Quantification and assessment of viability of Pneumocystis carinii organisms by flow cytometry

Author:

Lapinsky S E1,Glencross D1,Car N G1,Kallenbach J M1,Zwi S1

Affiliation:

1. Division of Pulmonology, University of the Witwatersrand Medical School, Parktown, Johannesburg, South Africa.

Abstract

Analysis of drug efficacy in animal models of Pneumocystis carinii pneumonia requires an accurate method of quantification of organisms, as well as a means of assessing viability. Lung homogenates were prepared from a colony of athymic nude F344 rats experiencing a spontaneous outbreak of P. carinii pneumonia. With the fluorescent nucleic acid stain propidium iodide, flow cytometric analysis was able to quantify P. carinii cysts and trophozoites reproducibly. As this stain is excluded by living cells, this method was also used to assess the viability of organisms. Application of this technique to analysis of bronchoalveolar lavage specimens was demonstrated.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference18 articles.

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3. In vitro differentiation of human-derived Pneumocystis carinii;Blumenfeld W.;J. Clin. Microbiol.,1989

4. Isolation of mononuclear cells and granulocytes from human blood;Boyum A.;Scand. J. Clin. Lab. Invest.,1968

5. Diagnosis of Pneumocystis carinii in sputum samples using a modified toluidine blue 0 method;Cohen R. J.;Acta Cytol.,1990

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