Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1983 Jul;41(1):275-9.
doi: 10.1128/iai.41.1.275-279.1983.

Experimental pneumococcal meningitis: role of leukocytes in pathogenesis

Experimental pneumococcal meningitis: role of leukocytes in pathogenesis

J D Ernst et al. Infect Immun. 1983 Jul.

Abstract

Two groups of rabbits with experimental meningitis induced by direct intracisternal inoculation of Streptococcus pneumoniae cells were studied. One group was rendered profoundly leukopenic by nitrogen mustard, and the other had normal leukocyte counts. The two groups had comparable bacterial growth rates (mean generation time, 60 versus 67 min) and ultimate bacterial populations in the cerebrospinal fluid (CSF) (mean log10 CFU, 9.1 versus 8.7); therefore leukocytes did not effectively slow or limit the growth of pneumococci in the CSF in vivo. Increased CSF protein, decreased CSF glucose, and increased CSF lactate levels were similar in both groups, suggesting that leukocytes are not essential for these changes to occur. Quantitative blood cultures revealed identical levels of pneumococcal bacteremia until 13 to 14 h after the initiation of infection, when the leukopenic rabbits showed a larger number of pneumococci in the blood, ultimately exceeding the number reached in nonleukopenic rabbits by 100-fold. Leukocytes therefore limit the extent of pneumococcal bacteremia after infection of the CSF despite their lack of effect on the course or the CSF manifestations of experimental meningitis.

PubMed Disclaimer

References

    1. J Infect Dis. 1975 Oct;132(4):355-60 - PubMed
    1. J Lab Clin Med. 1978 Jun;91(6):979-88 - PubMed
    1. J Lab Clin Med. 1980 Mar;95(3):362-72 - PubMed
    1. J Clin Invest. 1980 Aug;66(2):243-53 - PubMed
    1. J Infect Dis. 1980 Dec;142(6):903-9 - PubMed

LinkOut - more resources