In an effort to study the role of Borrelia burgdorferi proteins whose expression respond to changes in culture temperature, strain Sh-2-82 spirochetes were serially passaged 16 times in vitro. Following serial passage, the protein and plasmid DNA profiles of the passage 16 variant were compared with that of the low-passage (passage 3) parental culture to assess the loss of protein expression and plasmid DNAs. The expression of 16 antigens in the parental culture was found to be selectively induced at the higher incubation temperature of 34?C and not at the lower temperature of 24?C. A majority of the 16 parental antigens were subsequently lost in the higher passage variant. The loss of expression of these antigens in the higher passage variant also correlated with the loss of infectivity for the C3H/HeN mouse. Two of the 16 antigens were identified as the lipoproteins OspC, an antigen previously known to be temperature-inducible (Stevenson, B. T. G. Schwan, and P. A. Rosa, Infect. Immun. 63:4535-4539, 1995) and P35. The loss of antigen expression could not be correlated, however, with a detectable loss of plasmid sequences; specifically, the plasmids carrying the ospC and P35 genes were both found to be retained in the passage 16 variant. The temperature-inducible expression of OspC and P35 in the parental Sh-2-82 spirochetes and their minimal levels of expression in the passage 16 variant, both correlated with the steady state levels of the corresponding mRNAs. These data suggest that temperature-inducible antigens are essential for infectivity and that the regulated expression of at least two of these antigens, OspC and P35, is controlled at the transcriptional level. FUNDING Base PUBLICATIONS None

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000164-38
Application #
6116203
Study Section
Project Start
1999-05-01
Project End
2000-04-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Tulane University
Department
Type
DUNS #
City
New Orleans
State
LA
Country
United States
Zip Code
70118
Mahalingam, Ravi; Kaufer, Benedikt B; Ouwendijk, Werner J D et al. (2018) Attenuation of Simian Varicella Virus Infection by Enhanced Green Fluorescent Protein in Rhesus Macaques. J Virol 92:
Kumar, Vinay; Mansfield, Joshua; Fan, Rong et al. (2018) miR-130a and miR-212 Disrupt the Intestinal Epithelial Barrier through Modulation of PPAR? and Occludin Expression in Chronic Simian Immunodeficiency Virus-Infected Rhesus Macaques. J Immunol 200:2677-2689
Parthasarathy, Geetha; Philipp, Mario T (2018) Intracellular TLR7 is activated in human oligodendrocytes in response to Borrelia burgdorferi exposure. Neurosci Lett 671:38-42
McNamara, Ryan P; Costantini, Lindsey M; Myers, T Alix et al. (2018) Nef Secretion into Extracellular Vesicles or Exosomes Is Conserved across Human and Simian Immunodeficiency Viruses. MBio 9:
Yi, Fei; Guo, Jia; Dabbagh, Deemah et al. (2017) Discovery of Novel Small-Molecule Inhibitors of LIM Domain Kinase for Inhibiting HIV-1. J Virol 91:
Jorgensen, Matthew J; Lambert, Kelsey R; Breaux, Sarah D et al. (2017) Pair housing of Vervets/African Green Monkeys for biomedical research. Am J Primatol 79:1-10
Ramesh, Geeta; Martinez, Alejandra N; Martin, Dale S et al. (2017) Effects of dexamethasone and meloxicam on Borrelia burgdorferi-induced inflammation in glial and neuronal cells of the central nervous system. J Neuroinflammation 14:28
Parthasarathy, Geetha; Philipp, Mario T (2017) Receptor tyrosine kinases play a significant role in human oligodendrocyte inflammation and cell death associated with the Lyme disease bacterium Borrelia burgdorferi. J Neuroinflammation 14:110
Calenda, Giulia; Villegas, Guillermo; Barnable, Patrick et al. (2017) MZC Gel Inhibits SHIV-RT and HSV-2 in Macaque Vaginal Mucosa and SHIV-RT in Rectal Mucosa. J Acquir Immune Defic Syndr 74:e67-e74
Datta, Dibyadyuti; Bansal, Geetha P; Grasperge, Brooke et al. (2017) Comparative functional potency of DNA vaccines encoding Plasmodium falciparum transmission blocking target antigens Pfs48/45 and Pfs25 administered alone or in combination by in vivo electroporation in rhesus macaques. Vaccine 35:7049-7056

Showing the most recent 10 out of 352 publications