, https:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-2048x1365.jpeg 2048w, https:\/\/research.agrilife.org\/gadhavelab\/wp-content\/uploads\/sites\/23\/2022\/10\/AdobeStock_479511243-4-600x400.jpeg 600w\" sizes=\"auto, (max-width: 2560px) 100vw, 2560px\" \/><span aria-hidden=\"true\" class=\"wp-block-cover__background has-background-dim-30 has-background-dim\" style=\"background-color:#FFF\"><\/span><div class=\"wp-block-cover__inner-container is-layout-flow wp-block-cover-is-layout-flow\">\n<div style=\"padding-left:8%;padding-right:8%\" class=\"wp-block-genesis-blocks-gb-container narrow-content fade-up light-text gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\" style=\"max-width:1200px\">\n<h1 class=\"wp-block-heading bold-text fade-in-up\" id=\"gadhaveresearch\">Publications<\/h1>\n\n\n\n<p class=\"fade-in-up\">Publications of The Gadhave Lab<\/p>\n<\/div><\/div><\/div>\n<\/div><\/div>\n\n\n\n<div style=\"padding-left:8%;padding-right:8%;padding-bottom:10%;padding-top:10%\" class=\"wp-block-genesis-blocks-gb-container gb-block-container alignfull\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\" style=\"max-width:1200px\">\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h2 class=\"wp-block-heading\"><strong>Preprints (Under Review)<\/strong><\/h2>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">1. Field evidence for asymmetric regulation of wheat streak mosaic virus and Triticum mosaic virus across the wheat\u2013wheat curl mite interface<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam, S and Gadhave, KR*. Field evidence for asymmetric regulation of wheat streak mosaic virus and Triticum mosaic virus across the wheat\u2013wheat curl mite interface. Preprint available at Preprints.org: <a href=\"https:\/\/nam10.safelinks.protection.outlook.com\/?url=https%3A%2F%2Fwww.preprints.org%2Fmanuscript%2F202602.1541%2Fv1&amp;data=05%7C02%7Ckiran.gadhave%40ag.tamu.edu%7C171483fb4468458090a308de744e09c3%7C9fd7580a64724d9ca142d131d3a7a116%7C0%7C0%7C639076075699050203%7CUnknown%7CTWFpbGZsb3d8eyJFbXB0eU1hcGkiOnRydWUsIlYiOiIwLjAuMDAwMCIsIlAiOiJXaW4zMiIsIkFOIjoiTWFpbCIsIldUIjoyfQ%3D%3D%7C0%7C%7C%7C&amp;sdata=FX29Fz7rUelpQezVJSfOSBwMiJKYjkRbz%2F9fxbXL1II%3D&amp;reserved=0\" target=\"_blank\" rel=\"noreferrer noopener\">https:\/\/www.preprints.org\/manuscript\/202602.1541\/v1<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>Peer-reviewed<\/strong><\/h2>\n\n\n\n<h3 class=\"wp-block-heading\">2026<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">34. Machine learning reveals microclimate-specific drivers of a cosmopolitan supervector\u2019s population dynamics<\/summary><div class=\"gb-accordion-text\">\n<p>Arora, AK, Anderson, N and Gadhave, KR*. Machine learning reveals microclimate-specific drivers of a cosmopolitan supervector\u2019s population dynamics. <em>Ecological Informatics<\/em>. <a href=\"https:\/\/doi.org\/10.1016\/j.ecoinf.2026.103690\">https:\/\/doi.org\/10.1016\/j.ecoinf.2026.103690<\/a>  <\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">33. Hijacked highways: Plant virus modulation of vector proteins from entry to exit<\/summary><div class=\"gb-accordion-text\">\n<p>Arora, AK, Puri, U and Gadhave, KR*. (2026). Hijacked highways: Plant virus modulation of vector proteins from entry to exit. <em>Current Opinion in Virology<\/em> <a href=\"https:\/\/doi.org\/10.3390\/v17071010\"><\/a>(Accepted).<\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">32. Resistance breaking: Integrated genomic and phenotypic insights into&nbsp;<em>Orthotospovirus tomatomaculae<\/em>&nbsp;strains overcoming&nbsp;<em>Sw-5b<\/em>&nbsp;and&nbsp;<em>Tsw<\/em>&nbsp;resistance<\/summary><div class=\"gb-accordion-text\">\n<p>Chinnaiah, S, Netla, VR, Arora, AK, Srinivasan, R and Gadhave, KR*. (2026.) Resistance breaking: Integrated genomic and phenotypic insights into&nbsp;<em>Orthotospovirus tomatomaculae<\/em>&nbsp;strains overcoming&nbsp;<em>Sw-5b<\/em>&nbsp;and&nbsp;<em>Tsw<\/em>&nbsp;resistance. <em>BMC Genomic<\/em>s. <br><a href=\"https:\/\/doi.org\/10.1186\/s12864-026-12682-2\">https:\/\/doi.org\/10.1186\/s12864-026-12682-2<\/a>    &nbsp;<\/p>\n<\/div><\/details><\/div>\n\n\n\n<h3 class=\"wp-block-heading\">2025<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">31. Impact of wheat resistance genes on wheat curl mite fitness and wheat streak mosaic dynamics under single and mixed infections<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam, S and Gadhave, KR*. (2025). Impact of wheat resistance genes on wheat curl mite fitness and wheat streak mosaic dynamics under single and mixed infections. <em>Viruses<\/em>. <a href=\"https:\/\/doi.org\/10.3390\/v17071010\">https:\/\/doi.org\/10.3390\/v17071010<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">30. Novel strains of tomato spotted wilt orthotospovirus (TSWV) are transmitted by western flower thrips in a context-specific manner<\/summary><div class=\"gb-accordion-text\">\n<p>Chinnaiah, S, Arora, A and Gadhave, KR*. (2025). Novel strains of tomato spotted wilt orthotospovirus (TSWV) are transmitted by western flower thrips in a context-specific manner. PLOS One. <a href=\"https:\/\/doi.org\/10.1371\/journal.pone.0323037\">https:\/\/doi.org\/10.1371\/journal.pone.0323037<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<h3 class=\"wp-block-heading\">2024<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">29. <em>Tsw<\/em>-resistant pepper cultivars offer limited protection against resistance-breaking isolates of tomato spotted wilt virus<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam, S, Workneh, F, Chinnaiah, S, Rush, CM, Xue, Q, Anderson, N, Crosby, KM and Gadhave, KR*. (2024). <em>Tsw<\/em>-resistant pepper cultivars offer limited protection against resistance-breaking isolates of tomato spotted wilt virus. <em>Plant Health Progress<\/em>. <a href=\"https:\/\/doi.org\/10.1094\/PHP-08-24-0075-RS\">https:\/\/doi.org\/10.1094\/PHP-08-24-0075-RS<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">28. Quantifying seasonal thrips population dynamics in relation to temperature and wheat senescence<\/summary><div class=\"gb-accordion-text\">\n<p>Workneh, F, Ehrlich, B, Herron, B, Chinnaiah, S, Gautam, S, Gadhave, KR* and Rush, CM. (2024). Quantifying seasonal thrips population dynamics in relation to temperature and wheat senescence. <em>Entomologia Experimentalis et Applicata<\/em> 172: 446\u2013453. <a href=\"https:\/\/doi.org\/10.1111\/eea.13428 \">https:\/\/doi.org\/10.1111\/eea.13428 <\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">27. Using Raman spectroscopy for early detection of resistance-breaking strains of tomato spotted wilt orthotospovirus in tomatoes<\/summary><div class=\"gb-accordion-text\">\n<p>Ju\u00e1rez ID, Steczkowski MX, Chinnaiah S, Rodriguez A, Gadhave KR* &amp; Kurouski D* (2024). Using Raman spectroscopy for early detection of resistance-breaking strains of tomato spotted wilt orthotospovirus in tomatoes.&nbsp;<em>Frontiers in Plant Sci<\/em>ence&nbsp;14:1283399. <a href=\"https:\/\/doi.org\/10.3389\/fpls.2023.1283399\">https:\/\/doi.org\/10.3389\/fpls.2023.1283399<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<h3 class=\"wp-block-heading\">2023<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">26. Novel strains of a pandemic plant virus, tomato spotted wilt orthotospovirus (TSWV), increase vector fitness and modulate virus transmission in a resistant host<\/summary><div class=\"gb-accordion-text\">\n<p>Chinnaiah, S, Gautam, S, Herron, B, Workneh, F, Rush, C &amp;&nbsp;Gadhave, KR*&nbsp;(2023). Novel strains of a pandemic plant virus, tomato spotted wilt orthotospovirus (TSWV), increase vector fitness and modulate virus transmission in a resistant host.&nbsp;<em>Frontiers in Microbiology<\/em>. <a href=\"https:\/\/doi.org\/10.3389\/fmicb.2023.1257724\">doi: 10.3389\/fmicb.2023.1257724<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">25. Effects of host plants and their infection status on acquisition and inoculation of a plant virus by its Hemipteran vector<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam S, Gadhave KR, Buck JW, Dutta B, Coolong T, Adkins S, Simmons AM, Srinivasan R. (2023). Effects of host plants and their infection status on acquisition and inoculation of a plant virus by its Hemipteran vector.&nbsp;<em>Pathogens<\/em>. <a href=\"https:\/\/doi.org\/10.3390\/pathogens12091119\">https:\/\/doi.org\/10.3390\/pathogens12091119 <\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">24. Seed transmission of wheat streak mosaic virus and Triticum mosaic virus in differentially resistant wheat cultivars<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam, S, Chinnaiah, S, Herron, B, Workneh, F, Rush, C &amp;&nbsp;Gadhave, KR*&nbsp;(2023). Seed transmission of wheat streak mosaic virus and Triticum mosaic virus in differentially resistant wheat cultivars.&nbsp;<em>Viruses<\/em>. <a href=\"https:\/\/doi.org\/10.3390\/v15081774\">https:\/\/doi.org\/10.3390\/v15081774<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">23. First report of <em>Sw-5<\/em> resistance-breaking strain of tomato spotted wilt orthotospovirus infecting tomato in Texas<\/summary><div class=\"gb-accordion-text\">\n<p>Chinnaiah, S, Gautam, S, Workneh, F, Crosby, K, Rush, C &amp; Gadhave, KR. (2023). First report of <em>Sw-5<\/em> resistance-breaking strain of tomato spotted wilt orthotospovirus infecting tomato in Texas. <em>Plant Diseas<\/em>e. <a href=\"https:\/\/doi.org\/10.1094\/PDIS-11-22-2699-PDN\">https:\/\/doi.org\/10.1094\/PDIS-11-22-2699-PDN<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">22. First report of a resistance-breaking strain of tomato spotted wilt orthotospovirus infecting <em>Capsicum annuum<\/em> with the <em>Tsw<\/em> resistance gene in Texas<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam, S, Chinnaiah, S, Workneh, F, Crosby, K, Rush, C &amp; Gadhave, KR. (2023). First report of a resistance-breaking strain of tomato spotted wilt orthotospovirus infecting <em>Capsicum annuum<\/em> with the <em>Tsw<\/em> resistance gene in Texas. <em>Plant Diseas<\/em>e. <a href=\"https:\/\/doi.org\/10.1094\/PDIS-09-22-2274-PDN\">https:\/\/doi.org\/10.1094\/PDIS-09-22-2274-PDN<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<h3 class=\"wp-block-heading\">2022<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">21. Confirmatory detection and identification of biotic and abiotic stresses in wheat using Raman spectroscopy<\/summary><div class=\"gb-accordion-text\">\n<p>Higgins, S, Sereda, V, Herron, B, Gadhave, KR &amp; Kurouski, D. (2022). Confirmatory detection and identification of biotic and abiotic stresses in wheat using Raman spectroscopy. <em>Frontiers in Plant Science<\/em>. <a href=\"https:\/\/doi.org\/10.3389\/fpls.2022.1035522\">https:\/\/doi.org\/10.3389\/fpls.2022.1035522<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">20. A comparative analysis of RNA isolation methods optimized for high-throughput detection of viral pathogens in California\u2019s regulatory and disease management program for citrus propagative materials<\/summary><div class=\"gb-accordion-text\">\n<p>Dang, T, Bodaghi, S, Osman, F, Wang, J, Rucker, T, Tan, S-H, Huang, A, Pagliaccia, D, Comstock, S, Lavagi-Craddock, I, Gadhave, KR \u2026 &amp; Vidalakis, G. (2022). A comparative analysis of RNA isolation methods optimized for high-throughput detection of viral pathogens in California\u2019s regulatory and disease management program for citrus propagative materials. <em>Frontiers in Agronomy<\/em>. <a href=\"https:\/\/doi.org\/10.3389\/fagro.2022.911627\">https:\/\/doi.org\/10.3389\/fagro.2022.911627<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">19. Soil-dwelling <em>Bacillus<\/em> spp. affect aphid infestation of calabrese and natural enemy responses in a context-specific manner<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR* &amp; Gange, A. (2022). Soil-dwelling <em>Bacillus<\/em> spp. affect aphid infestation of calabrese and natural enemy responses in a context-specific manner. <em>Agricultural and Forest Entomology<\/em>. <a href=\"https:\/\/doi.org\/10.1111\/afe.12507\">https:\/\/doi.org\/10.1111\/afe.12507<\/a><\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2021<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">18. Complete nucleotide sequence, genome organization and comparative genomic analyses of citrus yellow vein associated virus (CYVaV)<\/summary><div class=\"gb-accordion-text\">\n<p>Kwon, S-J, Bodaghi, S, Dang, Gadhave, KR*, Ho, T, Osman, F, Maher, AR, Tzanetakis, IE, Simon, AE &amp; Vidalakis, G*. (2021). Complete nucleotide sequence, genome organization and comparative genomic analyses of citrus yellow vein associated virus (CYVaV). <em>Frontiers in Microbiology<\/em>. <a href=\"https:\/\/doi.org\/10.3389\/fmicb.2021.683130\">https:\/\/doi.org\/10.3389\/fmicb.2021.683130<\/a><\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2020<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">17. Aphid transmission of <em>Potyvirus<\/em>: the largest plant-infecting RNA virus genus<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR<sup>\u2020<\/sup>*, Gautam, S<sup>\u2020<\/sup>, Rasmussen, D &amp; Srinivasan, R. (2020). Aphid transmission of <em>Potyvirus<\/em>: the largest plant-infecting RNA virus genus. <em>Viruses<\/em>. <a href=\"https:\/\/doi.org\/10.3390\/v12070773\">https:\/\/doi.org\/10.3390\/v12070773<\/a> <sup>\u2020<\/sup>Equal contribution.<\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">16. Low frequency of cucurbit leaf crumple virus horizontal and vertical transmission in whitefly<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR*, Gautam, S, Dutta, B, Coolong, T, Adkins, S &amp; Srinivasan, R. (2020). Low frequency of cucurbit leaf crumple virus horizontal and vertical transmission in whitefly <em>Bemisia tabaci<\/em> Gennadius. <em>Phytopathology.<\/em> <a href=\"https:\/\/doi.org\/10.1094\/PHYTO-09-19-0337-R\">https:\/\/doi.org\/10.1094\/PHYTO-09-19-0337-R<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">15. Virus-virus interactions in a plant host and in a hemipteran vector: Implications for vector fitness and virus epidemics<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam, S<sup>\u2020<\/sup>, Gadhave, KR<sup>\u2020<\/sup>, Buck, JW, Dutta, B, Coolong, T, Adkins, S &amp; Srinivasan, R. (2020). Virus-virus interactions in a plant host and in a hemipteran vector: Implications for vector fitness and virus epidemics. <em>Virus Research<\/em>. <a href=\"https:\/\/doi.org\/10.1016\/j.virusres.2020.198069\">https:\/\/doi.org\/10.1016\/j.virusres.2020.198069<\/a>.<sup>\u2020<\/sup>Equal contribution<\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">14. A CRISPR\/dCas9 toolkit for functional analysis of maize genes<\/summary><div class=\"gb-accordion-text\">\n<p>Gentzel, IN, Park, CH, Bellizzi, M, Xiao, G, Gadhave, KR, Murphree, C, Yang, Q, LaMantia, J, Redinbaugh, MG, Balint-Kurti, P, Sit, T &amp; Wang, G-L. (2020). A CRISPR\/dCas9 toolkit for functional analysis of maize genes. <em>Plant Methods<\/em>. <a href=\"https:\/\/doi.org\/10.1186\/s13007-020-00675-5\">https:\/\/doi.org\/10.1186\/s13007-020-00675-5<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">13. Specific and spillover effects on vectors following infection of two RNA viruses in pepper plants<\/summary><div class=\"gb-accordion-text\">\n<p>Gautam, S, Mugerwa, H, Sundaraj, S, Gadhave, KR, Murphy, JF, Dutta, B &amp; Srinivasan, R. (2020). Specific and spillover effects on vectors following infection of two RNA viruses in pepper plants. <em>Insects. <\/em><a href=\"https:\/\/doi.org\/10.3390\/insects11090602\">https:\/\/doi.org\/10.3390\/insects11090602<\/a>.<\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2019<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">12. A non-persistent aphid transmitted <em>Potyvirus<\/em> differentially alters the fitness of its vector and non-vector<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR*, Dutta, B, Coolong, T &amp; Srinivasan, R. (2019). A non-persistent aphid transmitted <em>Potyvirus<\/em> differentially alters the fitness of its vector and non-vector. <em>Scientific Reports. <\/em><a href=\"https:\/\/doi.org\/10.1038\/s41598-019-39256-5\">https:\/\/doi.org\/10.1038\/s41598-019-39256-5<\/a>.<\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2018<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">11. Soil inoculation with <em>Bacillus<\/em> spp. modifies root endophytic bacterial diversity, evenness, and community composition in a context-specific manner<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR<sup>\u2020<\/sup>, Devlin, PF<sup>\u2020<\/sup>, Ebertz, A, Ross, A &amp; Gange, AC (2018). Soil inoculation with <em>Bacillus<\/em> spp. modifies root endophytic bacterial diversity, evenness, and community composition in a context-specific manner. <em>Microbial Ecology<\/em>. <a href=\"https:\/\/doi.org\/10.1007\/s0024\">https:\/\/doi.org\/10.1007\/s0024<\/a>. <sup>\u2020<\/sup>Equal contribution.<\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">10. Plant growth promoting rhizobacteria promote plant size inequality<\/summary><div class=\"gb-accordion-text\">\n<p>Gange, AC &amp; Gadhave, KR (2018). Plant growth promoting rhizobacteria promote plant size inequality. <em>Scientific Reports<\/em>. <a href=\"https:\/\/doi.org\/10.1038\/s41598-018-32111-z\">https:\/\/doi.org\/10.1038\/s41598-018-32111-z<\/a>.<\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">9. Interactions involving rhizobacteria and foliar feeding insects<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR* &amp; Gange, AC (2018). Interactions involving rhizobacteria and foliar feeding insects. In: Ohgushi, T., Wurst, S., Johnson, S. Aboveground-Belowground Community Ecology. Springer Publishing Company, NY. <a href=\"https:\/\/doi.org\/10.1007\/978-3-319-91614-9_6\">https:\/\/doi.org\/10.1007\/978-3-319-91614-9_6<\/a>.<\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2017<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">8. First Report of a <em>Cucurbit yellow stunting disorder virus <\/em>in cucurbits in Georgia, United States<\/summary><div class=\"gb-accordion-text\"><\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">7. Plasticity in host plant utilization by two host-associated lineages of <em>Aphis gossypii<\/em> Glover<\/summary><div class=\"gb-accordion-text\">\n<p>Barman, AK, Gadhave, KR, Dutta, B &amp; Srinivasan, R. (2017). Plasticity in host plant utilization by two host-associated lineages of <em>Aphis gossypii<\/em> Glover. <em>Bulletin of Entomological Research<\/em>. <a href=\"https:\/\/doi.org\/10.1094\/PHP-03-17-0016-BR\"><\/a><a href=\"https:\/\/doi:10.1017\/S0007485317000852\">https:\/\/doi:10.1017\/S0007485317000852<\/a>.<\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2016<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">6. Developing soil microbial inoculants for pest management: Can one have too much of a good thing?<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR*, Hourston, J &amp; Gange, AC. (2016). Developing soil microbial inoculants for pest management: Can one have too much of a good thing? <em>Journal of Chemical Ecology<\/em> 42: 348-356. <a href=\"https:\/\/doi.org\/10.1007\/s10886-016-0689-8\">https:\/\/doi.org\/10.1007\/s10886-016-0689-8<\/a> <\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2015<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">5. Plant growth-promoting <em>Bacillus<\/em> suppress <em>Brevicoryne brassicae<\/em> field infestation &amp; trigger density-dependent &amp; density-independent natural enemy responses<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR*, Finch, P, Gibson, TM &amp; Gange, AC. (2015). Plant growth-promoting <em>Bacillus<\/em> suppress <em>Brevicoryne brassicae<\/em> field infestation &amp; trigger density-dependent &amp; density-independent natural enemy responses. <em>Journal of Pest Science<\/em>. <a href=\"https:\/\/doi.org\/10.1007\/s10340-015-0721-8\">https:\/\/doi:10.1007\/s10340-015-0721-8.<\/a><\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">4. <em>Bacillus<\/em> spp. alter the life history traits of the specialist, <em>Brevicoryne brassicae<\/em> L.<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR* &amp; Gange, AC. (2015). <em>Bacillus<\/em> spp. alter the life history traits of the specialist, <em>Brevicoryne brassicae<\/em> L. <em>Agricultural &amp; Forest Entomology<\/em> 18: 35-42. <a href=\"https:\/\/doi.org\/10.1111\/afe.12131\">https:\/\/doi.org\/10.1111\/afe.12131<\/a><\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2014<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">3. Characterization of secondary metabolites of an endophytic fungus from <em>Curcuma wenyujin<\/em><\/summary><div class=\"gb-accordion-text\">\n<p>Yan, J, Qi, N, Wang, S, Gadhave, KR, Zhao, J &amp; Yang, S. (2014). Characterization of secondary metabolites of an endophytic fungus from <em>Curcuma wenyujin<\/em>. <em>Current Microbiology<\/em> 69: 740-744. <a href=\"https:\/\/doi.org\/10.1007\/s00284-014-0647-z\">https:\/\/doi.org\/10.1007\/s00284-014-0647-z<\/a><\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h3 class=\"wp-block-heading\">2009<\/h3>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">2. Characterization of gram-negative bacterial isolates from gut of few multivoltine silkworm breeds<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR, Thangamalar, A, Muthuswami, M &amp; Subramanian, S. (2009a). Characterization of gram-negative bacterial isolates from gut of few multivoltine silkworm breeds. <em>Kar Agric Sci.<\/em> 22: 517-518.<\/p>\n<\/div><\/details><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">1. Use of 16S rRNA probes for characterization of gut microflora of silkworm (<em>Bombyx mori<\/em> L.) breeds<\/summary><div class=\"gb-accordion-text\">\n<p>Subramanian, S, Gadhave, KR, Mohanraj, P &amp; Thangamalar, A. (2009b). Use of 16S rRNA probes for characterization of gut microflora of silkworm (<em>Bombyx mori<\/em> L.) breeds. <em>Kar Agric Sci.<\/em> 22: 476-478.<\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-container gb-block-container\"><div class=\"gb-container-inside\"><div class=\"gb-container-content\">\n<h2 class=\"wp-block-heading\"><strong>Non-peer-reviewed<\/strong><\/h2>\n\n\n\n<div class=\"wp-block-genesis-blocks-gb-accordion gb-block-accordion\"><details><summary class=\"gb-accordion-title\">1. The Curious Case of the Large Blue Butterfly &#8211; a Conservation Success Story<\/summary><div class=\"gb-accordion-text\">\n<p>Gadhave, KR. (2014). <a href=\"https:\/\/entomologytoday.org\/2014\/04\/04\/the-curious-case-of-the-large-blue-butterfly-a-conservation-success-story\/\">The Curious Case of the Large Blue Butterfly &#8211; a Conservation Success Story<\/a>. In: <em>Entomology Today<\/em> (ed. Levine, R). Entomological Society of America.<\/p>\n<\/div><\/details><\/div>\n<\/div><\/div><\/div>\n\n\n\n<hr class=\"wp-block-separator has-css-opacity is-style-default fade-in-up\" \/>\n<\/div><\/div><\/div>\n","protected":false},"excerpt":{"rendered":"","protected":false},"author":30,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"_uag_custom_page_level_css":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_genesis_hide_title":true,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":"","footnotes":""},"class_list":{"0":"post-86","1":"page","2":"type-page","3":"status-publish","5":"entry"},"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO 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