Host-specificity and recognition by root-infecting pathogens are revie
wed, with emphasis on fungi but drawing parallels with other root para
sites, symbionts and rhizosphere micro-organisms. Two major levels of
specificity are identified: family-specific parasitism, exemplified by
many parasites that characteristically infect Gramineae, and the poss
ibly recent segregation of pathogen species into crop-specific strains
. In both of these cases there are examples where host-specificity is
paralleled by host-recognition in the pre-infection stages, including
host-specific triggering of propagule germination. The pre-infection s
equence of zoosporic pathogens (Pythium, Phytophthora, Aphanomyces spp
.) is reviewed. These fungi seem to have both general (low-affinity) a
nd host-specific (high-affinity) receptor-based recognition systems fo
r chemotaxis to root diffusates and for induction of encystment by hos
t surface components. Zoospores orientate (dock) during encystment, an
d the cysts germinate from a fixed point, whereas the non-motile spore
s of at least some root parasites (e.g. Idriella bolleyi) can germinat
e from any point, which is influenced by the host.The possession of bo
th general and host-specific recognition systems by a parasite could e
nable it to exploit rhizosphere niches or to invade compromised plants
in the absence of preferred hosts. Evidence from graminicolous (famil
y-specific) Pythium spp. suggests that host-specific recognition is qu
antitative rather than absolute but, when compounded over successive c
ycles of infection, is a powerful selective mechanism.