Judith K Brown

Judith K Brown

Professor, Plant Science
Regents Professor, Plant Sciences
Research Associate Professor, Entomology
Professor, Entomology / Insect Science - GIDP
Professor, BIO5 Institute
Member of the General Faculty
Member of the Graduate Faculty
Primary Department
Department Affiliations
Contact
(520) 621-1402

Work Summary

Unravel the phylodynamics and transmission-specific determinants of emerging plant virus/fastidious bacteria-insect vector complexes, and translate new knowledge to abate pathogen spread in food systems.

Research Interest

Judith Brown, PhD, and her research interests include the molecular epidemiology of whitefly-transmitted geminiviruses (Begomoviruses, Family: Geminiviridae), the basis for virus-vector specificity and the transmission pathway, and the biotic and genetic variation between populations of the whitefly vector, B. tabaci, that influence the molecular epidemiology and evolution of begomoviruses. Keywords: Plant viral genomics, emergent virus phylodynamics, functional genomics of insect-pathogen interactions

Publications

Cicero, J. M., & Brown, J. K. (2011). Functional anatomy of whitefly organs associated with Squash leaf curl virus (Geminiviridae: Begomovirus) transmission by the B biotype of Bemisia tabaci (Hemiptera: Aleyrodidae). Annals of the Entomological Society of America, 104(2), 261-279.

Abstract:

The sweetpotato whitefly, Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae), is a sibling species group that transmits Squash leaf curl virus (SLCV) and other geminiviruses (Geminiviridae, genus Begomovirus) in a circulative and persistent manner. Using in situ hybridization, SLCV was localized in the primary salivary glands, the midgut, and the filter chamber of adults of the B biotype in the group. However, no SLCV particles were localized in the accessory salivary glands. The midgut loop was found to reside, fully or partially, in the abdomen or thorax in >8,000 dissections, indicating that it is capable of moving through the petiole, a constriction between the two body sections. When extended to its anterior-most position in the thorax, the midgut can make direct contact with the salivary glands, but evidence for direct transfer of virions is lacking. However, the widely presumed pathway of viral transport from the gut to the whitefly primary salivary glands can now be broadened to include both the blood and the possibility of direct transfer during contiguity of these two organs. Light microscopical observations indicated that the primary salivary gland consists of a central region flanked by two dark-staining regions, referred to as endcaps. Electron microscopical examination of extirpated and nonextirpated primary salivary glands revealed additional distinct regions and cell types. One such region, located between the central region and an endcap, was correlated directly to the region where virions have previously been immunolocalized. © 2011 Entomological Society of America.

Papayiannis, L. C., Brown, J. K., Seraphides, N. A., Hadjistylli, M., Ioannou, N., & Katis, N. I. (2009). A real-time PCR assay to differentiate the B and Q biotypes of the Bemisia tabaci complex in Cyprus. Bulletin of Entomological Research, 99(6), 573-582.

PMID: 19203404;Abstract:

A real-time PCR assay based on TaqMan® technology was developed and evaluated for the rapid detection of the B and Q biotypes of Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). A survey was conducted during 2005-2007 in order to identify the distribution and prevalence of B. tabaci biotypes in Cyprus using the real-time PCR assay. More than 700 adult whiteflies collected from 35 cultivated and weed plant species were individually haplotyped using TaqMan® PCR, and the results of the assay were validated by restriction fragment length polymorphism analysis and DNA sequencing of the mitochondrial cytochrome oxidase I (mtCOI) gene. Two biotypes, B and Q, were identified in the collected plant species on the island. The real-time PCR and RFLP assay consistently yielded the same results, although the real-time assay was more sensitive and less time consuming. Phylogenetic analysis of the mtCOI DNA sequences corroborated the identity of the B and Q biotypes 100% of the time and by phylogenetic analysis the haplotypes grouped, as expected, in the major North African-Mediterranean-Middle Eastern clade of the B. tabaci complex. © 2009 Cambridge University Press.

Brown, J. K. (2014). Population structure of the greenhouse whitefly, Trialeurodes vaporariorum (Westwood), an invasive species from the Americas, 60 years after invading China. Int. J. Mol. Sci., 15, 13514-13528.

Gao, R.R., Zhang, W.P., Zhang, R.M., Zhou, H.X., Pan, H.P., Zhang, Y.J., Brown, J.K., and Chu, D. 2014. Population structure of the greenhouse whitefly, Trialeurodes vaporariorum (Westwood), an invasive species from the Americas, 60 years after invading China. Int. J. Mol. Sci. 15:13514-13528. doi:10.3390/ijms150813514.

Hernández-Zepeda, C., Brown, J. K., Moreno-Valenzuela, O., Argüello-Astorga, G., Idris, A. M., Carnevali, G., & Rivera-Bustamante, R. (2010). Characterization of Rhynchosia yellow mosaic Yucatan virus, a new recombinant begomovirus associated with two fabaceous weeds in Yucatan, Mexico. Archives of Virology, 155(10), 1571-1579.

PMID: 20574644;Abstract:

Rhynchosia minima (L.) DC. (Fabaceae) plants exhibiting bright golden mosaic symptoms were previously associated with begomovirus infection in Yucatan, México [1]. To characterize the begomovirus infecting these plants, the complete bipartite genome was cloned and sequenced. Sequence comparisons indicated that the virus was distinct from all other begomoviruses known to date, including those previously identified from symptomatic R. minima, and the name Rhynchosia yellow mosaic Yucatan virus (RhYMYuV) is proposed. Pairwise comparisons indicated that RhYMYuV DNA-A [2,597 nt, (EU021216)] and DNA-B [2,542 nt, (FJ792608)] components shared the highest nt sequence identity with Cabbage leaf curl virus (CaLCuV), 87% for component A and 71% for component B. Phylogenetic analysis indicated that both components of RhYMYuV are most closely related to other New World begomoviruses, having as closest relatives immediate outliers to the major Squash leaf curl virus (SLCV) clade. Recombination analysis of the RhYMYuV genome indicated that the DNA-A component has arisen through intermolecular recombination. R. minima plants inoculated with the monomeric clones developed a bright yellow mosaic similar to symptoms observed in naturally infected plants, confirming that the clones were infectious. Nicotiana benthamiana plants biolistically inoculated with monomeric clones developed curling and chlorosis in the newly emerging leaves. RhYMYuV was also detected in symptomatic Desmodium sect. Scorpiurus Benth. (Fabaceae) that were collected near the RhYMYuV-infected plants. © 2010 Springer-Verlag.

Cicero, J., & Brown, J. (2011). Functional anatomy of whitefly organs associated with Squash leaf curl virus (Geminiviridae: Begomovirus) transmission by the B Biotype of Bemisia tabaci (Aleyrodidae: Hemiptera). Ann. Entomol. Soc. Am, 104, 261-279.