secreted bacterial effectors and host-produced eigertnf drive death in a salmonella-infected fruit fly分泌细菌效果器和host-produced eigertnf开车在受感染的果蝇死亡.pdfVIP
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secreted bacterial effectors and host-produced eigertnf drive death in a salmonella-infected fruit fly分泌细菌效果器和host-produced eigertnf开车在受感染的果蝇死亡
Open access, freely available online PLoS BIOLOGY
Secreted Bacterial Effectors
and Host-Produced Eiger/TNF Drive Death
in a Salmonella-Infected Fruit Fly
*
Stephanie M. Brandt, Marc S. Dionne, Ranjiv S. Khush, Linh N. Pham, Thomas J. Vigdal, David S. Schneider
Department of Microbiology and Immunology, Stanford University, Stanford, California, United States of America
Death by infection is often as much due to the host’s reaction as it is to the direct result of microbial action. Here we
identify genes in both the host and microbe that are involved in the pathogenesis of infection and disease in
Drosophila melanogaster challenged with Salmonella enterica serovar typhimurium (S. typhimurium). We demonstrate
that wild-type S. typhimurium causes a lethal systemic infection when injected into the hemocoel of D. melanogaster.
Deletion of the gene encoding the secreted bacterial effector Salmonella leucine-rich (PslrP) changes an acute and
lethal infection to one that is persistent and less deadly. We propose a model in which Salmonella secreted effectors
stimulate the fly and thus cause an immune response that is damaging both to the bacteria and, subsequently, to the
host. In support of this model, we show that mutations in the fly gene eiger, a TNF homolog, delay the lethality of
Salmonella infection. These results suggest that S. typhimurium-infected flies die from a condition that resembles TNF-
induced metabolic collapse in vertebrates. This idea provides us with a new model to study shock-like biology in a
genetically manipulable host. In addition, it allows us to study the difference in pathways followed by a microbe when
producing an acute or persiste
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