Translocation of YopJ family effector proteins through the VirB/VirD4 T4SS of Bartonella
The evolutionary conserved YopJ family comprises numerous type-III-secretion system (T3SS) effectors of diverse mammalian and plant pathogens that acetylate host proteins to dampen immune responses. Acetylation is mediated by a central acetyltransferase domain that is flanked by conserved regulatory sequences, while a non-conserved N-terminal extension encodes the T3SS-specific translocation signal. Bartonella spp. are facultative-intracellular pathogens causing intra-erythrocytic bacteremia in their mammalian reservoirs and diverse disease manifestations in incidentally infected humans. Bartonellae do not encode a T3SS, but most species possess a type-IV-secretion system (T4SS) to translocate Bartonella effector proteins (Beps) into host cells. Here we report that the YopJ homologs present in Bartonellae species represent genuine T4SS effectors. Like YopJ family T3SS effectors of mammalian pathogens, the Bartonella YopJ-like effector A (ByeA) of Bartonella taylorii also targets MAP kinase signaling to dampen pro-inflammatory responses, however, translocation depends on a functional T4SS. A split-NanoLuc luciferase-based translocation assay identified sequences required for T4SS-dependent translocation in conserved regulatory regions at the C-terminus and proximal to the N-terminus of ByeA. The T3SS effectors YopP from Yersinia enterocolitica and AvrA from Salmonella Typhimurium were also translocated via the Bartonella T4SS, while ByeA was not translocated via the Yersinia T3SS. Our data suggest that YopJ family T3SS effectors may have evolved from an ancestral T4SS effector, such as ByeA of Bartonella. In this evolutionary scenario, the signal for T4SS-dependent translocation encoded by N- and C-terminal sequences remained functional in the derived T3SS effectors due to the essential role these sequences coincidentally play in regulating acetyltransferase activity. Significance StatementBacterial pathogens use diverse secretion systems to translocate effector proteins into eukaryotic host cells. Evolutionary successful translocation systems and effector proteins have been acquired by many plant and animal pathogens via horizontal gene transfer. The YopJ family comprises numerous T3SS effectors that share a unique acetyltransferase activity that interferes with various host cell functions. Our study revealed that YopJ homologs in the pathogen Bartonella are genuine T4SS effectors and implies an evolutionary scenario in which T3SS-dependent YopJ family effectors may have evolved from such an ancestral T4SS effector by fusion of an N-terminal type-III-secretion signal. Such switches in secretion system specificity of host-targeted effectors may represent an underappreciated phenomenon in effector evolution.