Abstract
Acinetobacter baumannii is considered a problematic Gram-negative pathogen due to its widespread resistance to antibiotics. Understanding of resistance mechanisms in A. baumannii is critical for designing new and effective therapeutic options. However, this is hampered by the lack of tools to carry out genetic manipulations in A. baumannii. Here, we describe methods to use a chromosomal mini-Tn7-based single-copy gene expression system in A. baumannii. This system can be effectively used for performing genetic complementation studies, for tagging with fluorescent proteins, or for reporter fusion assays.
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Acknowledgments
This work was supported by grants from the Natural Sciences and Engineering Council of Canada (NSERC, 2015-05550) and the Canadian Institutes of Health Research (CIHR, 201610PJT-376486) to AK. Original work in the HPS laboratory was funded in part by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under Award Number U54 AI065357. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
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Ducas-Mowchun, K., De Silva, P.M., Patidar, R., Schweizer, H.P., Kumar, A. (2019). Tn7-Based Single-Copy Insertion Vectors for Acinetobacter baumannii. In: Biswas, I., Rather, P. (eds) Acinetobacter baumannii. Methods in Molecular Biology, vol 1946. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-9118-1_13
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DOI: https://doi.org/10.1007/978-1-4939-9118-1_13
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