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Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii)

Immune function plays an important role in an animal's defense against infectious disease. In reptiles, immune responses may be complex and counterintuitive, and diagnostic tools used to identify infection, such as induced antibody responses are limited. Recent studies using gene transcription...

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Autores principales: Drake, K. Kristina, Aiello, Christina M., Bowen, Lizabeth, Lewison, Rebecca L., Esque, Todd C., Nussear, Kenneth E., Waters, Shannon C., Hudson, Peter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405529/
https://www.ncbi.nlm.nih.gov/pubmed/30891197
http://dx.doi.org/10.1002/ece3.4897
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author Drake, K. Kristina
Aiello, Christina M.
Bowen, Lizabeth
Lewison, Rebecca L.
Esque, Todd C.
Nussear, Kenneth E.
Waters, Shannon C.
Hudson, Peter J.
author_facet Drake, K. Kristina
Aiello, Christina M.
Bowen, Lizabeth
Lewison, Rebecca L.
Esque, Todd C.
Nussear, Kenneth E.
Waters, Shannon C.
Hudson, Peter J.
author_sort Drake, K. Kristina
collection PubMed
description Immune function plays an important role in an animal's defense against infectious disease. In reptiles, immune responses may be complex and counterintuitive, and diagnostic tools used to identify infection, such as induced antibody responses are limited. Recent studies using gene transcription profiling in tortoises have proven useful in identifying immune responses to various intrinsic and extrinsic stressors. As part of a larger experiment with Mojave desert tortoises (Gopherus agassizii), we facilitated the transmission of the pathogenic bacteria, Mycoplasma agassizii (Myag), to naïve adults and measured innate and induced immune reactions over time. Specifically, we evaluated clinical condition, presence of Myag in the nasal/oral cavity, induced antibody responses specific to Myag, and measured molecular reactions (gene transcript profiles) in 15 captive tortoises classified as naïve, exposed, or infected and 14 wild tortoises for comparison. Myag was confirmed inside the nasal/oral cavity in exposed tortoises within 30–60 days of introduction to infected animals, yet we did not detect Myag specific induced antibody responses in these individuals until 420–595 days post exposure. Surprisingly, we found no overall differences in the gene transcript profiles between our experimental treatment groups throughout this study. This work highlights the complexities in assessing immune function and diagnosing pathogen related infections in tortoises and other reptiles.
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spelling pubmed-64055292019-03-19 Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii) Drake, K. Kristina Aiello, Christina M. Bowen, Lizabeth Lewison, Rebecca L. Esque, Todd C. Nussear, Kenneth E. Waters, Shannon C. Hudson, Peter J. Ecol Evol Original Research Immune function plays an important role in an animal's defense against infectious disease. In reptiles, immune responses may be complex and counterintuitive, and diagnostic tools used to identify infection, such as induced antibody responses are limited. Recent studies using gene transcription profiling in tortoises have proven useful in identifying immune responses to various intrinsic and extrinsic stressors. As part of a larger experiment with Mojave desert tortoises (Gopherus agassizii), we facilitated the transmission of the pathogenic bacteria, Mycoplasma agassizii (Myag), to naïve adults and measured innate and induced immune reactions over time. Specifically, we evaluated clinical condition, presence of Myag in the nasal/oral cavity, induced antibody responses specific to Myag, and measured molecular reactions (gene transcript profiles) in 15 captive tortoises classified as naïve, exposed, or infected and 14 wild tortoises for comparison. Myag was confirmed inside the nasal/oral cavity in exposed tortoises within 30–60 days of introduction to infected animals, yet we did not detect Myag specific induced antibody responses in these individuals until 420–595 days post exposure. Surprisingly, we found no overall differences in the gene transcript profiles between our experimental treatment groups throughout this study. This work highlights the complexities in assessing immune function and diagnosing pathogen related infections in tortoises and other reptiles. John Wiley and Sons Inc. 2019-02-18 /pmc/articles/PMC6405529/ /pubmed/30891197 http://dx.doi.org/10.1002/ece3.4897 Text en © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Drake, K. Kristina
Aiello, Christina M.
Bowen, Lizabeth
Lewison, Rebecca L.
Esque, Todd C.
Nussear, Kenneth E.
Waters, Shannon C.
Hudson, Peter J.
Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii)
title Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii)
title_full Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii)
title_fullStr Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii)
title_full_unstemmed Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii)
title_short Complex immune responses and molecular reactions to pathogens and disease in a desert reptile (Gopherus agassizii)
title_sort complex immune responses and molecular reactions to pathogens and disease in a desert reptile (gopherus agassizii)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405529/
https://www.ncbi.nlm.nih.gov/pubmed/30891197
http://dx.doi.org/10.1002/ece3.4897
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