Skip to main content
Proceedings of the Royal Society B: Biological Sciences logoLink to Proceedings of the Royal Society B: Biological Sciences
. 2001 Jan 22;268(1463):207–211. doi: 10.1098/rspb.2000.1352

The effects of testosterone on a viral infection in greenfinches (Carduelis chloris): an experimental test of the immunocompetence-handicap hypothesis.

K M Lindström 1, D Krakower 1, J O Lundström 1, B Silverin 1
PMCID: PMC1088593  PMID: 11209893

Abstract

The immunocompetence-handicap hypothesis suggests that the honesty of quality signals could be guaranteed if testosterone (T) suppresses immune function while enhancing male ornaments. In addition, it has been proposed that the cost of enhancing ornaments should be highest for males with small ornaments. Recently, the assertion that T causes obligate immunosuppression has been questioned. In this study, we tested whether elevated T levels would increase susceptibility to a viral infection, and whether this hypothesized effect would be most pronounced in males with small ornaments. We surgically inserted T implants into 15 male greenfinches (Carduelis chloris) and control implants into a further 15 males. All birds were then infected with a naturally occurring virus (Sindbis virus, Alphavirus genus), and each bird's daily viraemia (blood virus concentration) was measured for seven days. The specific antibody response was measured for eight weeks. T-implanted males did not exhibit increased viraemia or decreased antibody response, and males with small and large ornaments did not respond differently to T implantation. We did, however, find that T implantation decreased viraemia early in the course of the infection and increased viraemia late in the infection. Thus, our results demonstrate that T may act both to increase and to decrease viraemia.

Full Text

The Full Text of this article is available as a PDF (124.8 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Deviche P., Wingfield J. C., Sharp P. J. Year-class differences in the reproductive system, plasma prolactin and corticosterone concentrations, and onset of prebasic molt in male dark-eyed juncos (Junco hyemalis) during the breeding period. Gen Comp Endocrinol. 2000 Jun;118(3):425–435. doi: 10.1006/gcen.2000.7478. [DOI] [PubMed] [Google Scholar]
  2. Earley E., Peralta P. H., Johnson K. M. A plaque neutralization method for arboviruses. Proc Soc Exp Biol Med. 1967 Jul;125(3):741–747. doi: 10.3181/00379727-125-32194. [DOI] [PubMed] [Google Scholar]
  3. Francy D. B., Jaenson T. G., Lundström J. O., Schildt E. B., Espmark A., Henriksson B., Niklasson B. Ecologic studies of mosquitoes and birds as hosts of Ockelbo virus in Sweden and isolation of Inkoo and Batai viruses from mosquitoes. Am J Trop Med Hyg. 1989 Sep;41(3):355–363. [PubMed] [Google Scholar]
  4. Grafen A. Biological signals as handicaps. J Theor Biol. 1990 Jun 21;144(4):517–546. doi: 10.1016/s0022-5193(05)80088-8. [DOI] [PubMed] [Google Scholar]
  5. Grossman C. J. Interactions between the gonadal steroids and the immune system. Science. 1985 Jan 18;227(4684):257–261. doi: 10.1126/science.3871252. [DOI] [PubMed] [Google Scholar]
  6. Lundström J. O. Mosquito-borne viruses in western Europe: a review. J Vector Ecol. 1999 Jun;24(1):1–39. [PubMed] [Google Scholar]
  7. Lundström J. O., Niklasson B., Francy D. B. Swedish Culex torrentium and Cx. pipiens (Diptera: Culicidae) as experimental vectors of Ockelbo virus. J Med Entomol. 1990 Jul;27(4):561–563. doi: 10.1093/jmedent/27.4.561. [DOI] [PubMed] [Google Scholar]
  8. Møller A. P., Christe P., Lux E. Parasitism, host immune function, and sexual selection. Q Rev Biol. 1999 Mar;74(1):3–20. doi: 10.1086/392949. [DOI] [PubMed] [Google Scholar]
  9. Norder H., Lundström J. O., Kozuch O., Magnius L. O. Genetic relatedness of Sindbis virus strains from Europe, Middle East, and Africa. Virology. 1996 Aug 15;222(2):440–445. doi: 10.1006/viro.1996.0441. [DOI] [PubMed] [Google Scholar]
  10. Olsen N. J., Kovacs W. J. Gonadal steroids and immunity. Endocr Rev. 1996 Aug;17(4):369–384. doi: 10.1210/edrv-17-4-369. [DOI] [PubMed] [Google Scholar]
  11. Olson K., Trent D. W. Genetic and antigenic variations among geographical isolates of Sindbis virus. J Gen Virol. 1985 Apr;66(Pt 4):797–810. doi: 10.1099/0022-1317-66-4-797. [DOI] [PubMed] [Google Scholar]
  12. Peters A. Testosterone treatment is immunosuppressive in superb fairy-wrens, yet free-living males with high testosterone are more immunocompetent. Proc Biol Sci. 2000 May 7;267(1446):883–889. doi: 10.1098/rspb.2000.1085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Zahavi A. Mate selection-a selection for a handicap. J Theor Biol. 1975 Sep;53(1):205–214. doi: 10.1016/0022-5193(75)90111-3. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings. Biological sciences / The Royal Society are provided here courtesy of The Royal Society

RESOURCES