Affiliation:
1. Zentralinstitut für Ernährungs und Lebensmittelforschung, Abteilung Biochemie
2. Abteilung Mikrobiologie, Technische Universität München, 85350 Freising, Germany
3. Lehrstuhl für Mikrobielle Ökologie, Department für biowissenschaftliche Grundlagen, Wissenschaftszentrum Weihenstephan, Technische Universität München, 85350 Freising, Germany
Abstract
ABSTRACT
Caenorhabditis elegans
is a validated model to study bacterial pathogenicity. We report that
Yersinia enterocolitica
strains W22703 (biovar 2, serovar O:9) and WA314 (biovar 1B, serovar O:8) kill
C. elegans
when feeding on the pathogens for at least 15 min before transfer to the feeding strain
Escherichia coli
OP50. The killing by
Yersinia enterocolitica
requires viable bacteria and, in contrast to that by
Yersinia pestis
and
Yersinia pseudotuberculosis
strains, is biofilm independent. The deletion of
tcaA
encoding an insecticidal toxin resulted in an OP50-like life span of
C. elegans
, indicating an essential role of TcaA in the nematocidal activity of
Y. enterocolitica
. TcaA alone is not sufficient for nematocidal activity because
E. coli
DH5α overexpressing TcaA did not result in a reduced
C. elegans
life span. Spatial-temporal analysis of
C. elegans
infected with green fluorescent protein-labeled
Y. enterocolitica
strains showed that
Y. enterocolitica
colonizes the nematode intestine, leading to an extreme expansion of the intestinal lumen. By low-dose infection with W22703 or DH5α followed by transfer to
E. coli
OP50, proliferation of
Y. enterocolitica
, but not
E. coli
, in the intestinal lumen of the nematode was observed. The titer of W22703 cells within the worm increased to over 10
6
per worm 4 days after infection while a significantly lower number of a
tcaA
knockout mutant was recovered. A strong expression of
tcaA
was observed during the first 5 days of infection.
Y. enterocolitica
WA314 (biovar 1B, serovar O:8) mutant strains lacking the
yadA
,
inv
,
yopE
, and
irp1
genes known to be important for virulence in mammals were not attenuated or only slightly attenuated in their toxicity toward the nematode, suggesting that these factors do not play a significant role in the colonization and persistence of this pathogen in nematodes. In summary, this study supports the hypothesis that
C. elegans
is a natural host and nutrient source of
Y. enterocolitica
.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Reference55 articles.
1. Aballay, A., E. Drenkard, L. R. Hilbun, and F. M. Ausubel. 2003. Caenorhabditis elegans innate immune response triggered by Salmonella enterica requires intact LPS and is mediated by a MAPK signaling pathway. Curr. Biol.13:47-52.
2. Aballay, A., P. Yorgey, and F. M. Ausubel. 2000. Salmonella typhimurium proliferates and establishes a persistent infection in the intestine of Caenorhabditis elegans. Curr. Biol.10:1539-1542.
3. Aleksic, S., J. Bockemuhl, and H. H. Wuthe. 1995. Epidemiology of Y. pseudotuberculosis in Germany, 1983-1993. Contrib. Microbiol. Immunol.13:55-58.
4. Hydrogen Peroxide-Mediated Killing of
Caenorhabditis elegans
: a Common Feature of Different Streptococcal Species
5. Bottone, E. J. 1999. Yersinia enterocolitica: overview and epidemiologic correlates. Microbes Infect.1:323-333.
Cited by
31 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献