Expression and complexity of the PRT1 multigene family of Pneumocystis carinii

被引:23
作者
Ambrose, HE
Keely, SP
Aliouat, EM
Dei-Cas, E
Wakefield, AE
Miller, RF
Stringer, JR [1 ]
机构
[1] Univ Cincinnati, Dept Mol Genet Biochem & Microbiol, Cincinnati, OH 45267 USA
[2] Inst Pasteur, F-59019 Lille, France
[3] Fac Pharm, Dept Parasitol, F-59006 Lille, France
[4] Lille 2 Univ Hosp, Lille, France
[5] Univ Oxford, Weatherall Inst Mol Med, Mol Infect Dis Grp, Oxford OX3 9DU, England
[6] UCL, Royal Free & Univ Coll Med Sch, Dept Sexually Transmitted Dis, London WC1 6AU, England
来源
MICROBIOLOGY-SGM | 2004年 / 150卷
关键词
D O I
10.1099/mic.0.26539-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Pneumocystis carinii has a multigene family, PRT1, that encodes proteins with homology to KEX2-like proteases. PRT1 genes cluster with MSG genes near the telomeres and, like MSG, PRT1 proteins seem to be surface-expressed. The clustering of PRT1 and MSG genes suggested that expression of the two multigene families might be coordinated. Studying gene expression in P. carinii has been hampered by the lack of a culture system, and by lack of clonality in P. carinii populations in naturally infected rats, the host of this fungus. Heterogeneity can be reduced, however, by low-dose intratracheal inoculation, which can produce P. carinii populations dominated by organisms derived from a single progenitor. To study PRT1 expression, nude rats were inoculated with approximately 10 P. carinii each. The clonality of the P. carinii populations from inoculated rats was assessed by analysis of the UCS locus, a site in the genome that is known to be very heterogeneous in naturally infected rats, but nearly homogeneous in rats infected by low-dose intratracheal inoculation. Each of the populations had the same MSG gene at the UCS locus in at least 80% of the organisms. To investigate PRT1 gene expression, RNA was amplified using primers that amplify numerous PRT1 genes. Seventy-four cloned cDNAs were sequenced, including at least 12 clones from each population of P. carinii. Many differently expressed PRT1 sequences were identified in each population, and a total of 45 different sequences were detected. However, the same PRT1 sequence was present in 15 of 74 plasmids and was found in 3 of the 5 P. carinii populations, suggesting that some PRT1 genes may be either more commonly expressed or expressed at a higher level. These data show that many members of the PRT1 gene family can be expressed in populations of P. carinii derived from few progenitors and suggest that the regulation of this family is different from that governing expression of the MSG gene family.
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页码:293 / 300
页数:8
相关论文
共 45 条
[1]   PNEUMOCYSTIS-CARINII ORGANISMS FROM IN-VITRO CULTURE ARE HIGHLY INFECTIOUS TO THE NUDE RAT [J].
ALIOUAT, EM ;
DEICAS, E ;
BILLAUT, P ;
DUJARDIN, L ;
CAMUS, D .
PARASITOLOGY RESEARCH, 1995, 81 (01) :82-85
[2]   In vitro pharmacodynamic parameters of sordarin derivatives in comparison with those of marketed compounds against Pneumocystis carinii isolated from rats [J].
Aviles, P ;
Aliouat, EM ;
Martinez, A ;
Dei-Cas, E ;
Herreros, E ;
Dujardin, L ;
Gargallo-Viola, D .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (05) :1284-1290
[3]   VARIABLE ANTIGEN GENES OF THE RELAPSING FEVER AGENT BORRELIA-HERMSII ARE ACTIVATED BY PROMOTER ADDITION [J].
BARBOUR, AG ;
BURMAN, N ;
CARTER, CJ ;
KITTEN, T ;
BERGSTROM, S .
MOLECULAR MICROBIOLOGY, 1991, 5 (02) :489-493
[4]   Antigenic variation and allelic exclusion [J].
Borst, P .
CELL, 2002, 109 (01) :5-8
[5]   PCR fidelity of Pfu DNA polymerase and other thermostable DNA polymerases [J].
Cline, J ;
Braman, JC ;
Hogrefe, HH .
NUCLEIC ACIDS RESEARCH, 1996, 24 (18) :3546-3551
[6]  
CUSHION MT, 1989, J PROTOZOOL, V36, P45
[7]   METHOD OF TESTING THE SUSCEPTIBILITY OF PNEUMOCYSTIS-CARINII TO ANTIMICROBIAL AGENTS INVITRO [J].
CUSHION, MT ;
STANFORTH, D ;
LINKE, MJ ;
WALZER, PD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1985, 28 (06) :796-801
[8]   GROWTH AND METABOLISM OF PNEUMOCYSTIS-CARINII IN AXENIC CULTURE [J].
CUSHION, MT ;
EBBETS, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (06) :1385-1394
[9]   PNEUMOCYSTIS-CARINII - GROWTH VARIABLES AND ESTIMATES IN THE A549 AND WI-38 VA13 HUMAN CELL-LINES [J].
CUSHION, MT ;
RUFFOLO, JJ ;
LINKE, MJ ;
WALZER, PD .
EXPERIMENTAL PARASITOLOGY, 1985, 60 (01) :43-54
[10]   GROWTH AND SERIAL PASSAGE OF PNEUMOCYSTIS-CARINII IN THE A549 CELL-LINE [J].
CUSHION, MT ;
WALZER, PD .
INFECTION AND IMMUNITY, 1984, 44 (02) :245-251