N. Dorrell et al., Whole genome comparison of Campylobacter jejuni human isolates using a low-cost microarray reveals extensive genetic diversity, GENOME RES, 11(10), 2001, pp. 1706-1715
Campylobacter jejuni is the leading cause of bacterial food-borne diarrhoea
l disease throughout the world, and yet is still a poorly understood pathog
en. Whole genome microarray comparisons of 11 C jefuni strains of diverse o
rigin identified genes in up to 30 NCTC 11168 loci ranging from 0.7 to 18.7
kb that are either absent or highly divergent in these isolates. Many of t
hese regions are associated with the biosynthesis of surface structures inc
luding flagella, lipo-oligosaccharide, and the newly identified capsule. Ot
her strain-variable genes of known function include those responsible for i
ron acquisition, DNA restriction/modification, and sialylation. In fact, at
least 21% of genes in the sequenced strain appear dispensable as they are
absent or highly divergent in one or more of the isolates tested, thus defi
ning 1300 C jejuni core genes. Such core genes contribute mainly to metabol
ic, biosynthetic, cellular, and regulatory processes, but many virulence de
terminants are also conserved. Comparison of the capsule biosynthesis locus
revealed conservation of all the genes in this region in strains with the
same Penner serotype as strain NCTC 11168. By contrast, between 5 and 17 NC
TC 11168 genes in this region are either absent or highly divergent in stra
ins of a different serotype from the sequenced strain, providing further ev
idence that the capsule accounts for Penner serotype specificity. These stu
dies reveal extensive genetic diversity among C jejuni strains and pave the
way toward identifying correlates of pathogenicity and developing improved
epidemiological tools for this problematic pathogen.