In recent years, a massive increase in the rates of antibiotic resistant bacteria has been observed in clinical settings, causing significant concern from both the scientific community and government agencies. Among the pathogens causing these alarming infections is Acinetobacter baumannii, a microorganism that has developed resistance to almost all available antibiotics. Its extreme genome plasticity, largely facilitated by horizontal genetic transfer (HGT) processes, has contributed to its remarkable antibiotic-resistance phenotype. Transformation seems to be a particularly important HGT mechanism in this bacterium. However, the environmental signals triggering competence for natural transformation, the putative effectors involved in this process, and the molecular basis of this phenomenon are still poorly understood. Using the A. baumannii A118 clinical isolate as a model, the proposed project will examine the role of human host products as chemical inducers of DNA uptake. Considering our preliminary data, which show that different albumins cause a significant increase in the level of transformation frequency, this study will examine the role of Human Serum Albumin (HSA) and albumin-derived peptides in the development of bacterial competence and the uptake of foreign DNA (Aim 1). Moreover, we will determine the effects of HSA using a whole-genome transcriptional profiling approach in A118 (Aim 2). Through this last approach, we expect to identify genes and RNA regulators involved in natural transformation. This knowledge will provide critical insights into the molecular and cellular mechanism this pathogen uses to acquire resistance genes. Future studies can then use these findings to develop novel approaches to treat severe Acinetobacter human infections, particularly those caused by emerging multidrug-resistant isolates.

Public Health Relevance

The emergence of bacterial pathogens with extreme levels of antibiotic resistance, such as Acinetobacter baumannii, have posed a serious threat to human health worldwide. This project will examine the role that host-related environmental signals play in the ability of A. baumannii to emerge as an untreatable pathogen and identify genes coding for structural functions and regulatory elements that contribute to the acquisition of antibiotic resistance of this bacterium. Knowledge gained from this study would potentially identify targets for the development of novel approaches to control the antibiotic resistance of A. baumannii.

National Institute of Health (NIH)
National Institute of General Medical Sciences (NIGMS)
Research Continuance Award (SC3)
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Special Emphasis Panel (ZGM1)
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Rubio, Mercedes
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California State University Fullerton
Schools of Arts and Sciences
United States
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Martinez, Jasmine; Liu, Christine; Rodman, Nyah et al. (2018) Human fluids alter DNA-acquisition in Acinetobacter baumannii. Diagn Microbiol Infect Dis :
MontaƱa, S; Fernandez, J S; Barenboim, M et al. (2018) Whole-genome analysis and description of an outbreak due to carbapenem-resistant Ochrobactrum anthropi causing pseudo-bacteraemias. New Microbes New Infect 26:100-106
Quinn, Brettni; Rodman, Nyah; Jara, Eugenio et al. (2018) Human serum albumin alters specific genes that can play a role in survival and persistence in Acinetobacter baumannii. Sci Rep 8:14741