Jg. Fox et al., LOCAL IMMUNE-RESPONSE IN HELICOBACTER PYLORI-INFECTED CATS AND IDENTIFICATION OF HELICOBACTER-PYLORI IN SALIVA, GASTRIC FLUID AND FECES, Immunology, 88(3), 1996, pp. 400-406
Helicobacter pylori-infected cats were screened by culture and polymer
ase chain reaction (PCR) for the presence of H. pylori in salivary sec
retions, gastric juice, gastric tissue and faeces. H. pylori was cultu
red from salivary secretions in six of 12 (50%) cats and from gastric
fluid samples in 11 of 12 (91%) cats. A 298 base pair polymerase chain
reactions (PCR) product specific for an H. pylori 26 000 MW surface p
rotein was amplified from dental plaque samples from five of 12 (42%)
cats and from the faeces of four of five (80%) cats studied. Analyses
of serum and mucosal secretions by enzyme-linked immunosorbent assay (
ELISA) revealed an H. pylori-specific immunoglobulin G (IgG) response,
and elevated IgA anti-H. pylori antibody levels in salivary and local
gastric secretions. Immunohistochemical analyses of gastric tissue re
vealed the presence of IgM(+) B cells assembled into multiple lymphoid
follicles surrounded by clusters of CD4(+) and CD8(+) T cells. The la
mina propria also contained single cells or aggregates of IgA(+) and I
gM(+) B cells. These observations show that H. pylori can be identifie
d in feline mucosal secretions, and that a localized IgA immune respon
se develops in gastric tissue of H. pylori-infected cats. The findings
suggest a zoonotic risk from exposure to personnel handling H. pylori
-infected cats in vivaria.