Structural and regulatory mutations in Vibrio parahaemolyticus type III secretion systems display variable effects on virulence. Issue 2 (1st December 2014)

• Record Type: Journal Article
• Authors: Calder, Thomas; de Souza Santos, Marcela; Attah, Victoria; Klimko, John; Fernandez, Jessie; Salomon, Dor; Krachler, Anne-Marie; Orth, Kim
• Is Part Of: FEMS microbiology letters. Volume 361:Issue 2(2014:Dec.)
• Page Start: 107
• Page End: 114
• Publication Date: 2014-12-01
• Subjects: T3SS -- Vibrio parahaemolyticus -- bacterial virulence -- invasion -- biofilm; Microbiology -- Periodicals; 579
• DOI: 10.1111/1574-6968.12619
• Languages: English
• ISSNs: 0378-1097

Abstract

Abstract: The Gram-negative bacterium, Vibrio parahaemolyticus, is a major cause of seafood-derived food poisoning throughout the world. The pathogenicity of V. parahaemolyticus is attributed to several virulence factors, including two type III secretion systems (T3SS), T3SS1 and T3SS2. Herein, we compare the virulence of V. parahaemolyticus POR strains, which harbor a mutation in the T3SS needle apparatus of either system, to V. parahaemolyticus CAB strains, which harbor mutations in positive transcriptional regulators of either system. These strains are derived from the clinical RIMD 2210633 strain. We demonstrate that each mutation affects the virulence of the bacterium in a different manner. POR and CAB strains exhibited similar levels of swarming motility and T3SS effector production and secretion, but the CAB3 and CAB4 strains, which harbor a mutation in the T3SS2 master regulator gene, formed reduced biofilm growth under T3SS2 inducing conditions. Additionally, while the cytotoxicity of the POR and CAB strains was similar, the CAB2 (T3SS1 regulatory mutant) strain was strikingly more invasive than the comparable POR2 (T3SS1 structural mutant) strain. In summary, creating structural or regulatory mutations in either T3SS1 or T3SS2 causes differential downstream effects on other virulence systems. Understanding the biological differences of strains created from a clinical isolate is critical for interpreting and understanding the pathogenic nature of V. parahaemolyticus . We demonstrate that structural or regulatory mutations of V. parahaemolyticus type III secretion systems cause downstream effects on other virulence systems, which uncovers an interconnected relationship between these systems. We demonstrate that structural or regulatory mutations of V. parahaemolyticus type III secretion systems cause downstream effects on other virulence systems, which uncovers an interconnected relationship between these systems.