Biology subjects

Ballard, M.

Publications and source records attributed to Ballard, M..

3 recordsLinked to original sources

bioRxiv2026

ORGANOTYPIC ENDOTHELIAL IDENTITY DETERMINES DIVERGENT MOLECULAR AND FUNCTIONAL RESPONSES TO LPS AND IL-6

ABSTRACT Endothelial cells (ECs) display marked vascular bed-specific heterogeneity, and their inflammation-induced activation is a central feature of vascular pathology. However, whether inflammatory responses are primarily shaped by intrinsic organotypic endothelial identity or by the inflammatory stimulus itself remains largely unknown. To address this question, we compared the temporal responses of brain- (hCMEC/D3), skin- (HMEC-1), and lung-derived (HuLEC-5a) human microvascular ECs to lipopolysaccharide (LPS) and interleukin-6 (IL-6/IL-6R). Across all conditions, endothelial origin was the dominant determinant of transcriptional variation, outweighing the effects of both the inflammatory stimulus and exposure time. Brain-, skin- and lung-derived ECs exhibited distinct basal inflammatory and innate immune gene expression programs and responded differently to both LPS and IL-6/IL-6R. LPS induced a rapid but largely transient response, whereas IL-6/IL-6R elicited more sustained inflammatory changes. Although transcriptional profiling identified a shared inflammatory signature across EC populations, most differentially expressed genes were vascular bed specific. These molecular differences translated into distinct functional outcomes: IL-6/IL-6R increased endothelial permeability and promoted more sustained metabolic adaptations, whereas LPS induced robust inflammatory activation without persistent barrier dysfunction. Collectively, these findings demonstrate that while inflammatory stimuli determine which signaling pathways are activated, intrinsic endothelial identity dictates the magnitude, kinetics, and functional consequences of the inflammatory response. Our results highlight the importance of incorporating vascular bed specificity into experimental models and the development of therapies targeting endothelial dysfunction and inflammation.

cell biology↗

bioRxiv2025

Biofilm Forming Capacity, Sanitizer Tolerance and Genetic Characterization of Persistent and Non-Persistent Listeria monocytogenes from Artisanal Cheese Processing Environments

Listeria monocytogenes is known to colonize food production environments and cross-contaminate finished foods. We investigated 30 L. monocytogenes collected from artisan cheese production facilities in Vermont from 2006-2008 for sanitizer tolerance, biofilm formation capacity, biofilm architecture, and tolerance to sanitizers of mature biofilms. Sixteen of these isolates represented a putatively persistent ribotype (DUP-1042B) found in one facility over two years. Isolates of the putatively persistent ribotype all aligned into ST191 and were 0-6 SNPs different, confirming they represented a persistent strain. We found no significant differences in sanitizer tolerance or crystal assay-based attachment capacity between persistent and non-persistent strains. However, using scanning electron microscopy, we found that isolates FML-10 and FML-19 formed substantially denser biofilms after 10 days on stainless steel. Ten-day old biofilms were highly resistant to sanitizers; neither quaternary ammonium nor sodium hypochlorite-based sanitizers achieved an EPA-recommended 6-log reduction. More EPS was found in low-nutrient biofilm conditions; thus, non-food contact surfaces in cheese environments may induce formation of biofilms with high sanitizer tolerance. Our results highlight the importance of regular environmental testing and strain typing for rapid detection of L. monocytogenes colonization attempts while they can still be removed without major renovations or equipment replacement. HighlightsO_LIIsolates from persistent ribotype DUP-1042B/ST191 were within 6 SNPs of each other C_LIO_LITwo isolates from ST191 made dense biofilms in nutrient rich conditions C_LIO_LIMore EPS was produced in nutrient-poor conditions C_LIO_LIMature biofilms of all isolates were highly resistant to QAC and SH sanitizers C_LI ImportanceThis study identifies strategies used by a set of persistently colonizing L. monocytogenes isolated from an artisanal cheese producer in Vermont, finding that some persistently colonizing isolates had high biofilm forming capacity, which may have contributed to their persistence.

microbiology↗

bioRxiv2023

The image-based ultrasonic cell shaking test

Mechanical signals play a vital role in cell biology and is a vast area of research. Thus, there is motivation to understand cell deformation and mechanobiological responses. However, the ability to controllably deform cells in the ultrasonic regime and test their response is a noted challenge throughout the literature. Quantifying and eliciting an appropriate stimulus has proven to be difficult, resulting in methods that are either too aggressive or oversimplified. Furthermore, the ability to gain a real-time insight into cell deformation and link this with the biological response is yet to be achieved. One application of this understanding is in ultrasonic surgical cutting, which is a promising alternative to traditional methods, but with little understanding of its effect on cells. Here we present the image based ultrasonic cell shaking test, a novel method that enables controllable loading of cells and quantification of their response to ultrasonic vibrations. Practically, this involves seeding cells on a substrate that resonates at ultrasonic frequencies and transfers the deformation to the cells. This is then incorporated into microscopic imaging techniques to obtain high-speed images of ultrasonic cell deformation that can be analysed using digital image correlation techniques. Cells can then be extracted after excitation to undergo analysis to understand the biological response to the deformation. This method could aid in understanding the effects of ultrasonic stimulation on cells and how activated mechanobiological pathways result in physical and biochemical responses.

bioengineering↗