Laribacter hongkongensis anaerobic adaptation mediated by arginine metabolism is controlled by the cooperation of FNR and ArgR. (22nd January 2017)

• Record Type: Journal Article
• Authors: Xiong, Lifeng; Yang, Ying; Ye, Yuan‐Nong; Teng, Jade L. L.; Chan, Elaine; Watt, Rory M.; Guo, Feng‐Biao; Lau, Susanna K. P.; Woo, Patrick C. Y.
• Other Names: Hallsworth John E. guestEditor.
• Is Part Of: Environmental microbiology. Volume 19:Number 3(2017:Mar.)
• Page Start: 1266
• Page End: 1280
• Publication Date: 2017-01-22
• Subjects: Microbial ecology -- Periodicals; Environmental Microbiology -- Periodicals; 579.17
• DOI: 10.1111/1462-2920.13657
• Languages: English
• ISSNs: 1462-2912

Abstract

Summary: Laribacter hongkongensis is a fish‐borne pathogen associated with invasive infections and gastroenteritis. Its adaptive mechanisms to oxygen‐limiting conditions in various environmental niches remain unclear. In this study, we compared the transcriptional profiles of L. hongkongensis under aerobic and anaerobic conditions using RNA‐sequencing. Expression of genes involved in arginine metabolism significantly increased under anoxic conditions. Arginine was exploited as the sole energy source in L. hongkongensis for anaerobic respiration via the arginine catabolism pathway: specifically via the arginine deiminase (ADI) pathway. A transcriptional regulator FNR was identified to coordinate anaerobic metabolism by tightly regulating the expression of arginine metabolism genes. FNR executed its regulatory function by binding to FNR boxes in arc operons promoters. Survival of isogenic fnr mutant in macrophages decreased significantly when compared with wild‐type; and expression level of fnr increased 8 h post‐infection. Remarkably, FNR directly interacted with ArgR, another regulator that influences the biological fitness and intracellular survival of L. hongkongensis by regulating arginine metabolism genes. Our results demonstrated that FNR and ArgR work in coordination to respond to oxygen changes in both extracellular and intracellular environments, by finely regulating the ADI pathway and arginine anabolism pathways, thereby optimizing bacterial fitness in various environmental niches.