# New Mexico IDeA Networks of Biomedical Research Excellence (INBRE)

> **NIH NIH P20** · NEW MEXICO STATE UNIVERSITY LAS CRUCES · 2024 · $635,073

## Abstract

PROJECT SUMMARY
 Vibrio cholerae, the causative agent of the diarrheal
disease cholera, forms biofilm aggregates in the host
intestinal crypts that are critical to disease pathogenesis.
One factor that affects V. cholerae virulence and biofilm
formation is the sensing of nitric oxide (NO), an important
mediator of host immune defense. Intestinal infection with
V. cholerae causes upregulation of inducible NO synthase
in the intestinal epithelium and in intestinal macrophages.
This in turn leads to elevated NO levels in the intestinal
lumen where V. cholerae resides. A better understanding
of the mechanisms involved in V. cholerae's response to
NO is important, since common therapeutics used in
cholera treatment alter host production of NO. V. cholerae
can sense and respond to NO through two major NO-
sensing proteins: Heme nitric oxide/oxygen binding protein Fig. 1. Overview of the project and the collaborative team.
(H-NOX) and NO-sensing protein (NosP). Intriguingly, H-
NOX is thought to promote biofilm formation through indirect inhibition of a phosphodiesterase (PDE), while
NosP is thought to favor biofilm dissolution by inhibition of the quorum sensing histidine kinase (HK) VpsS.
How the two V. cholerae NO-sensors (H-NOX and NosP) in combination affect biofilm formation and
virulence during infection of the host intestinal epithelium is unclear.
 Addressing the complex interplay between host NO production, V. cholerae NO-sensing, NO signaling
pathways, biofilm formation, and the resulting host response requires complementary expertise in mucosal
immunobiology, bacterial signaling pathways, and biofilms. We have assembled a multi-disciplinary team of
mid-career PIs from three INBRE states to undertake this work. The focus of our project on NO-sensing and
biofilm formation in V. cholerae will enable all three PIs to apply their expertise to a new area of investigation
while developing a highly synergistic collaborative project. Dr. Tseng at the University of Nevada Las Vegas
(UNLV) will contribute biofilm expertise that she has gained in studies on Pseudomonas aeruginosa. Dr.
Bimczok at Montana State University (MSU) will contribute her expertise in organoid-immune cell co-culture
models of infection that she has gained in her research on gastric H. pylori infection. Dr. Yukl at New Mexico
State University (NMSU) will contribute his expertise on bacterial NO sensing systems and extend his work to
define relevant signaling pathways downstream of the NO sensors (Fig. 1).
 For this team development project, we aim to, first, establish and validate our experimental model systems,
second, generate preliminary data, and third, strengthen our collaborative interactions. With our proposed
experiments, we will (1) assess in vitro biofilm formation phenotypes of V. cholerae NO-sensing mutants
(Tseng); (2) elucidate how sensing of epithelial and macrophage-derived NO by V. cholerae impacts biofilm
formation and virulence in the context of host cells (Bimc...

## Key facts

- **NIH application ID:** 11046440
- **Project number:** 3P20GM103451-24S2
- **Recipient organization:** NEW MEXICO STATE UNIVERSITY LAS CRUCES
- **Principal Investigator:** SHELLEY LUSETTI
- **Activity code:** P20 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $635,073
- **Award type:** 3
- **Project period:** 2001-09-30 → 2029-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/11046440

## Citation

> US National Institutes of Health, RePORTER application 11046440, New Mexico IDeA Networks of Biomedical Research Excellence (INBRE) (3P20GM103451-24S2). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/11046440. Licensed CC0.

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