Rickettsia prowazeki, the etiological agent of epidemic typhus, is unusual, even amongst the intracellular bacterial parasites, inthat it grows in the cytoplasm, rather than in a vacuole, of its eukaryotic host. Hence, our focus has been to ask what are the biochemical and physiological mechanisms by which this organism copes whith the problems and exploits the opportunities of this unique environmental niche and what are the mechanisms by which the rickettsiae enter the host cell's cytoplasm. There are three general areas that we intend to investigate during the next five years. 1) The transport systems for those nutrients that the rickettsia encounters in the cytoplasm. This area includes the study of NAD(H), ATP/ADP and amino acids translocases and the development of a membrane vesicle system. 2) The metabolic capabilities of R. prowazeki and the regulation of these processes. The role of ATP/ADP in regulation of rickettsial enzymes and use of somatic cell mutants to explore rickettsial metabolism are key features of this area. 3) The penetration of eukaryotic cells by the rickettsia as determined both in a model system with erythrocytes and in a productive system with competent host cells. The role of the phospholipase A activity and an elucidation of binding sites in rickettsia-host interactions are included in this area. All these areas are highly interrelated and projects with a lengthy development phase are interspersed with those that are straight forward.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI015035-08
Application #
3125989
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1979-01-01
Project End
1986-02-28
Budget Start
1985-01-01
Budget End
1986-02-28
Support Year
8
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of South Alabama
Department
Type
Schools of Medicine
DUNS #
City
Mobile
State
AL
Country
United States
Zip Code
36688
Housley, Nicole A; Winkler, Herbert H; Audia, Jonathon P (2011) The Rickettsia prowazekii ExoU homologue possesses phospholipase A1 (PLA1), PLA2, and lyso-PLA2 activities and can function in the absence of any eukaryotic cofactors in vitro. J Bacteriol 193:4634-42
Audia, Jonathon P; Winkler, Herbert H (2006) Study of the five Rickettsia prowazekii proteins annotated as ATP/ADP translocases (Tlc): Only Tlc1 transports ATP/ADP, while Tlc4 and Tlc5 transport other ribonucleotides. J Bacteriol 188:6261-8
Audia, Jonathon P; Roberts, Rosemary A W; Winkler, Herbert H (2006) Cysteine-scanning mutagenesis and thiol modification of the Rickettsia prowazekii ATP/ADP translocase: characterization of TMs IV-VII and IX-XII and their accessibility to the aqueous translocation pathway. Biochemistry 45:2648-56
Alexeyev, Mikhail F; Roberts, Rosemary A W; Daugherty, Robin M et al. (2004) Cysteine-scanning mutagenesis and thiol modification of the Rickettsia prowazekii ATP/ADP translocase: evidence that transmembrane regions I and II, but not III, are structural components of the aqueous translocation channel. Biochemistry 43:6995-7002
Daugherty, Robin M; Linka, Nicole; Audia, Jonathon P et al. (2004) The nucleotide transporter of Caedibacter caryophilus exhibits an extended substrate spectrum compared to the analogous ATP/ADP translocase of Rickettsia prowazekii. J Bacteriol 186:3262-5
Linka, Nicole; Hurka, Herbert; Lang, B Franz et al. (2003) Phylogenetic relationships of non-mitochondrial nucleotide transport proteins in bacteria and eukaryotes. Gene 306:27-35
Schwoppe, Christian; Winkler, Herbert H; Neuhaus, H Ekkehard (2003) Connection of transport and sensing by UhpC, the sensor for external glucose-6-phosphate in Escherichia coli. Eur J Biochem 270:1450-7
Winkler, Herbert H; Daugherty, Robin M; Audia, Jonathon P (2003) Cysteine-scanning mutagenesis and thiol modification of the Rickettsia prowazekii ATP/ADP translocase: evidence that TM VIII faces an aqueous channel. Biochemistry 42:12562-9
Alexeyev, Mikhail F; Winkler, Herbert H (2002) Complete replacement of basic amino acid residues with cysteines in Rickettsia prowazekii ATP/ADP translocase. Biochim Biophys Acta 1565:136
Schwoppe, Christian; Winkler, Herbert H; Neuhaus, H Ekkehard (2002) Properties of the glucose-6-phosphate transporter from Chlamydia pneumoniae (HPTcp) and the glucose-6-phosphate sensor from Escherichia coli (UhpC). J Bacteriol 184:2108-15

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