Malnourished mice develop more severe Norovirus infections and they fail to
mount effective memory immunity to a secondary challenge.
Human noroviruses are the primary cause of severe
childhood diarrhea in the United States, and they are of particular clinical
importance in pediatric populations in the developing world. A major
contributing factor to the general increased severity of infectious diseases in
these regions is malnutrition—nutritional status shapes host immune responses
and the composition of the host intestinal microbiota, both of which can
influence the outcome of pathogenic infections. In terms of enteric norovirus
infections, mucosal immunity and intestinal microbes are likely to contribute
to the infection outcome in substantial ways. We probed these interactions
using a murine model of malnutrition and murine Norovirus infection. Our results reveal that malnutrition is associated
with more severe Norovirus infections
as defined by weight loss, impaired control of norovirus infections, reduced
antiviral antibody responses, loss of protective immunity, and enhanced viral
evolution. Moreover, the microbiota is dramatically altered by malnutrition.
Interestingly, murine norovirus infection also causes changes in the host
microbial composition within the intestine but only in healthy mice. In fact,
the infection-associated microbiota resembles the malnutrition-associated microbiota.
Collectively, these findings represent an extensive characterization of a new
malnutrition model of norovirus infection that will ultimately facilitate
elucidation of the nutritionally regulated host parameters that predispose to
more severe infections and impaired memory immune responses. In a broad sense,
this model may provide insight into the reduced efficacy of oral vaccines in
malnourished hosts and the potential for malnourished individuals to act as
reservoirs of emergent virus strains.
Malnourished children in developing countries are
susceptible to more severe infections than their healthy counterparts, in
particular enteric infections that cause diarrhea. In order to probe the
effects of malnutrition on an enteric infection in a well-controlled system
devoid of other environmental and genetic variability, we studied Norovirus infection in a mouse model. We
have revealed that malnourished mice develop more severe norovirus infections
and they fail to mount effective memory immunity to a secondary challenge. This
is of particular importance because malnourished children generally mount less
effective immune responses to oral vaccines, and we can now use our new model
system to probe the immunological basis of this impairment. We have also
determined that noroviruses evolve more readily in the face of malnutrition.
Finally, both Norovirus infection and malnutrition independently alter the
composition of the intestinal microbiota in substantial and overlapping ways.
Source: mBio
5(2):e01032-13. doi:10.1128/mBio.01032-13.
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