Affiliation:
1. Division of Comparative Medicine, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Bldg. 16-825, Cambridge, Massachusetts 02139
2. Department of Molecular Genetics, The Forsyth Institute, Boston, Massachusetts 02115
Abstract
ABSTRACT
We recently described helicobacter-associated progressive, proliferative, and dysplastic typhlocolitis in aging (18- to 24-month-old) Syrian hamsters. Other pathogens associated with typhlocolitis in hamsters,
Clostridium difficile
,
Lawsonia intracellularis
, and
Giardia
spp., were not indentified. The presence of
Helicobacter
genus-specific DNA was noted by PCR in cecal and paraffin-embedded liver samples from aged hamsters by the use of
Helicobacter
-specific PCR primers. By 16S rRNA analysis, the
Helicobacter
sp. isolated from the liver tissue was identical to the cecal isolates from hamsters. The six hamster 16S rRNA sequences form a genotypic cluster most closely related to
Helicobacter
sp.
Flexispira
taxon 8, part of the
Helicobacter bilis
/
H. cinaedi
group. Livers from aged helicobacter-infected hamsters showed various stages of predominantly portocentric and, to a lesser extent, perivenular fibrosis. Within nodules, there was cellular atypia consistent with nodular dysplasia. The livers also exhibited a range of chronic active portal/interface and lobular inflammation, with significant portal hepatitis being present. The inflammation was composed of a mixture of lymphocytes, neutrophils, and macrophages, indicative of its chronic-active nature in these aged hamsters infected with
Helicobacter
spp. The isolation of novel
Helicobacter
spp., their identification by PCR from the diseased livers of aged hamsters, and their taxonomic classification as belonging to the
Helicobacter bilis
cluster strengthen the argument that
H. bilis
and closely related
Helicobacter
spp. play an etiological role in hepatobiliary disease in both animals and humans.
Publisher
American Society for Microbiology
Cited by
36 articles.
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