Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders

Abstract Inanimate surfaces that are contaminated with infectious pathogens are common sources of spread for many communicable diseases. Understanding how ambient temperature alters the ability of pathogens to remain viable on these surfaces is critical for understanding how fomites can contribute t...

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Main Authors: Sara R. Teemer, Edan R. Tulman, Alicia G. Arneson, Steven J. Geary, Dana M. Hawley
Format: Article
Language:English
Published: Wiley 2024-12-01
Series:Ecosphere
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Online Access:https://doi.org/10.1002/ecs2.70139
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author Sara R. Teemer
Edan R. Tulman
Alicia G. Arneson
Steven J. Geary
Dana M. Hawley
author_facet Sara R. Teemer
Edan R. Tulman
Alicia G. Arneson
Steven J. Geary
Dana M. Hawley
author_sort Sara R. Teemer
collection DOAJ
description Abstract Inanimate surfaces that are contaminated with infectious pathogens are common sources of spread for many communicable diseases. Understanding how ambient temperature alters the ability of pathogens to remain viable on these surfaces is critical for understanding how fomites can contribute to seasonal patterns of disease outbreaks. House finches (Haemorhous mexicanus) experience fall and winter outbreaks of mycoplasmal conjunctivitis, caused by the bacterial pathogen Mycoplasma gallisepticum (MG). Although bird feeder surfaces serve as an indirect route of MG transmission between sick and healthy individuals, the contributions of feeders to MG transmission in the wild will depend on how ambient temperature affects viability and pathogenicity of MG on feeder surfaces over time. Here, we used two experiments, with identical initial design, to assess such temperature effects. For both experiments, we pipetted equal amounts of MG onto replicate feeder ports held at night‐day temperatures representing summer (22–27°C) or winter (4–9°C). We allowed MG to incubate on feeders at either temperature and swabbed remaining inocula from surfaces at 0, 1, 2, 4, or 7 days post‐inoculation of the feeder, with each replicate feeder port only swabbed at a single time point. In the first study, we analyzed swabs using a culture‐based assay and found that MG incubated at colder versus warmer temperatures maintained higher viability on feeder surfaces over time. In the second study, we replicated the same experimental design but used MG swabs from feeder surfaces to inoculate wild‐caught, pathogen‐naïve birds and measured resulting disease severity and pathogen loads to determine pathogenicity. We found that MG remained pathogenic on feeder surfaces at cold ambient temperatures for up to one week, much longer than previously documented. Further, MG was significantly more pathogenic when incubated on feeders in colder versus warmer temperatures, with the strongest effects of temperature present after at least four days of incubation on feeder surfaces. Overall, cold ambient temperatures appear to alter the role of fomites in the MG transmission process, and temperature likely contributes to seasonal disease dynamics in this system and many others.
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spelling doaj-art-db9606a57f644855b0c3089e061bdaea2025-01-27T14:51:33ZengWileyEcosphere2150-89252024-12-011512n/an/a10.1002/ecs2.70139Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feedersSara R. Teemer0Edan R. Tulman1Alicia G. Arneson2Steven J. Geary3Dana M. Hawley4Department of Biological Sciences Virginia Polytechnic Institute and State University Blacksburg Virginia USADepartment of Pathobiology and Veterinary Science University of Connecticut Storrs Connecticut USADepartment of Biological Sciences Virginia Polytechnic Institute and State University Blacksburg Virginia USADepartment of Pathobiology and Veterinary Science University of Connecticut Storrs Connecticut USADepartment of Biological Sciences Virginia Polytechnic Institute and State University Blacksburg Virginia USAAbstract Inanimate surfaces that are contaminated with infectious pathogens are common sources of spread for many communicable diseases. Understanding how ambient temperature alters the ability of pathogens to remain viable on these surfaces is critical for understanding how fomites can contribute to seasonal patterns of disease outbreaks. House finches (Haemorhous mexicanus) experience fall and winter outbreaks of mycoplasmal conjunctivitis, caused by the bacterial pathogen Mycoplasma gallisepticum (MG). Although bird feeder surfaces serve as an indirect route of MG transmission between sick and healthy individuals, the contributions of feeders to MG transmission in the wild will depend on how ambient temperature affects viability and pathogenicity of MG on feeder surfaces over time. Here, we used two experiments, with identical initial design, to assess such temperature effects. For both experiments, we pipetted equal amounts of MG onto replicate feeder ports held at night‐day temperatures representing summer (22–27°C) or winter (4–9°C). We allowed MG to incubate on feeders at either temperature and swabbed remaining inocula from surfaces at 0, 1, 2, 4, or 7 days post‐inoculation of the feeder, with each replicate feeder port only swabbed at a single time point. In the first study, we analyzed swabs using a culture‐based assay and found that MG incubated at colder versus warmer temperatures maintained higher viability on feeder surfaces over time. In the second study, we replicated the same experimental design but used MG swabs from feeder surfaces to inoculate wild‐caught, pathogen‐naïve birds and measured resulting disease severity and pathogen loads to determine pathogenicity. We found that MG remained pathogenic on feeder surfaces at cold ambient temperatures for up to one week, much longer than previously documented. Further, MG was significantly more pathogenic when incubated on feeders in colder versus warmer temperatures, with the strongest effects of temperature present after at least four days of incubation on feeder surfaces. Overall, cold ambient temperatures appear to alter the role of fomites in the MG transmission process, and temperature likely contributes to seasonal disease dynamics in this system and many others.https://doi.org/10.1002/ecs2.70139ambient temperatureenvironmental persistencefomite transmissionhouse finchesMycoplasma gallisepticumpathogenicity
spellingShingle Sara R. Teemer
Edan R. Tulman
Alicia G. Arneson
Steven J. Geary
Dana M. Hawley
Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders
Ecosphere
ambient temperature
environmental persistence
fomite transmission
house finches
Mycoplasma gallisepticum
pathogenicity
title Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders
title_full Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders
title_fullStr Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders
title_full_unstemmed Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders
title_short Colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders
title_sort colder temperatures augment viability of an indirectly transmitted songbird pathogen on bird feeders
topic ambient temperature
environmental persistence
fomite transmission
house finches
Mycoplasma gallisepticum
pathogenicity
url https://doi.org/10.1002/ecs2.70139
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