Innate immune function in the diamondback terrapin (Malaclemys terrapin)

The innate immune system serves as a critical first line of defense in reptiles, particularly under the energetic constraints of ectothermy. This study characterizes complement-mediated innate immune responses in the diamondback terrapin ( Malaclemys terrapin ), an estuarine turtle species facing increasing environmental and disease pressures. We evaluated the antibacterial capacity of terrapin plasma against Aeromonas hydrophila , Vibrio vulnificus , Staphylococcus aureus , and Streptococcus pyogenes and assessed complement activity through sheep red blood cell (SRBC) hemolysis assays. Plasma showed strong, concentration-dependent antibacterial activity, with complete inhibition of S. aureus at 100% plasma and substantial inhibition of the other species at ≥25%. Hemolytic activity was rapid, occurring primarily within 10 min, and peaked at 25°C–30°C. Complement activity was abolished by heat, protease, and EDTA treatments and restored with divalent cations, indicating a heat-labile, protease-sensitive mechanism consistent with the alternative complement pathway. Mannan affinity chromatography and SDS-PAGE revealed two major lectins (~25.8 and ~33.4 kDa), consistent with known complement-associated lectins in other emydid turtles. These findings demonstrate that diamondback terrapins possess robust, complement-mediated innate immune responses, potentially shaped by evolutionary exposure to estuarine pathogens like Vibrio spp., and support their use in comparative eco-immunological research and conservation health assessments.

Authors

Institutions

Publication Details

Journal
Frontiers in Amphibian and Reptile Science
Published
2026-02-04
DOI
https://doi.org/10.3389/famrs.2025.1689622
Primary Topic
Turtle Biology and Conservation
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Innate immune function in the diamondback terrapin (Malaclemys terrapin)

Mark Merchant, Sarah J. Baker, Kaylie Delacerda
Frontiers in Amphibian and Reptile Science
Turtle Biology and Conservation
article

Innate immune function in the diamondback terrapin (Malaclemys terrapin)

Mark Merchant, Sarah J. Baker, Kaylie Delacerda
article en

Abstract

The innate immune system serves as a critical first line of defense in reptiles, particularly under the energetic constraints of ectothermy. This study characterizes complement-mediated innate immune responses in the diamondback terrapin ( Malaclemys terrapin ), an estuarine turtle species facing increasing environmental and disease pressures. We evaluated the antibacterial capacity of terrapin plasma against Aeromonas hydrophila , Vibrio vulnificus , Staphylococcus aureus , and Streptococcus pyogenes and assessed complement activity through sheep red blood cell (SRBC) hemolysis assays. Plasma showed strong, concentration-dependent antibacterial activity, with complete inhibition of S. aureus at 100% plasma and substantial inhibition of the other species at ≥25%. Hemolytic activity was rapid, occurring primarily within 10 min, and peaked at 25°C–30°C. Complement activity was abolished by heat, protease, and EDTA treatments and restored with divalent cations, indicating a heat-labile, protease-sensitive mechanism consistent with the alternative complement pathway. Mannan affinity chromatography and SDS-PAGE revealed two major lectins (~25.8 and ~33.4 kDa), consistent with known complement-associated lectins in other emydid turtles. These findings demonstrate that diamondback terrapins possess robust, complement-mediated innate immune responses, potentially shaped by evolutionary exposure to estuarine pathogens like Vibrio spp., and support their use in comparative eco-immunological research and conservation health assessments.

Frontiers in Amphibian and Reptile ScienceVol. 3
McNeese State University (US)
Texas Parks and Wildlife Department
Life below water
Openalex Percentile: Top 77%
Turtle Biology and Conservation
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.