The genus Rickettsia, including Rickettsia prowazekii, the etiological agent of epidemic typhus, is unique, even amongst the intracellular bacterial parasites. These organisms grow directly in the cytoplasm, rather than in a vacuole in the cytoplasm of their eukaryotic host cells. We remain intensely interested in the biochemical and physiological mechanisms by which this organism copes with the problems and exploits the opportunities of this unique environmental niche and seek to define the mechanisms by which the rickettsiae enter the host cell cytoplasm. During the next five years we hope to answer key questions concerning 1) the transport systems for those nutrients that the rickettsia encounters in the cytoplasm, the metabolic capabilities of R. prowazekii for these substrates and the regulation of these processes; 2) the penetration mechanism used by rickettsiae to infect eukaryotic cells with emphasis on both the receptor interactions and the phospholipase A activity.
The specific aims encompassed in these general areas are: I. Transport systems and metabolism: a) Development of the """"""""rickettsiae with protein synthesis"""""""" as a system for transport studies of amino acids; b) Utilization of the corresponding """"""""rickettsiae with m-RNA synthesis"""""""" to define the pathway for net ribonucleotide transport; c) Characterization of the ATP/ADP transport system in membrane vesicles using the cloned and expressed gene in E. coli; d) Investigation of growth and metabolism of rickettsiae growing in transport and respiratory-deficient somatic cell mutants; e) Characterization of the transport and metabolism of nucleotide sugars as a possible strategy for carbohydrate metabolism of nucleotide glycolytic enzymes; f) Investigation of proton translocation and its relationship to proton motive force in rickettsiae. II. Penetration-Receptors and Phospholipase A: a) Investigation of the role of phospholipase A2 activity in lysis of and entry into host cells; b) Characterization of receptors of the host-cell involved in rickettsia-host recognition using the Fluorescence Activated Cell Sorter.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI015035-11
Application #
3125991
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1979-01-01
Project End
1989-12-31
Budget Start
1988-01-01
Budget End
1988-12-31
Support Year
11
Fiscal Year
1988
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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