Most mycoplasma species with polarized cell morphologies exhibit gliding motility, a process inextricably intertwined with adherence to host cells (cytadherence) but of uncertain molecular mechanism. Moreover, different phylogenetic groups of mycoplasmas appear to adhere and glide by different mechanisms. Mycoplasma penetrans, an organism found principally in HIV-positive patients in whom it appears to potentiate the progress of AIDS by promoting proliferation of the type of cell that HIV infects, also exhibits polar morphology and is known to burrow into host epithelial cells. However, the molecular basis for its interaction with host cells is entirely unknown, its genome sequence indicating an absence of homologs of cytadherence proteins of other organisms. We have established that three different M. penetrans strains exhibit gliding motility and adherence with positive correlation between speed and strength of adherence. We have identified a detergent-insoluble structure in the leading, adherence-associated cell pole and two of its probable protein components. We will continue to identify components of this cell polarity-associated structure by mass spectrometry of detergent-insoluble proteins as well as by testing whether similar proteins encoded by adjacent genes are components. We will examine the expression of polarity-associated genes to determine whether they are cotranscribed, and we will identify further virulence-associated genes of M. penetrans through microarray data, comparing bacteria grown axenically with bacteria grown in the presence of host cells. Finally, we will obtain genome sequences for the two M. penetrans strains that are not yet sequenced, and use comparative analysis to identify candidate genes for adhesins and motor proteins. The results of these experiments will shed light on generation of cellular polarity, cellular motility, and the means by which M. penetrans might contribute to the sickness of AIDS patients in hopes of rational design of inhibitors of this likely cofactor.

Public Health Relevance

Although for some bacteria it is understood how they move and how they attach to the cells of people they infect, mycoplasmas behave differently from other bacteria, and different types of mycoplasmas behave differently from one another. Mycoplasma penetrans is usually found in patients infected with HIV, which causes AIDS, and is believed to cause those patients'disease to progress faster than individuals without M. penetrans infection. In this study, we will identify molecules associated with adherence of M. penetrans to the cells of its host, movement of M. penetrans, and the ability of M. penetrans to cause disease in general.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
2R15AI073994-02
Application #
8097060
Study Section
Prokaryotic Cell and Molecular Biology Study Section (PCMB)
Program Officer
Taylor, Christopher E,
Project Start
2007-04-01
Project End
2014-05-31
Budget Start
2011-06-01
Budget End
2014-05-31
Support Year
2
Fiscal Year
2011
Total Cost
$314,880
Indirect Cost
Name
Miami University Oxford
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
041065129
City
Oxford
State
OH
Country
United States
Zip Code
45056
Distelhorst, Steven L; Jurkovic, Dominika A; Shi, Jian et al. (2017) The Variable Internal Structure of the Mycoplasma penetrans Attachment Organelle Revealed by Biochemical and Microscopic Analyses: Implications for Attachment Organelle Mechanism and Evolution. J Bacteriol 199:
Pritchard, Rachel E; Balish, Mitchell F (2015) Mycoplasma iowae: relationships among oxygen, virulence, and protection from oxidative stress. Vet Res 46:36
Balish, Mitchell F (2014) Mycoplasma pneumoniae, an underutilized model for bacterial cell biology. J Bacteriol 196:3675-82
Pritchard, Rachel E; Prassinos, Alexandre J; Osborne, John D et al. (2014) Reduction of hydrogen peroxide accumulation and toxicity by a catalase from Mycoplasma iowae. PLoS One 9:e105188
Jurkovic, Dominika A; Hughes, Michael R; Balish, Mitchell F (2013) Analysis of energy sources for Mycoplasma penetrans gliding motility. FEMS Microbiol Lett 338:39-45
Jurkovic, Dominika A; Newman, Jaime T; Balish, Mitchell F (2012) Conserved terminal organelle morphology and function in Mycoplasma penetrans and Mycoplasma iowae. J Bacteriol 194:2877-83
Relich, Ryan F; Balish, Mitchell F (2011) Insights into the function of Mycoplasma pneumoniae protein P30 from orthologous gene replacement. Microbiology 157:2862-70
Relich, Ryan F; Friedberg, Aaron J; Balish, Mitchell F (2009) Novel cellular organization in a gliding mycoplasma, Mycoplasma insons. J Bacteriol 191:5312-4