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. 1984 Apr;50(1):66–72. doi: 10.1128/jvi.50.1.66-72.1984

Pathogenesis of in utero infections with abortogenic and non-abortogenic alphaviruses in mice.

A R Milner, I D Marshall
PMCID: PMC255583  PMID: 6321801

Abstract

The initial stages of infection of pregnant mice at gestation day 11 with either the T48 strain of Ross River virus or avirulent Semliki Forest virus are similar. With both infections, a hematogenous spread of virus to the placenta occurs. The viruses subsequently replicate to high titer in all placentas and are able to persist in the presence of specific maternal antiviral antibodies. There is a delay of at least 1 to 2 days between the initial detection of virus in the placenta and the onset of fetal infection. With Semliki Forest virus, abortion occurred in all mothers and appeared to be preceded by infection of all fetuses. However, when Semliki Forest virus was given at other stages of pregnancy, abortion was less common, and in all non-aborted pregnancies at least one uninfected fetus was observed. This situation was similar to that with Ross River virus, in which abortion was not observed and fetal infection and death were only seen in a proportion of fetuses. Within each pregnancy, the outcome of the two in utero infections appeared to result from similar mechanisms, with the fate of an individual fetus depending upon the timing of the passive transfer of anti-viral immunoglobulin G from the mother relative to the timing of fetal infection by virus from the placenta. Although the passive maternal immunoglobulin G protected susceptible fetuses against infection, antibody did not mediate in utero recovery of infected fetuses or clear placental infection.

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Selected References

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

  1. ALFORD C. A., Jr, NEVA F. A., WELLER T. H. VIROLOGIC AND SEROLOGIC STUDIES ON HUMAN PRODUCTS OF CONCEPTION AFTER MATERNAL RUBELLA. N Engl J Med. 1964 Dec 17;271:1275–1281. doi: 10.1056/NEJM196412172712501. [DOI] [PubMed] [Google Scholar]
  2. Aaskov J. G., Davies C. E., Tucker M., Dalglish D. Effect on mice of infection during pregnancy with three Australian arboviruses. Am J Trop Med Hyg. 1981 Jan;30(1):198–203. doi: 10.4269/ajtmh.1981.30.198. [DOI] [PubMed] [Google Scholar]
  3. Atkins G. J., Carter J., Sheahan B. J. Effect of alphavirus infection on mouse embryos. Infect Immun. 1982 Dec;38(3):1285–1290. doi: 10.1128/iai.38.3.1285-1290.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bell S. C., Billington W. D. Major anti-paternal alloantibody induced by murine pregnancy is non-complement-fixing IgG1. Nature. 1980 Nov 27;288(5789):387–388. doi: 10.1038/288387a0. [DOI] [PubMed] [Google Scholar]
  5. Brenière S., Viens P. Trypanosoma musculi: transfer of immunity from mother mice to litter. Can J Microbiol. 1980 Sep;26(9):1090–1095. doi: 10.1139/m80-181. [DOI] [PubMed] [Google Scholar]
  6. CLARKE D. H., CASALS J. Techniques for hemagglutination and hemagglutination-inhibition with arthropod-borne viruses. Am J Trop Med Hyg. 1958 Sep;7(5):561–573. doi: 10.4269/ajtmh.1958.7.561. [DOI] [PubMed] [Google Scholar]
  7. Carretti N., Ovary Z. Transmission of gamma G antibodies from maternal to fetal circulation in the mouse. Proc Soc Exp Biol Med. 1969 Feb;130(2):509–512. doi: 10.3181/00379727-130-33592. [DOI] [PubMed] [Google Scholar]
  8. Ey P. L., Prowse S. J., Jenkin C. R. Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-sepharose. Immunochemistry. 1978 Jul;15(7):429–436. doi: 10.1016/0161-5890(78)90070-6. [DOI] [PubMed] [Google Scholar]
  9. FAHEY J. L., BARTH W. F. THE IMMUNOGLOBULINS OF MICE. 4. SERUM IMMUNOGLOBULIN CHANGES FOLLOWING BIRTH. Proc Soc Exp Biol Med. 1965 Mar;118:596–600. doi: 10.3181/00379727-118-29914. [DOI] [PubMed] [Google Scholar]
  10. Grey H. M., Hirst J. W., Cohn M. A new mouse immunoglobulin: IgG3. J Exp Med. 1971 Feb 1;133(2):289–304. doi: 10.1084/jem.133.2.289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hapel A. J. The protective role of thymus-derived lymphocytes in arbovirus-induced meningoencephalitis. Scand J Immunol. 1975;4(3):267–278. doi: 10.1111/j.1365-3083.1975.tb02626.x. [DOI] [PubMed] [Google Scholar]
  12. Hayes K., Gibas H. Placental cytomegalovirus infection without fetal involvement following primary infection in pregnancy. J Pediatr. 1971 Sep;79(3):401–405. doi: 10.1016/s0022-3476(71)80147-6. [DOI] [PubMed] [Google Scholar]
  13. Johnson K. P. Mouse cytomegalovirus: placental infection. J Infect Dis. 1969 Oct;120(4):445–450. doi: 10.1093/infdis/120.4.445. [DOI] [PubMed] [Google Scholar]
  14. Kendrick J. W., Schneider L., Straub O. C. Placental reaction to the infectious bovine rhinotracheitis-infectious pustular vulvovaginitis virus. Am J Vet Res. 1971 Jul;32(7):1045–1051. [PubMed] [Google Scholar]
  15. Kilham L., Margolis G., Colby E. D. Congenital infections of cats and ferrets by feline panleukopenia virus manifested by cerebellar hypoplasia. Lab Invest. 1967 Nov;17(5):465–480. [PubMed] [Google Scholar]
  16. Milner A. R., Marshall I. D., Mullbacher A. Effect of pregnancy on stimulation of alphavirus immunity in mice. J Virol. 1984 Apr;50(1):73–76. doi: 10.1128/jvi.50.1.73-76.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Mims C. A. Pathogenesis of viral infections of the fetus. Prog Med Virol. 1968;10:194–237. [PubMed] [Google Scholar]
  18. Osburn B. I., Johnson R. T., Silverstein A. M., Prendergast R. A., Jochim M. M., Levy S. E. Experimental viral-induced congenital encephalopathies. II. The pathogenesis of bluetongue vaccine virus infection in fetal lambs. Lab Invest. 1971 Sep;25(3):206–210. [PubMed] [Google Scholar]
  19. Osburn B. I., Silverstein A. M., Prendergast R. A., Johnson R. T., Parshall C. J., Jr Experimental viral-induced congenital encephalopathies. I. Pathology of hydranencephaly and porencephaly caused by bluetongue vaccine virus. Lab Invest. 1971 Sep;25(3):197–205. [PubMed] [Google Scholar]
  20. Parsonson I. M., Della-Porta A. J., Snowdon W. A. Congenital abnormalities in newborn lambs after infection of pregnant sheep with Akabane virus. Infect Immun. 1977 Jan;15(1):254–262. doi: 10.1128/iai.15.1.254-262.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Rylatt D. B., Parish C. R. Protein determination on an automatic spectrophotometer. Anal Biochem. 1982 Mar 15;121(1):213–214. doi: 10.1016/0003-2697(82)90578-4. [DOI] [PubMed] [Google Scholar]
  22. SEVER J. L. Application of a microtechnique to viral serological investigations. J Immunol. 1962 Mar;88:320–329. [PubMed] [Google Scholar]
  23. Seppälä I., Sarvas H., Péterfy F., Mäkelä O. The four subclasses of IgG can be isolated from mouse serum by using Protein A-Sepharose. Scand J Immunol. 1981 Oct;14(4):335–342. doi: 10.1111/j.1365-3083.1981.tb00573.x. [DOI] [PubMed] [Google Scholar]
  24. Siiteri P. K., Stites D. P. Immunologic and endocrine interrelationships in pregnancy. Biol Reprod. 1982 Feb;26(1):1–14. doi: 10.1095/biolreprod26.1.1. [DOI] [PubMed] [Google Scholar]
  25. Tachibana D. K., Rosenberg L. T. Fetal synthesis of Hc', a component of mouse complement. J Immunol. 1966 Aug;97(2):213–215. [PubMed] [Google Scholar]
  26. Tikasingh E. S., Spence L., Downs W. G. The use of adjuvant and sarcoma 180 cells in the production of mouse hyperimmune ascitic fluids to arboviruses. Am J Trop Med Hyg. 1966 Mar;15(2):219–226. doi: 10.4269/ajtmh.1966.15.219. [DOI] [PubMed] [Google Scholar]

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