At the onset of bacterial chromosome replication initiation, replicative helicases are loaded onto DNA, a process requiring helicase loaders. While organisms documented as lacking a helicase loader are rare, the human pathogen Helicobacter pylori is a notable exception. Here, relying mainly on genomic synteny and AlphaFold, I demonstrate that the well-documented helicase loader gene dciA is present in the H. pylori genome and co-localizes with the uvrC gene (excinuclease ABC subunit C), which highlights the limitations of the usual methodology used to identify dciA . I then provide evidence showing that this finding seriously challenges the two main current chromosome replication initiation models in this bacterium. Given that virulent strains of H. pylori pose a significant threat to human health, contributing to various gastric and non-gastric disorders, including certain cancers, I conclude that a deeper understanding of replication initiation in H. pylori could facilitate the development of more effective therapeutic strategies.
Pierre Brézellec (Wed,) studied this question.