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axenic-gnotobiotic model, we show that anterior midgut alkalinization necessitates colonization by "live" bacteria belonging to selected genera. Results of our bacteriophage-mediated gut bacteria decolonization studies suggest that the colonizing bacteria also mediate the expression of crucial larval proteases. Additionally, the colonizing bacteria contribute a significant proportion of proteases (including serine proteases, aminopeptidases, etc.) to the larval gut, which are crucial for the digestion of dietary proteins. Collectively, these findings reveal that specific members of the gut microbiota promote larval growth and development by facilitating larval protein metabolism through modulation of the midgut microenvironment. These findings may have important implications for the development of targeted vector-control strategies.
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Samanta et al. (2025) studied this question.
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