Relationship between phylogeny and immunity suggests older Caribbean coral lineages are more resistant to disease

PLoS One. 2014 Aug 18;9(8):e104787. doi: 10.1371/journal.pone.0104787. eCollection 2014.

Abstract

Diseases affect coral species fitness and contribute significantly to the deterioration of coral reefs. The increase in frequency and severity of disease outbreaks has made evaluating and determining coral resistance a priority. Phylogenetic patterns in immunity and disease can provide important insight to how corals may respond to current and future environmental and/or biologically induced diseases. The purpose of this study was to determine if immunity, number of diseases and disease prevalence show a phylogenetic signal among Caribbean corals. We characterized the constitutive levels of six distinct innate immune traits in 14 Caribbean coral species and tested for the presence of a phylogenetic signal on each trait. Results indicate that constitutive levels of some individual immune related processes (i.e. melanin concentration, peroxidase and inhibition of bacterial growth), as well as their combination show a phylogenetic signal. Additionally, both the number of diseases affecting each species and disease prevalence (as measures of disease burden) show a significant phylogenetic signal. The phylogenetic signal of immune related processes, combined with estimates of species divergence times, indicates that among the studied species, those belonging to older lineages tend to resist/fight infections better than more recently diverged coral lineages. This result, combined with the increasing stressful conditions on corals in the Caribbean, suggest that future reefs in the region will likely be dominated by older lineages while modern species may face local population declines and/or geographic extinction.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Anthozoa / genetics
  • Anthozoa / immunology*
  • Disease Resistance / genetics*
  • Genetic Speciation
  • Immunity, Innate
  • Phylogeny
  • Puerto Rico
  • RNA, Ribosomal, 28S / genetics
  • Sequence Analysis, DNA

Substances

  • RNA, Ribosomal, 28S

Grants and funding

Funding was provided by NSF grant IOS # 1017458 to L.D.M., NSF grant IOS # 1017510 and OCE -1105143 to E.W., and NSF grant OCE-PRF # 1225163 to J.H.P.C. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.