Functional characterization of RhuB as a second TonB2-dependent hemin receptor in Riemerella anatipestifer CH-1

Author:

Wang Mengying1234ORCID,Wang Siyi1234,Wang Mingshu1234,Zhu Dekang1234ORCID,Jia Renyong1234ORCID,Chen Shun1234,Zhao Xinxin1234,Yang Qiao1234,Wu Ying1234,Zhang Shaqiu1234,Huang Juan1234,Liu Mafeng1234ORCID,Cheng Anchun1234ORCID

Affiliation:

1. Engineering Research Center of Southwest Animal Disease Prevention and Control Technology, Ministry of Education of the People’s Republic of China, Chengdu, China

2. Key Laboratory of Animal Disease and Human Health of Sichuan Province, Chengdu, China

3. International Joint Research Center for Animal Disease Prevention and Control of Sichuan Province, Chengdu, China

4. Research Center of Avian Disease, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, China

Abstract

ABSTRACT In the previous study, it was shown that Riemerella anatipestifer ( R. anatipestifer , RA), a pathogen in ducks and some other birds, encodes a hemin uptake system. The R. anatipestifer hemin uptake receptor RhuR is a TonB2-dependent hemin transporter. However, it remains unclear whether R. anatipestifer encodes additional TonB-dependent hemin transporters. Herein, we demonstrated that R. anatipestifer hemin uptake receptor B (RhuB) of R. anatipestifer CH-1 (RA CH-1) was negatively regulated by iron and mediated by the Fur protein, and knocking out rhuB damaged the ability of RA CH-1 to utilize iron from duck hemoglobin (Hb) but not that from duck serum. Moreover, the ability to use iron from Hb was restored by the expression rhuB in trans . Furthermore, the RhuB of RA CH-1 is a membrane protein, and recombinant RhuB could bind hemin at a 1:1 molar ratio in vitro . Compared to that of Δ tonB1 Δ rhuR , the ability of Δ tonB1 Δ rhuR Δ rhuB to utilize hemin was impaired; meanwhile, compared to that of Δ tonB2 Δ rhuR , the hemin utilization ability of Δ tonB2 Δ rhuR Δ rhuB was not affected, indicating that RhuB is a TonB2-dependent receptor. Compared to Δ rhuB , ΔrhuBΔrhuA did not affect hemin utilization. However, compared to Δ rhuA , ΔrhuBΔrhuA had reduced ability to utilize hemin, suggesting that RhuA relies on RhuB for its activity. Finally, the deletion of rhuB did not affect the virulence of RA CH-1. These results suggested that RhuB encodes a TonB2-dependent hemin receptor. The characterization of the second TonB-dependent receptor in R. anatipestifer enriches our understanding of the hemin uptake system of this bacterium. IMPORTANCE Iron is essential for the survival of most bacteria, and hemin of hemoglobin can serve as an important iron source. In our previous studies, we showed that R. anatipestifer CH-1 encodes a TonB2-dependent hemin receptor RhuR, which is involved in hemin uptake. The deletion of rhuR did not abolish hemin utilization by RA CH-1. We hypothesized that additional hemin uptake systems exist in this bacterium. In this study, we identified the second TonB2-dependent hemin receptor RhuB in RA CH-1 through hemin utilization, protein localization, and hemin-binding experiments. The duck infection model showed that the deletion of rhuB did not affect the virulence of RA CH-1. This study is not only important for further understanding the hemin utilization mechanism of R. anatipestifer , but also for enriching the hemin uptake transporters of gram-negative bacteria.

Funder

MOST | National Natural Science Foundation of China

SPDST | Natural Science Foundation of Sichuan Province

MOA | Earmarked Fund for China Agriculture Research System

China's Agricultural Research System | Sichuan Veterinary Medicine and Drug Innovation Group of China Agricultural Research System

Publisher

American Society for Microbiology

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