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British Journal of Experimental Pathology logoLink to British Journal of Experimental Pathology
. 1980 Aug;61(4):415–420.

Histopathological changes in the lungs of influenza-infected mice superinfected with Staphylococcus aureus.

I D Gardner, T M Kung
PMCID: PMC2041600  PMID: 6252936

Abstract

Histopathological changes in the lung were assessed in a model infection of mice using swine influenza virus and Staphylococcus aureus. Virus preinfection markedly enhanced both the persistence of S. aureus and the extent and duration of the inflammatory response. Lymphocytic infiltration was increased and regeneration and squamous metaplasia were delayed, suggesting an enhancement of an immunopathological response to the virus. Mice with the dual infection showed a decrease in phagocytic cell infiltration of the lung compared to that observed in those with the bacterial infection only, and this may reflect a decline in alveolar macrophage function after influenza infection.

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Selected References

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  1. Cambridge G., Mackenzie J. S., Keast D. Cell-mediated immune response to influenza virus infections in mice. Infect Immun. 1976 Jan;13(1):36–43. doi: 10.1128/iai.13.1.36-43.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cate T. R., Mold N. G. Increased influenza pneumonia mortality of mice adoptively immunized with node and spleen cells sensitized by inactivated but not live virus. Infect Immun. 1975 May;11(5):908–914. doi: 10.1128/iai.11.5.908-914.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Degré M., Glasgow L. A. Synergistic effect in viral-bacterial infection. I. Combined infection of the respiratory tract in mice with parainfluenza virus and Hemophilus influenza. J Infect Dis. 1968 Dec;118(5):449–462. doi: 10.1093/infdis/118.5.449. [DOI] [PubMed] [Google Scholar]
  4. Degré M., Solberg L. A. Synergistic effect in viral-bacterial infection. 3. Histopathological changes in the trachea of mice following viral and bacterial infection. Acta Pathol Microbiol Scand B Microbiol Immunol. 1971;79(2):129–136. [PubMed] [Google Scholar]
  5. Eyckmans L., Billiau A. Inhibition of bactericidal capacity in mice after administration of Newcastle disease virus. Scand J Infect Dis. 1972;4(2):101–104. doi: 10.3109/inf.1972.4.issue-2.06. [DOI] [PubMed] [Google Scholar]
  6. GERONE P. J., WARD T. G., CHAPPELL W. A. Combined infections in mice with influenza virus and Diplococcus pneumoniae. Am J Hyg. 1957 Nov;66(3):331–341. doi: 10.1093/oxfordjournals.aje.a119906. [DOI] [PubMed] [Google Scholar]
  7. GREEN G. M., KASS E. H. THE ROLE OF THE ALVEOLAR MACROPHAGE IN THE CLEARANCE OF BACTERIA FROM THE LUNG. J Exp Med. 1964 Jan 1;119:167–176. doi: 10.1084/jem.119.1.167. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Greenberg S. B., Criswell B. S., Six H. R., Couch R. B. Lymphocyte cytotoxicity to influenza virus-infected cells: response to vaccination and virus infection. Infect Immun. 1978 Jun;20(3):640–645. doi: 10.1128/iai.20.3.640-645.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hamilton J. R., Overall J. C., Glasgow L. A. Synergistic effect on mortality in mice with murine cytomegalovirus and Pseudomonas aeruginosa, Staphylococcus aureus, or Candida albicans infections. Infect Immun. 1976 Oct;14(4):982–989. doi: 10.1128/iai.14.4.982-989.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hugh R., Huang K. Y., Elliott T. B. Enhancement of bacterial infections in mice by newcastle disease virus. Infect Immun. 1971 Mar;3(3):488–493. doi: 10.1128/iai.3.3.488-493.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Jakab G. J., Warr G. A., Knight M. E. Pulmonary and systemic defenses against challenge with Staphylococcus aureus in mice with pneumonia due to influenza A virus. J Infect Dis. 1979 Jul;140(1):105–108. doi: 10.1093/infdis/140.1.105. [DOI] [PubMed] [Google Scholar]
  12. Kleinerman E. S., Snyderman R., Daniels C. A. Depressed monocyte chemotaxis during acute influenza infection. Lancet. 1975 Nov 29;2(7944):1063–1066. doi: 10.1016/s0140-6736(75)90432-8. [DOI] [PubMed] [Google Scholar]
  13. Kleinerman E. S., Snyderman R., Daniels C. A. Depression of human monocyte chemotaxis by herpes simplex and influenza viruses. J Immunol. 1974 Nov;113(5):1562–1567. [PubMed] [Google Scholar]
  14. LOURIA D. B., BLUMENFELD H. L., ELLIS J. T., KILBOURNE E. D., ROGERS D. E. Studies on influenza in the pandemic of 1957-1958. II. Pulmonary complications of influenza. J Clin Invest. 1959 Jan;38(1 Pt 2):213–265. doi: 10.1172/JCI103791. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Larson H. E., Blades R. Impairment of human polymorphonuclear leucocyte function by influenza virus. Lancet. 1976 Feb 7;1(7954):283–283. doi: 10.1016/s0140-6736(76)91407-0. [DOI] [PubMed] [Google Scholar]
  16. Loosli C. G. Influenza and the interaction of viruses and bacteria in respiratory infections. Medicine (Baltimore) 1973 Sep;52(5):369–384. doi: 10.1097/00005792-197309000-00001. [DOI] [PubMed] [Google Scholar]
  17. McMichael A. J., Askonas B. A. Influenza virus-specific cytotoxic T cells in man; induction and properties of the cytotoxic cell. Eur J Immunol. 1978 Oct;8(10):705–711. doi: 10.1002/eji.1830081007. [DOI] [PubMed] [Google Scholar]
  18. Ruutu P., Vaheri A., Kosunen T. U. Depression of human neutrophil motility by influenza virus in vitro. Scand J Immunol. 1977;6(9):897–906. doi: 10.1111/j.1365-3083.1977.tb00410.x. [DOI] [PubMed] [Google Scholar]
  19. SELLERS T. F., Jr, SCHULMAN J., BOUVIER C., McCUNE R., KILBOURNE E. D. The influence of influenza virus infection on exogenous staphylococcal and endogenous murine bacterial infection of the bronchopulmonary tissues of mice. J Exp Med. 1961 Aug 1;114:237–256. doi: 10.1084/jem.114.2.237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Shayegani M., Lief F. S., Mudd S. Specific and nonspecific cell-mediated resistance to influenza virus in mice. Infect Immun. 1974 Jun;9(6):991–998. doi: 10.1128/iai.9.6.991-998.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Warshauer D., Goldstein E., Akers T., Lippert W., Kim M. Effect of influenza viral infection on the ingestion and killing of bacteria by alveolar macrophages. Am Rev Respir Dis. 1977 Feb;115(2):269–277. doi: 10.1164/arrd.1977.115.2.269. [DOI] [PubMed] [Google Scholar]
  22. Yap K. L., Ada G. L. Cytotoxic T cells in the lungs of mice infected with an influenza A virus. Scand J Immunol. 1978;7(1):73–80. doi: 10.1111/j.1365-3083.1978.tb00428.x. [DOI] [PubMed] [Google Scholar]
  23. Yap K. L., Ada G. L. Cytotoxic T cells specific for influenza virus-infected target cells. Immunology. 1977 Feb;32(2):151–159. [PMC free article] [PubMed] [Google Scholar]
  24. Yealland S. J., Heath R. B. The significance of secondary gram-negative coliform infection of the lungs of mice with influenzal pneumonitis. Br J Exp Pathol. 1978 Feb;59(1):48–51. [PMC free article] [PubMed] [Google Scholar]

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