LAUSR

Common ragweed (Ambrosia artemisiifolia) is one of the leading causes of allergenic rhinitis, as well as a major weed of many crops. Biological control with plant pathogens, such as fungi and bacteria, represents an attractive alternative to the application of synthetic herbicides to control this noxious weed. In this study, we isolated a Xanthomonas strain (designated as 10‐10) from a diseased common ragweed plant collected in southern Quebec, Canada. We characterized the bioherbicidal potential of this strain against common ragweed, and determined whether it can infect other plant species. Its genome was sequenced using PacBio's SMRT technology, enabling us to gain insight into the phylogenetic placement of this strain within the genus Xanthomonas, and to study the repertoire of virulence‐associated genes and clusters. Xanthomonas sp. 10‐10 belongs to a clearly defined subclade within clade C (group 2), which includes X. vesicatoria, X. dyei and X. pisi. While this strain is closely related to X. pisi, it represents a new species within the genus Xanthomonas. Surprisingly, this strain lacks a type III secretion system, which is the main virulence determinant in pathogenic Xanthomonas spp., but harbours an arsenal of cell wall‐degrading enzymes. The addition of the organosilicone surfactant Silwet L‐77 drastically increased the disease symptoms caused by Xanthomonas sp. 10‐10 on common ragweed plants grown under controlled conditions, but the plants remained alive. This strain also caused disease symptoms on tomato, pepper and lettuce. More research is needed to develop Xanthomonas‐based bioherbicide specifically targeting common ragweed.