Pneumocystis carinii pneumonia (PCP) is a leading cause of death among
AIDS patients in the United States. Our analysis of P. carinii protei
n-coding genes has revealed a significant A + T codon bias. Polymerase
chain reaction (PCR) was utilized to isolate and identify the genes e
ncoding calmodulin, beta-tubulin, DNA polymerase II, and RNA polymeras
es I, II and III from P. carinii. Primer pairs were designed to incorp
orate P. carinii codon preference to known conserved protein regions f
rom other organisms. This strategy should be useful for a large variet
y of P. carinii genes and assist in the comprehensive analysis of the
genomic structure of this important pathogen.