The mechanism by which the neonicotinoid pesticide clothianidin (CLO) disrupts the intestinal microbiota of experimental animals is unknown. We focused on α-defensins, which are regulators
of the intestinal microbiota. Subchronic exposure to CLO induced dysbiosis and reduced short-chain fatty acid–producing bacteria in the intestinal microbiota of mice. Levels of cryptdin-1
(Crp1, a major α-defensin in mice) in feces and cecal contents were lower in the CLO-exposed groups than in control. In Crp1 immunostaining, Paneth cells in the jejunum and ileum of the
no-observed-adverse-effect-level CLO-exposed group showed a stronger positive signal than control, likely due to the suppression of Crp1 release. Our results showed that CLO exposure
suppresses α-defensin secretion from Paneth cells as part of the mechanism underlying CLO-induced dysbiosis.