Affiliation:
1. Thoracic Diseases Research Unit, Departments of Medicine and Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota 55905
Abstract
ABSTRACT
Pneumocystis
species remain an important cause of life-threatening pneumonia in immunocompromised hosts, including those with AIDS. Responses of the organism to environmental cues both within the lung and elsewhere have been poorly defined. Herein, we report the identification of a cell wall biosynthesis kinase gene (
CBK1
) homologue in
Pneumocystis carinii
, isolated by differential display PCR, that is expressed optimally at physiological pH (7 to 8) as opposed to more acidic environments. Expression of
Pneumocystis CBK1
was also induced by contact with lung epithelial cells and extracellular matrix. Translation of this gene revealed extensive homology to other fungal CBK1 kinases.
Pneumocystis CBK1
expression was equal in the cyst and trophic life forms of the organisms. We further demonstrate that
Pneumocystis CBK1
expressed in
cbk1Δ Saccharomyces cerevisiae
cells restored defective cell wall separation during proliferation. Consistent with this,
Pneumocystis CBK1
expression also stimulated transcription of the
CTS1
chitinase in
cbk1Δ
mutant yeast cells, an event necessary for cell wall separation. In addition,
Pneumocystis CBK1
cDNA supported normal mating projection formation in response to α-factor in the
cbk1Δ
yeast cells. Site-directed mutations of serine-303 and threonine-494, potential regulatory phosphorylation sites in
Pneumocystis
CBK1, abolished mating projection formation, indicating a role for these amino acid residues in CBK1 activity. These findings indicate that
Pneumocystis CBK1
is an environmentally responsive gene that may function in signaling pathways necessary for cell growth and mating.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
28 articles.
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