Xylella fastidiosa
(
Xf
) bacteria form biofilm on the cuticular surfaces of the functional foregut (precibarium and cibarium) of its vectors, xylem fluid-ingesting sharpshooter leafhoppers and spittlebugs. While much is known about
Xf
biofilm development and maturation
in vitro
, little is known about these processes in vectors. Real-time (RT)-PCR was used to quantify
Xf
genomes daily in the functional foreguts of blue-green sharpshooters,
Graphocephala atropunctata,
over 7 days of exposure to infected grapevines. Scanning electron microscopy (SEM) was used to examine
Xf
biofilm formation at 4 and 7 days of that time course. PCR showed populations building and reducing over a 4-day cycle. SEM revealed that foreguts at 4 days showed variability in quantity and location of bacterial attachment. Only early-stage biofilm formation occurred in low-turbulence areas of the cibarium, while high-turbulence areas of the cibarium and precibarium had rare but older, more developed macro-colonies. Biofilm was almost absent at 7 days but left behind adhesive material and remnants of prior colonization. Evidence supports the hypothesis that bacterial colonization was repeatedly interrupted and constrained by the vector. Behaviors such as egestion and enzymatic salivation likely can loosen and eject
Xf
biofilm, perhaps when profuse biofilm interferes with ingestion. Thus, vector acquisition of
Xf
is a dynamic and stochastic process of interactions between bacteria and insects. We further hypothesize for future testing that the insect can regulate this interaction. A deep understanding of
Xf
acquisition will aid the ongoing development of grapevine resistance to vector transmission of xylellae diseases.
IMPORTANCE
Xylella fastidiosa
(
Xf
) is one of the most destructive invasive plant pathogens in the world, able to hijack new vectors when it invades a region; yet the temporal interplay of bacterial colonization and insect behavior is unknown. This paper describes important findings about the process of
Xf
biofilm formation and maturation in a vector, contrasting similarities and differences with such formation
in vitro
. Results support the hypothesis that the behavior of the vector constrains and may regulate
Xf
biofilm formation, in dynamic competition with the bacterium. The data from this paper partly explain why
Xf
is so successful at invasion. Because the bacterium can be acquired and inoculated very quickly, it can move readily from old to new vectors and host plants in all-new environments. Our findings are relevant to biosecurity decisions because they demonstrate the importance of identifying potential vector species in the
Xylella
invasion front.