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Severns, P.

Publications and source records attributed to Severns, P..

2 recordsLinked to original sources

Elucidating the patterns of seed-to-seedling transmission of Xanthomonas citri pv. malvacearum, the causal agent of cotton bacterial blight

Cotton bacterial blight (CBB) was a major disease of cotton in the United States in the early part of the 20th century. The recent reemergence of CBB, caused by Xanthomonas citri pv. malvacearum (Xcm) revealed many gaps in our understanding of this important disease. In this study, we employed a field isolate of Xcm from Georgia USA (WT) to generate a non- pathogenic, hrcV mutant lacking a functional Type III Secretion System (T3SS-). We tagged the WT and T3SS- strains with an auto-bioluminescent Tn7 reporter and compared colonization patterns of susceptible and resistant cotton seedlings using macroscopic image analysis and bacterial load enumeration. Wildtype and T3SS- Xcm strains colonized cotton cotyledons of resistant and susceptible cotton cultivars. However, Xcm populations were significantly higher in susceptible seedlings inoculated with the WT strain. Additionally, WT and T3SS- Xcm strains systemically colonized true leaves, although at different rates. Finally, we observed that seed-to-seedling transmission of Xcm may involve systemic spread through the vascular tissue of cotton plants. These findings yield novel insights into potential Xcm reservoirs for CBB outbreaks.

plant biology

The distribution of onion virulence gene clusters among Pantoea spp.

Pantoea ananatis is a gram-negative bacterium and the primary causal agent of center rot of onions in Georgia. Previous genomic studies identified two virulence gene clusters, HiVir and alt, associated with center rot. The HiVir gene cluster is required to induce necrosis on onion tissues via synthesis of a predicted small molecule toxin. The alt gene cluster aids in tolerance to thiosulfinates generated during onion tissue damage. Whole genome sequencing of other Pantoea species suggest that these gene clusters are present outside of P. ananatis. To assess the distribution of these gene clusters, two PCR primer sets were designed to detect the presence of HiVir and alt. Two hundred fifty-two strains of Pantoea spp. were phenotyped using the red onion scale necrosis (RSN) assay and were assayed using PCR for the presence of these virulence genes. A diverse panel of strains from three distinct culture collections comprised of 24 Pantoea species, 41 isolation sources, and 23 countries, collected from 1946-2019, were tested. There is a significant association between the alt PCR assay and Pantoea strains recovered from symptomatic onion (P<0.001). There is also a significant association of a positive HiVir PCR and RSN assay among P. ananatis strains but not among Pantoea spp., congeners. This may indicate a divergent HiVir cluster or different pathogenicity and virulence mechanisms. Last, we describe natural alt positive [RSN+/HiVir+/alt+] P. ananatis strains, which cause extensive bulb necrosis in a neck-to-bulb infection assay compared to alt negative [RSN+/HiVir+/alt-] P. ananatis strains. A combination of assays that include PCR of virulence genes [HiVir and alt] and an RSN assay can potentially aid in identification of onion-bulb-rotting pathogenic P. ananatis strains.

plant biology