Two mammalian-like cysteine dioxygenases and a sulfite exporter play important roles in sulfur homeostasis and virulence of a human pathogen
Bordetella pertussis is a strictly human, re-emerging respiratory pathogen and the causative agent of whooping cough. Through its adaptation to humans, B. pertussis decayed or lost genes of the sulfate assimilation pathway and, consequently, must obtain cysteine from the host. Previously, we showed that the sulfur metabolism of B. pertussis is substantially rewired during infection of human macrophages. Here, we investigated the role of several cysteine metabolism- and transport-related genes in the fitness and virulence of this pathogen. We show that excess cysteine strongly induces the expression of genes encoding two cysteine dioxygenases, BP2871 and BP3011, and a putative sulfite exporter, BP2808. The mutant lacking both cysteine dioxygenase genes exhibits impaired growth in vitro, severely reduced secretion of pertussis toxin, and attenuated virulence in vivo. We also demonstrate the essential role of the sulfite exporter BP2808 and {gamma}-glutamyl-cysteine synthase BP0598 in the adaptation of B. pertussis to stress induced by excess cysteine. Intriguingly, both cysteine dioxygenases contain cysteine near the active site, a feature typical of mammalian enzymes and associated with the capacity to increase CDO activity and stability in response to excess cysteine. We hypothesize that the presence of cysteine represents an evolutionary adaptation that improves the survival of B. pertussis within a mammalian host. Overall, our data suggest that sulfur metabolism has been effectively streamlined in B. pertussis and plays an important role at the host-pathogen interface. ImportanceSulfur is one of the essential nutrients required by cells for growth and cysteine is central to sulfur metabolism. While most bacteria prefer environmentally available sulfate as their cysteine source, several bacterial pathogens rely on cysteine provided by the host. Here we show that Bordetella pertussis, the causative agent of whooping cough, has simplified its sulfur metabolism. Our data suggest that two cysteine dioxygenases and sulfite exporter play key roles in sulfur homeostasis and redox balance. Both dioxygenases enable the pathogen to use cysteine as a source of sulfur and the sulfite exporter removes the toxic byproduct of cysteine conversion. Importantly, lack of cysteine dioxygenase activity leads to aberrant secretion of pertussis toxin, one of the essential virulence factors, resulting in attenuated virulence of the pathogen. We suggest that cysteine auxotrophy can be considered part of an infection strategy that assists B. pertussis in adapting to its human host.