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Infect Immun, August 1998, p. 3941-3951, Vol. 66, No. 8
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Phospholipase A of Yersinia
enterocolitica Contributes to Pathogenesis in a Mouse
Model
D. H.
Schmiel,1 2
E.
Wagar,3
L.
Karamanou,1
D.
Weeks,1 and
V. L.
Miller1 2 4 5 *
Department of Microbiology and Molecular
Genetics1 and the
Molecular Biology
Institute,4 University of California, and
Department of Pathology and Laboratory Medicine, University of
California at Los Angeles School of Medicine,3
Los Angeles, California 90095; and
Department of Molecular
Microbiology2 and
Department of
Pediatrics,5 Washington University School of
Medicine, St. Louis, Missouri 63110
Received 20 March 1998/Returned for modification 22 April
1998/Accepted 11 May 1998
Some isolates of Yersinia enterocolitica exhibit
phospholipase activity, which has been linked to lecithin-dependent
hemolysis (M. Tsubokura, K. Otsoki, I. Shimohira, and H. Yamamoto,
Infect. Immun. 25:939-942, 1979). A gene encoding Y. enterocolitica phospholipase was identified, and analysis of the
nucleotide sequence revealed two tandemly transcribed open reading
frames. The first, yplA, has 74% identity and 85%
similarity to the phospholipase A found in Serratia
liquefaciens. Though the other, yplB, was less
similar to the downstream accessory protein found in S. liquefaciens, the organization in both species is similar.
Subsequently, a yplA-null Y. enterocolitica
strain, YEDS10, was constructed and demonstrated to be phospholipase
negative by plate and spectrophotometric assays. To ascertain whether
the phospholipase has a role in pathogenesis, YEDS10 was tested in the
mouse model. In experiments with perorally infected BALB/c mice, fewer
YEDS10 organisms were recovered from the mesenteric lymph nodes and
Peyer's patches (PP) than the parental strain at 3 or 5 days
postinfection. Furthermore, bowel tissue and PP infected with YEDS10
appeared to be less inflamed than those infected with the parental
strain. When extremely high doses of both the parental and YEDS10
strains were given, similar numbers of viable bacteria were recovered
from the PP and mesenteric lymph nodes on day 3. However, the numbers
of foci and the extent of inflammation and necrosis within them were
noticeably less for YEDS10 compared to the parental strain. Together
these findings suggest that Y. enterocolitica produces a
phospholipase A which has a role in pathogenesis.
*
Corresponding author. Mailing address: Department of
Molecular Microbiology, Washington University School of Medicine,
Campus Box 8230, 660 S. Euclid Ave., St. Louis, MO 63110-1093. Phone: (314) 747-2132. Fax: (314) 747-2135. E-mail:
virginia{at}borcim.wustl.edu.
Infect Immun, August 1998, p. 3941-3951, Vol. 66, No. 8
0019-9567/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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