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Stumpf, C.

Publications and source records attributed to Stumpf, C..

2 recordsLinked to original sources

Regulator-derived growth and fitness costs of Salmonella SPI-2 expression are environment specific and T3SS independent

Bacterial pathogens must evolve regulatory mechanisms that balance the necessity of virulence genes with the costs associated with their expression. Salmonella Pathogenicity Island-2 (SPI-2) is a genomic locus that encodes a Type 3 Secretion System (T3SS) and secreted effectors necessary for intracellular survival and replication. Recent work has shown that SPI-2 is expressed heterogeneously, suggesting uniform or aberrant expression of the system carries fitness costs. Here, we report a negative correlation between microcolony growth and SPI-2 expression, suggesting a growth cost to expression of SPI-2. To quantify and mechanistically evaluate this cost, we employ knockout and synthetic expression of the SPI-2 master regulator ssrB to eliminate or force the expression of SPI-2 genes. We find that ssrB expression causes deficits throughout the growth curve and puts cells at a competitive disadvantage in acidic, nutrient limited media. We further show that these deficits are environment specific, and not observed until stationary phase in neutral, rich media. We also observe unexpected cell morphology effects of ssrB expression, suggesting its effects on the cell extend beyond its regulation of SPI-2 genes. Using known ssrB mutations we find that DNA-binding activity, but not phosphorylation, of SsrB is necessary for growth costs. Lastly, we show that this growth cost is incurred even in the absence of the SPI-2 genetic locus, indicating that it is inherent to expression of ssrB, rather than its primary downstream virulence gene targets. These results demonstrate that SPI-2 expression is coupled to context specific cell growth and fitness deficits induced by its master regulator, offering a potential benefit to heterogeneous expression. SIGNIFICANCEVirulence factors are often heterogeneously expressed in bacteria, offsetting the resource and energetic burdens they impose. Characterizing such burdens reveals the evolutionary pressures that act on virulence genes and uncovers the logic behind regulatory mechanisms that drive heterogeneity in their expression. This study evaluates the growth and fitness costs associated with expression of Salmonella Pathogenicity Island-2 (SPI-2), which encodes a Type 3 Secretion System and secreted effectors required for intracellular survival and replication. The expression of the SPI-2 master regulator ssrB is shown to impose environment-specific growth and fitness deficits. These deficits persist in the absence of T3SS genes, suggesting that costs originate from SsrB acting on other target genes. These results provide critical context to recent observations of heterogeneous SPI-2 expression, elucidating the fitness cost this heterogeneity has evolved to offset.

microbiology↗

Circulating Immune Cells are Associated with Non-Inflammatory Pain in Rheumatoid Arthritis

Over half of patients with rheumatoid arthritis (RA) report clinically meaningful pain, despite treatment with disease-modifying antirheumatic drugs (DMARDs). While joint inflammation is a known cause of pain in patients with rheumatic diseases, emerging data indicate that many patients also suffer from centralized or nociplastic pain. There is a critical unmet need to characterize the altered cellular state that distinguishes patients with centralized pain. In the IMPACT study, 39 RA patients with minimal joint inflammation but varying levels of pain underwent quantitative sensory testing (QST) to assess nociplastic pain, completed patient-reported outcome (PRO) surveys, and provided blood samples for immune profiling. Supervised and unsupervised analysis of the multi-parameter spectral flow cytometry data identified immune cell populations correlated with nociplastic pain and patient-reported pain intensity. Moreover, analyses of single-cell RNA-seq from a subset of 22 patients revealed differences in cell type proportions and differential expression between the high and low pain groups. These studies provide novel insights into the role of circulating immune cells in altered central nervous system (CNS) pain regulation in adults with RA.

immunology↗