Dr. Austin Nuxoll

Associate Professor

办公室: 黑洞 201D | 电话: (308) 865-8602 | 电子邮件: nuxollas@firstnews-extra.com

传记

Areas of Interest:

Microbial Pathogenesis, Host-Pathogen Interactions, Antibiotic Tolerance

度:

B.S. (2009) - University of Nebraska at Kearney
博士学位. (2014) - University of Nebraska Medical Center

Professional Affiliations:

Dissertation:

纳克叟,. S. 2009. Arginine Biosynthesis in Staphylococcus aureus. Ph. D. Dissertation, University of Nebraska Medical Center, Omaha, Nebraska. 193 pp.

Publications:

霍布斯,.M.Kluthe, K.E., Carlson, K.A., 纳克叟,.S. 2021. Interruption of the tricarboxylic acid cycle in Staphylococcus aureus leads to increased tolerance in innate immunity. AIMS Microbiology 7(4):513-527. doi: 10.3934/microbiol.2021031
Nabb D.L.，宋，S.Kluthe, K.E., Daubert, T.A., Luedtke, B.E., 纳克叟,.S. 2019. Polymicrobial interactions induce multidrug tolerance in Staphylococcus aureus through energy depletion. Frontiers in Microbiology 10(2803).
Zalis E.A., 纳克叟,.S.Manuse, S.，克莱尔，G., Radlinski, L.C.康伦，B.P.阿德金斯，J.刘易斯，K. 2019. Stochastic variation in expression of the tricarboxylic acid cycle produces persister cells. mBio 10:e01930-19.
哈尔西,C.R.李磊，S.， Wax, J.K., Lehman, M.K., 纳克叟,.S., Steinke L., Sadykov, M.幂幂R., Fey, P.D. 2017. Amino acid catabolism in Staphylococcus aureus and the function of carbon catabolite repression. mBio 8(1) pii: e01434-16.
Homma T., 纳克叟,., Brown-Gandt, A.P.，恩格斯，我., Schneider, T.格茨，F.刘易斯，K., 康伦,B. P. 2016. Dual targeting of cell wall precursors by teixobactin leads to cell lysis. AAC格式 doi: 10.1128 / AAC格式格式.01050-16 AAC格式.01050-16.

康伦,B.P.罗，S.E.甘特，A.B., 纳克叟,.S., 数日,N.P.， Zalis E.A.，克莱尔，G.阿德金斯，J.N.张，A.L., Lewis, K. 2016. Persister formation in Staphylococcus aureus is associated with ATP depletion. Nat Microbiol doi: 10.1038/nmicrobiol.2016.51
林格伦,J.K.托马斯·V.C.奥尔森，M.E., Chaudhari, S.S., 纳克叟,.S., Schaeffer, C.R., Lindgren, K.E.琼斯，J., Zimmerman, M.C.邓曼，P.D.贝利斯，K.W., Fey, P.D. 2014. Arginine deiminase in Staphylococcus epidermidis functions to augment biofilm maturation through pH homeostasis. J Bacteriol 196(12): 2277-89.
葛瑞斯C.M.玻色，J.L., 纳克叟,.S.菲，P.D., •贝勒斯K. W. 2013. The Ktr potassium transport system in Staphylococcus aureus and its role in cell physiology, antimicrobial resistance, pathogenesis. 摩尔微 89(4): 760-73.
Maliszewski, K.L., 纳克叟,.S. 2013. Use of electroporation and conjugative mobilization for genetic manipulation of Staphylococcus epidermidis. Methods Mol Biol 1106: 125-134.
Sadykov, M.R., 托马斯,V.C., 马歇尔,维.D., Wenstrom C.J., Moormeier, D.E., Widhelm T.J., 纳克叟,.S., 权力,R., •贝勒斯K. W. 2013. Inactivation of the Pta-AckA pathway causes cell death in Staphylococcus aureus. J Bacteriol. 195(13): 3035-44.
纳克叟,.S., Halouska, S.M., Sadykov, M.R.汉克，M.L.贝利斯，K.W., Kielian, T.幂幂R., Fey, P.D. 2012. CcpA regulates arginine biosynthesis in Staphylococcus aureus through repression of proline catabolism. 公共科学图书馆Pathog 8(11): e1003033.