ZFIN ID: ZDB-PUB-150515-4
Immersion infection of germ-free zebrafish with Listeria monocytogenes induces transient expression of innate immune response genes
Shan, Y., Fang, C., Cheng, C., Wang, Y., Peng, J., Fang, W.
Date: 2015
Source: Frontiers in microbiology   6: 373 (Journal)
Registered Authors: Peng, Jinrong
Keywords: Listeria monocytogenes, germ-free zebrafish, immersion, infection model, innate immune responses
MeSH Terms: none
PubMed: 25972853 Full text @ Front Microbiol
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ABSTRACT
Zebrafish, Denio rerio, can be an alternative to other classic animal models for human infectious diseases to examine the processes of microbial infections and host-pathogen interactions in vivo because of their small body dimension but large clutch size. We established germ-free zebrafish infection models of Listeria monocytogenes through different routes of infection: oral immersion and injection via yolk sac, brain ventricle and blood island. Immersion of zebrafish larva even with 10(10) CFU/mL L. monocytogenes EGDe strain in egg water was unable to cause mortality, but GFP-expressing bacteria in the gut lumen can be observed in frozen sections. Several selected maker genes of the innate immune system, including cyp1a, irg1l, il1b, and mmp9, were significantly induced by oral immersion not only with strain EGDe, but also with strain M7 and L. innocua, though to a lesser degree (P < 0.01). Such induction appears to be transient with peak at 48 h post-infection, but returned to basal level at 72 h post-infection. Of the three injection routes, mortality after infection by yolk sac was 80% in early stage of infection. Few eggs can survive and hatch. Injection into zebrafish embryos via brain ventricle or blood island led to progressive lethal infection. L. mocytogenes EGDe showed steady replication in the fish embryos and was far more pathogenic than strain M7, which is consistent with findings in the murine model. We conclude that zebrafish can serve as susceptible and microscopically visible infection models for L. monocytogenes via different routes and can be applied to further studies on the interactions between bacterial virulence factors and host immune responses.
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