Abstract

Riemerella anatipestifer is a duck pathogen that has caused serious economic losses to the duck industry worldwide. Despite this, there are few reported studies of the physiological and pathogenic mechanisms of Riemerella anatipestifer infection. In previous study, we have shown that TonB1 and TonB2 were involved in hemin uptake. TonB family protein (TbfA) was not investigated, since knockout of this gene was not successful at that time. Here, we used a plasmid based gene over-expression and knockdown to investigate its function. First, we constructed three Escherichia-Riemerella anatipestifer shuttle vectors containing three different native Riemerella anatipestifer promoters. The shuttle plasmids were introduced into Riemerella anatipestifer ATCC11845 by conjugation at an efficiency of 5 × 10−5 antibiotic-resistant transconjugants per recipient cell. Based on the high-expression shuttle vector pLMF03, a method for gene knockdown was established. Knockdown of TbfA in Riemerella anatipestifer ATCC11845 decreased the organism’s growth ability in TSB medium but did not affect its hemin utilization. In contrast, over-expression of TbfA in Riemerella anatipestifer ATCC11845ΔtonB1ΔtonB2. Significantly promoted the organism’s growth in TSB medium but significantly inhibited its hemin utilization. Collectively, these findings suggest that TbfA is not involved in hemin utilization by Riemerella anatipestifer.

Highlights

  • We identified the functions held by ExbB-ExbD-TonB (TonB1 system) encoded by RA0 C_1191-RA0C_1192-RA0C_1193, ExbB-ExbD-ExbD-TonB (TonB2 system) encoded by RA0C_1212-RA0C_ 1211-RA0C_1210-RA0C_1209, and a TonB family protein (TbfA) encoded by RA0C_0334, in R. anatipestifer ATCC118452

  • TbfA is not linked with exbB-exbD genes, and it would unlikely be involved in iron/hemin transport

  • The results showed that the cfx gene could be amplified from all isolated clones and isolated plasmids pLMF01, demonstrating that this plasmid can stably replicate in R. anatipestifer(data not shown)

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Summary

Introduction

We identified the functions held by ExbB-ExbD-TonB (TonB1 system) encoded by RA0 C_1191-RA0C_1192-RA0C_1193, ExbB-ExbD-ExbD-TonB (TonB2 system) encoded by RA0C_1212-RA0C_ 1211-RA0C_1210-RA0C_1209, and a TonB family protein (TbfA) encoded by RA0C_0334, in R. anatipestifer ATCC118452. Hemin transport is nearly abolished only when both tonB1 and tonB2 are deleted, suggesting that both TonB1 and TonB2 are involved in hemin transport in R. anatipestifer and that they are functionally redundant[2]. To investigate the function of TbfA, we first constructed a series of E. coli-R. anatipestifer shuttle vectors based on plasmid pMM47. A15 and the putative replication region of plasmid pRA0726 of R. anatipestifer 072616. These vectors could be used for gene over-expression and gene knockdown in R. anatipestifer strains. Using these methods, we showed that the TbfA protein in R. anatipestifer ATCC11845 is not involved in hemin utilization but is required for optimal growth

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