TY - JOUR
T1 - Functionally distinct T-helper cell phenotypes predict resistance to different types of parasites in a wild mammal
AU - Corripio-Miyar, Yolanda
AU - Hayward, Adam
AU - Lemon, Hannah
AU - Sweeny, Amy R.
AU - Bal, Xavier
AU - Kenyon, Fiona
AU - Pilkington, Jill G.
AU - Pemberton, Josephine M.
AU - Nussey, Daniel H.
AU - McNeilly, Tom N.
N1 - Funding Information:
This work was funded by a large NERC Grant (NE/R016801/1) and the long-term study on St Kilda was funded principally by responsive mode grants from NERC. We thank the National Trust for Scotland for their ongoing support of our work on St Kilda, and QinetiQ and Kilda Cruises for logistical support. We are very grateful to the 2019 August St Kilda Soay sheep project catch team, without whom the samples we used in this study could not have been collected.
Funding Information:
This work was funded by a large NERC Grant (NE/R016801/1) and the long-term study on St Kilda was funded principally by responsive mode grants from NERC. We thank the National Trust for Scotland for their ongoing support of our work on St Kilda, and QinetiQ and Kilda Cruises for logistical support. We are very grateful to the 2019 August St Kilda Soay sheep project catch team, without whom the samples we used in this study could not have been collected.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/2/24
Y1 - 2022/2/24
N2 - The adaptive immune system is critical to an effective response to infection in vertebrates, with T-helper (Th) cells pivotal in orchestrating these responses. In natural populations where co-infections are the norm, different Th responses are likely to play an important role in maintaining host health and fitness, a relationship which remains poorly understood in wild animals. In this study, we characterised variation in functionally distinct Th responses in a wild population of Soay sheep by enumerating cells expressing Th-subset specific transcription factors and quantifying Th-associated cytokines. We tested the prediction that raised Th1 and Th2 responses should predict reduced apicomplexan and helminth parasite burdens, respectively. All measures of Th-associated cytokine production increased with age, while Th17- and regulatory Th-associated cytokine production increased more rapidly with age in males than females. Independent of age, sex, and each other, IL-4 and Gata3 negatively predicted gastro-intestinal nematode faecal egg count, while IFN-γ negatively predicted coccidian faecal oocyst count. Our results provide important support from outside the laboratory that Th1 and Th2 responses predict resistance to different kinds of parasites, and illustrate how harnessing specific reagents and tools from laboratory immunology will illuminate our understanding of host-parasite interactions in the wild.
AB - The adaptive immune system is critical to an effective response to infection in vertebrates, with T-helper (Th) cells pivotal in orchestrating these responses. In natural populations where co-infections are the norm, different Th responses are likely to play an important role in maintaining host health and fitness, a relationship which remains poorly understood in wild animals. In this study, we characterised variation in functionally distinct Th responses in a wild population of Soay sheep by enumerating cells expressing Th-subset specific transcription factors and quantifying Th-associated cytokines. We tested the prediction that raised Th1 and Th2 responses should predict reduced apicomplexan and helminth parasite burdens, respectively. All measures of Th-associated cytokine production increased with age, while Th17- and regulatory Th-associated cytokine production increased more rapidly with age in males than females. Independent of age, sex, and each other, IL-4 and Gata3 negatively predicted gastro-intestinal nematode faecal egg count, while IFN-γ negatively predicted coccidian faecal oocyst count. Our results provide important support from outside the laboratory that Th1 and Th2 responses predict resistance to different kinds of parasites, and illustrate how harnessing specific reagents and tools from laboratory immunology will illuminate our understanding of host-parasite interactions in the wild.
U2 - 10.1038/s41598-022-07149-9
DO - 10.1038/s41598-022-07149-9
M3 - Article
SN - 2045-2322
VL - 12
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 3197
ER -