An early-life disruption of gut microbiota has opposing effects on
parasite resistance in two host species
Abstract
The gut microbiome regulates multiple aspects of host health, including
metabolism and the development of the immune system. Despite this, we
still know relatively little about how the gut microbiome influences
host responses to parasitism in wild organisms, particularly whether
interactions between gut microbiota and host physiology contribute to
variation in parasitism across host species. The goal of this study was
to determine the role of gut microbiota in shaping how birds respond to
nest parasites and investigate whether this relationship varies between
host species. Both eastern bluebirds (Sialia sialis) and tree swallows
(Tachycineta bicolor) are parasitized by blow flies (Protocalliphora
sialia) which produce larvae that feed on nestlings’ blood. We
experimentally manipulated the gut microbiota of nestling bluebirds and
tree swallows by dosing nestlings with an oral antibiotic or sterile
water as a control. We then quantified nestling physiology (hemoglobin,
glucose, parasite specific IgY antibodies), body morphometrics, and
survival until fledging, as well as nest parasite abundance and size. We
found that an experimental disruption of nestling gut microbiota
increased parasite abundance in tree swallows, but decreased parasite
abundance in bluebirds. Treatment with antibiotics was associated with
delayed parasite development, including reduced pupation volume of
parasites found as larvae in bluebird nests. Similarly, antibiotic
treatment was associated with larger size differences in pupal volume
between parasites found as larvae and pupae in swallow nests. Both
antibiotic treatment and parasite abundance had variable effects on
nestling body morphometrics and physiology across the two host species.
Together, these results suggest that gut microbiota contribute to host
differences in resistance to P. sialia and can influence host-parasite
interactions.