We have shown previously that type IV pili (TFP) are required for wild-type levels of virulence of A. citrulli on melon and that this pathogen can colonize and move thorough the xylem vessels of host seedlings.

Here, comparative studies between wild-type and TFP mutant strains using microfluidic flow chambers demonstrated that TFP play a critical role in both the surface attachment and the biofilm formation of A. citrulli under a medium flow. Additionally, TFP null mutants were unable to perform twitching movement against the direction of medium Paclitaxel concentration flow. Assays using a flagellin mutant showed that, in contrast to TFP, polar flagella do not contribute to the adhesion and biofilm formation of A. citrulli under tested conditions. Also, flagellum-mediated swimming motility of wild-type strains was not observed under medium flow. These results imply that TFP may play an important role in colonization and spread in the xylem vessels under sap flow conditions, while polar flagella could be more important for spread during periods of time when xylem flow is minimal. Acidovorax avenae ssp. citrulli (Schaad et al., 1978; Willems et al., 1992) is a Gram-negative bacterium

that causes bacterial fruit blotch (BFB) of cucurbit plants. The destructive potential of this bacterium was fully realized during the late 1980s, following severe BFB outbreaks in watermelon fields in the United States that led to high yield

check details losses of up to 100% (Latin & Hopkins, 1995; Schaad et al., 2003). Since then, the Atazanavir disease has spread to different parts of the world, causing severe yield losses in watermelon and melon (Bahar & Burdman, 2010). Recently, Schaad et al. (2008) suggested a new classification for subspecies of A. avenae, with A. avenae ssp. citrulli being reclassified as Acidovorax citrulli. Herein, we adopt this new nomenclature. Molecular, biochemical and host-range characterization of A. citrulli isolates revealed the existence of two distinct groups: group I includes strains isolated mainly from nonwatermelon plants, while group II includes strains isolated mostly from watermelon (Walcott et al., 2000, 2004; Burdman et al., 2005; Feng et al., 2009). The genome of a group II strain (AAC00-1) has been sequenced recently by the Joint Genome Institute. Few studies have shed light on the transmission mechanisms of A. citrulli inside the plant. It has been shown that this bacterium can penetrate the plant through blossoms and subsequently infect seeds (Walcott et al., 2003; Lessl et al., 2007). In a recent study, we showed that A. citrulli can systemically infect melon seedlings and can move basipetally and acropetally through the xylem vessels (Bahar et al., 2009). The aforementioned studies suggest that motility contributes to both infection and translocation of the bacterium throughout the plant.