Phylogenetic distribution and evolutionary dynamics of and T3SS genes in the genus .

Microb Genom

Department of Infectious Disease Epidemiology. Imperial College London, St Mary's Hospital Campus, Praed Street, London W2 1NY, UK.

Published: September 2020


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Article Abstract

are abundant soil bacteria and the major symbiont of legumes. The recent availability of genome sequences provides a large source of information for analysis of symbiotic traits. In this study, we investigated the evolutionary dynamics of the nodulation genes () and their relationship with the genes encoding type III secretion systems (T3SS) and their effectors among bradyrhizobia. Based on the comparative analysis of 146 genome sequences, we identified six different types of T3SS gene clusters. The two predominant cluster types are designated RhcIa and RhcIb and both belong to the RhcI-T3SS family previously described in other rhizobia. They are found in 92/146 strains, most of them also containing genes. RhcIa and RhcIb gene clusters differ in the genes they carry: while the translocon-encoding gene is systematically found in strains containing RhcIb, the and genes are specifically conserved in strains containing RhcIa, suggesting that these last two genes might functionally substitute and play a role related to effector translocation. Phylogenetic analysis suggests that bradyrhizobia simultaneously gained and RhcI-T3SS gene clusters via horizontal transfer or subsequent vertical inheritance of a symbiotic island containing both. Sequence similarity searches for known Nop effector proteins in bradyrhizobial proteomes revealed the absence of a so-called core effectome, i.e. that no effector is conserved among all strains. However, NopM and SUMO proteases were found to be the main effector families, being represented in the majority of the genus. This study indicates that bradyrhizobial T3SSs might play a more significant symbiotic role than previously thought and provides new candidates among T3SS structural proteins and effectors for future functional investigations.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643967PMC
http://dx.doi.org/10.1099/mgen.0.000407DOI Listing

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