Gf. Jones et al., COMPARISON OF TECHNIQUES FOR DIAGNOSIS OF PROLIFERATIVE ENTERITIS OF SWINE, American journal of veterinary research, 54(12), 1993, pp. 1980-1985
In an abattoir-based case-control study, histologic, and macroscopic e
xamination of porcine intestines at slaughter and 2 molecular assays w
ere compared for use as diagnostic tests of proliferative enteritis (P
E). Fecal samples and intestinal specimens were collected from pigs wi
th grossly thick ileum and from clinically normal pigs at slaughter. T
issue specimens were fixed in neutral buffered 10% formalin, and secti
oned. Sections stained with H&E were examined for proliferative lesion
s by a pathologist unaware of the group to which the pig had been assi
gned on the basis of results of gross examination. Adjacent tissue sec
tions, stained with Warthin-Starry (silver) stain, were examined for p
resence of the intracellular bacterium of PE, ileal symbiont (IS)-intr
acellularis, in the enterocytes of the intestinal crypts by the senior
author, who was unaware either of the group to which the pig had been
assigned or diagnosis by the pathologist. Bacterial DNA was extracted
from the fecal samples and assayed by dot-blot hybridization and poly
merase chain reaction (PCR) for presence of IS-intracellularis DNA, wi
thout knowledge of results of the other examinations. The PCR assay fo
r IS-intracellularis was a specific and sensitive diagnostic test for
PE, and dot-blot hybridization was sensitive, but was less specific. M
acroscopic examination of intestines at slaughter was a sensitive, but
not specific, test. Association between IS-intracellularis and prolif
erative lesions was statistically examined in the same study. There wa
s a highly significant (P = 0.0078) association between presence of na
turally acquired proliferative lesions and intracellular infection by
IS-intracellularis, The odds ratio of greater than or equal to 14 and
estimated attributable fraction of greater than or equal to 32% indica
te that IS-intracellularis may be a necessary cause of PE.