Wolbachia are cytoplasmically inherited bacteria that cause a number of rep
roductive alterations in insects, including cytoplasmic incompatibility(1,2
), an incompatibility between sperm and egg that results in loss of sperm c
hromosomes following fertilization. Wolbachia are estimated to infect 15-20
% of all insect species(3), and also are common in arachnids, isopods and n
ematodes(3,4). Therefore, Wolbachia-induced cytoplasmic incompatibility cou
ld be an important factor promoting rapid speciation in invertebrates(5), a
lthough this contention is controversial(6,7). Here we show that high level
s of bidirectional cytoplasmic incompatibility between two closely related
species of insects (the parasitic wasps Nasonia giraulti and Nasonia longic
ornis) preceded the evolution of other postmating reproductive barriers. Th
e presence of Wolbachia severely reduces the frequency of hybrid offspring
in interspecies crosses. However, antibiotic curing of the insects results
in production of hybrids. Furthermore, F-1 and F-2 hybrids are completely v
iable and fertile, indicating the absence of F-1 and F-2 hybrid breakdown.
Partial interspecific sexual isolation occurs, yet it is asymmetric and inc
omplete. Our results indicate that Wolbachia-induced reproductive isolation
occurred in the early stages of speciation in this system, before the evol
ution of other postmating isolating mechanisms (for example, hybrid inviabi
lity and hybrid sterility).