Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae)

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae). / Fernández-Marín, Hermógenes; Bruner, Gaspar; Gomez, Ernesto B.; Nash, David Richard; Boomsma, Jacobus Jan; Wcislo, William T.

In: American Naturalist, Vol. 181, No. 4, 2013, p. 571-582.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Fernández-Marín, H, Bruner, G, Gomez, EB, Nash, DR, Boomsma, JJ & Wcislo, WT 2013, 'Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae)', American Naturalist, vol. 181, no. 4, pp. 571-582. https://doi.org/10.1086/669664

APA

Fernández-Marín, H., Bruner, G., Gomez, E. B., Nash, D. R., Boomsma, J. J., & Wcislo, W. T. (2013). Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae). American Naturalist, 181(4), 571-582. https://doi.org/10.1086/669664

Vancouver

Fernández-Marín H, Bruner G, Gomez EB, Nash DR, Boomsma JJ, Wcislo WT. Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae). American Naturalist. 2013;181(4):571-582. https://doi.org/10.1086/669664

Author

Fernández-Marín, Hermógenes ; Bruner, Gaspar ; Gomez, Ernesto B. ; Nash, David Richard ; Boomsma, Jacobus Jan ; Wcislo, William T. / Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae). In: American Naturalist. 2013 ; Vol. 181, No. 4. pp. 571-582.

Bibtex

@article{c128caa9d0e44b25b596905bea7157fd,
title = "Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae)",
abstract = "Abstract Multipartner mutualisms have potentially complex dynamics, with compensatory responses when one partner is lost or relegated to a minor role. Fungus-growing ants (Attini) are mutualistic associates of basidiomycete fungi and antibiotic-producing actinomycete bacteria; the former are attacked by specialized fungi (Escovopsis) and diverse generalist microbes. Ants deploy biochemical defenses from bacteria and metapleural glands (MGs) and express different behaviors to control contaminants. We studied four Trachymyrmex species that differed in relative abundance of actinomycetes to understand interactions among antimicrobial tactics that are contingent on the nature of infection. MG grooming rate and actinomycete abundance were negatively correlated. The two species with high MG grooming rates or abundant actinomycetes made relatively little use of behavioral defenses. Conversely, the two species with relatively modest biochemical defenses relied heavily on behavior. Trade-offs suggest that related species can evolutionarily diverge to rely on different defense mechanisms against the same threat. Neither bacterial symbionts nor MG secretions thus appear to be essential for mounting defenses against the specialized pathogen Escovopsis, but reduced investment in one of these defense modes tends to increase investment in the other.",
author = "Herm{\'o}genes Fern{\'a}ndez-Mar{\'i}n and Gaspar Bruner and Gomez, {Ernesto B.} and Nash, {David Richard} and Boomsma, {Jacobus Jan} and Wcislo, {William T.}",
year = "2013",
doi = "10.1086/669664",
language = "English",
volume = "181",
pages = "571--582",
journal = "American Naturalist",
issn = "0003-0147",
publisher = "University of Chicago Press",
number = "4",

}

RIS

TY - JOUR

T1 - Dynamic disease management in trachymyrmex fungus-growing ants (Attini: Formicidae)

AU - Fernández-Marín, Hermógenes

AU - Bruner, Gaspar

AU - Gomez, Ernesto B.

AU - Nash, David Richard

AU - Boomsma, Jacobus Jan

AU - Wcislo, William T.

PY - 2013

Y1 - 2013

N2 - Abstract Multipartner mutualisms have potentially complex dynamics, with compensatory responses when one partner is lost or relegated to a minor role. Fungus-growing ants (Attini) are mutualistic associates of basidiomycete fungi and antibiotic-producing actinomycete bacteria; the former are attacked by specialized fungi (Escovopsis) and diverse generalist microbes. Ants deploy biochemical defenses from bacteria and metapleural glands (MGs) and express different behaviors to control contaminants. We studied four Trachymyrmex species that differed in relative abundance of actinomycetes to understand interactions among antimicrobial tactics that are contingent on the nature of infection. MG grooming rate and actinomycete abundance were negatively correlated. The two species with high MG grooming rates or abundant actinomycetes made relatively little use of behavioral defenses. Conversely, the two species with relatively modest biochemical defenses relied heavily on behavior. Trade-offs suggest that related species can evolutionarily diverge to rely on different defense mechanisms against the same threat. Neither bacterial symbionts nor MG secretions thus appear to be essential for mounting defenses against the specialized pathogen Escovopsis, but reduced investment in one of these defense modes tends to increase investment in the other.

AB - Abstract Multipartner mutualisms have potentially complex dynamics, with compensatory responses when one partner is lost or relegated to a minor role. Fungus-growing ants (Attini) are mutualistic associates of basidiomycete fungi and antibiotic-producing actinomycete bacteria; the former are attacked by specialized fungi (Escovopsis) and diverse generalist microbes. Ants deploy biochemical defenses from bacteria and metapleural glands (MGs) and express different behaviors to control contaminants. We studied four Trachymyrmex species that differed in relative abundance of actinomycetes to understand interactions among antimicrobial tactics that are contingent on the nature of infection. MG grooming rate and actinomycete abundance were negatively correlated. The two species with high MG grooming rates or abundant actinomycetes made relatively little use of behavioral defenses. Conversely, the two species with relatively modest biochemical defenses relied heavily on behavior. Trade-offs suggest that related species can evolutionarily diverge to rely on different defense mechanisms against the same threat. Neither bacterial symbionts nor MG secretions thus appear to be essential for mounting defenses against the specialized pathogen Escovopsis, but reduced investment in one of these defense modes tends to increase investment in the other.

U2 - 10.1086/669664

DO - 10.1086/669664

M3 - Journal article

C2 - 23535621

VL - 181

SP - 571

EP - 582

JO - American Naturalist

JF - American Naturalist

SN - 0003-0147

IS - 4

ER -

ID: 44980390