Affiliation:
1. Department of Ecology and Evolutionary Biology University of Connecticut Storrs Connecticut USA
2. Institute for Systems Genomics, University of Connecticut Storrs Connecticut USA
3. Department of Science and Technology University of Maryland College Park Maryland USA
4. School of Earth and Environment University of Canterbury Christchurch New Zealand
5. Department of Biological Sciences Northern Illinois University DeKalb Illinois USA
6. Department of Biology San Francisco State University San Francisco California USA
7. Colegio de Ciencias Biológicas y Ambientales Universidad San Francisco de Quito Quito Ecuador
Abstract
AbstractHuman activity changes multiple factors in the environment, which can have positive or negative synergistic effects on organisms. However, few studies have explored the causal effects of multiple anthropogenic factors, such as urbanization and invasive species, on animals and the mechanisms that mediate these interactions. This study examines the influence of urbanization on the detrimental effect of invasive avian vampire flies (Philornis downsi) on endemic Darwin's finches in the Galápagos Islands. We experimentally manipulated nest fly abundance in urban and non‐urban locations and then characterized nestling health, fledging success, diet, and gene expression patterns related to host defense. Fledging success of non‐parasitized nestlings from urban (79%) and non‐urban (75%) nests did not differ significantly. However, parasitized, non‐urban nestlings lost more blood, and fewer nestlings survived (8%) compared to urban nestlings (50%). Stable isotopic values (δ15N) from urban nestling feces were higher than those from non‐urban nestlings, suggesting that urban nestlings are consuming more protein. δ15N values correlated negatively with parasite abundance, which suggests that diet might influence host defenses (e.g., tolerance and resistance). Parasitized, urban nestlings differentially expressed genes within pathways associated with red blood cell production (tolerance) and pro‐inflammatory response (innate immunological resistance), compared to parasitized, non‐urban nestlings. In contrast, parasitized non‐urban nestlings differentially expressed genes within pathways associated with immunoglobulin production (adaptive immunological resistance). Our results suggest that urban nestlings are investing more in pro‐inflammatory responses to resist parasites but also recovering more blood cells to tolerate blood loss. Although non‐urban nestlings are mounting an adaptive immune response, it is likely a last effort by the immune system rather than an effective defense against avian vampire flies since few nestlings survived.
Funder
National Science Foundation
University of Connecticut
National Geographic Society
Subject
General Environmental Science,Ecology,Environmental Chemistry,Global and Planetary Change