Abstract
Intravenous injection of pregnant mice with St. Louis encephalitis (SLE) virus at 8 days of gestation resulted in infection of the fetus. Progeny developed no antibody or tolerance to SLE virus since the viral antigen was cleared by maternal antibody before antibody-forming competence developed in the young. Temporary growth retardation was observed in a number of young at 3 weeks of age. After the initial setback the growth rate increased, indicating that early runting was due to an inability to adjust adequately to extrauterine life, which was subsequently overcome. In most other young there were no significant effects on growth, reproduction, or life expectancy. A few young died at or shortly after birth; in these, neurological changes ranging from gross defects such as encephaloceles and hydrocephalus to histological evidence of necrosis and congestion were observed. Neurologically related behavioral changes were detected by using the open field test and the rotating-rod test, which indicated neurological damage and memory impairment in the surviving intrauterinely infected animals.
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- Andersen A. A., Hanson R. P. Experimental transplacental transmission of st. Louis encephalitis virus in mice. Infect Immun. 1970 Sep;2(3):320–325. doi: 10.1128/iai.2.3.320-325.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BURNS K. F. Congenital Japanese B encephalitis infection of swine. Proc Soc Exp Biol Med. 1950 Nov;75(2):621–625. doi: 10.3181/00379727-75-18285. [DOI] [PubMed] [Google Scholar]
- Hotcin J., Sikora E. Long-term effects of virus infection on behavior and aging in mice. Proc Soc Exp Biol Med. 1970 May;134(1):204–209. doi: 10.3181/00379727-134-34760. [DOI] [PubMed] [Google Scholar]
- Kilham L., Margolis G. Pathogenesis of intrauterine infections in rats due to reovirus type 3. I. Virologic studies. Lab Invest. 1973 May;28(5):597–604. [PubMed] [Google Scholar]
- RANZENHOFER E. R., ALEXANDER E. R., BEADLE L. D., BERNSTEIN A., PICKARD R. C. St. Louis encephalitis in Calvert City, Kentucky, 1955; an epidemiologic study. Am J Hyg. 1957 Mar;65(2):147–161. doi: 10.1093/oxfordjournals.aje.a119862. [DOI] [PubMed] [Google Scholar]
- SHIMIZU T., KAWAKAMI Y., FUKUHARA S., MATUMOTO M. Experimental stillbirth in pregnant swine infected with Japanese encephalitis virus. Jpn J Exp Med. 1954 Dec;24(6):363–375. [PubMed] [Google Scholar]
- SHINEFIELD H. R., TOWNSEND T. E. Transplacental transmission of western equine encephalomyelitis. J Pediatr. 1953 Jul;43(1):21–25. doi: 10.1016/s0022-3476(53)80082-x. [DOI] [PubMed] [Google Scholar]
- St Geme J. W., Jr, Peralta H., Van Pelt L. F. Intrauterine infection of the rhesus monkey with mumps virus: abbreviated viral replication in the immature fetus as an explanation for split immunologic recognition after birth. J Infect Dis. 1972 Sep;126(3):249–256. doi: 10.1093/infdis/126.3.249. [DOI] [PubMed] [Google Scholar]
- Swanson H. H. Interaction of experience with adrenal and sex hormones on the behaviour of hamsters in the open field test. Anim Behav. 1969 Feb;17(1):148–154. doi: 10.1016/0003-3472(69)90123-7. [DOI] [PubMed] [Google Scholar]
- TRIPOD J., BEIN H. J., MEIER R. Characterization of central effects of serpasil (reserpin, a new alkaloid of Rauwolfia serpentina B.) and of their antagonistic reactions. Arch Int Pharmacodyn Ther. 1954 Jan;96(3-4):406–425. [PubMed] [Google Scholar]
- Whimbey A. E., Denenberg V. H. Two independent behavioral dimensions in open-field performance. J Comp Physiol Psychol. 1967 Jun;63(3):500–504. doi: 10.1037/h0024620. [DOI] [PubMed] [Google Scholar]