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Signaling by two-component system noncognate partners promotes intrinsic tolerance to polymyxin B in uropathogenic Escherichia coli
被引:31
作者:
Guckes, Kirsten R.
[1
]
Breland, Erin J.
[2
]
Zhang, Ellisa W.
[1
]
Hanks, Sarah C.
[3
]
Gill, Navleen K.
[4
]
Algood, Holly M. S.
[1
,5
,6
]
Schmitz, Jonathan E.
[1
]
Stratton, Charles W.
[1
,5
]
Hadjifrangiskou, Maria
[1
,7
]
机构:
[1] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Pharmacol, Nashville, TN 37232 USA
[3] Barnard Coll, New York, NY 10027 USA
[4] Vanderbilt Univ, Nashville, TN 37240 USA
[5] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN 37232 USA
[6] Vet Affairs Tennessee Valley Healthcare Serv, Nashville, TN 37212 USA
[7] Vanderbilt Univ, Med Ctr, Dept Urol Surg, Nashville, TN 37232 USA
基金:
美国国家科学基金会;
关键词:
ENTERICA SEROVAR TYPHIMURIUM;
QSEB RESPONSE REGULATOR;
SALMONELLA-ENTERICA;
SENSOR KINASE;
TRANSDUCTION PATHWAYS;
BACTERIAL CHEMOTAXIS;
COGNATE SENSOR;
CROSS-TALK;
C QSEBC;
ACTIVATION;
D O I:
10.1126/scisignal.aag1775
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Bacteria use two-component systems (TCSs) to react appropriately to environmental stimuli. Typical TCSs comprise a sensor histidine kinase that acts as a receptor coupled to a partner response regulator that coordinates changes in bacterial behavior, often through its activity as a transcriptional regulator. TCS interactions are typically confined to cognate pairs of histidine kinases and response regulators. We describe two distinct TCSs in uropathogenic Escherichia coli (UPEC) that interact to mediate a response to ferric iron. The PmrAB and QseBC TCSs were both required for proper transcriptional response to ferric iron. Ferric iron induced the histidine kinase PmrB to phosphotransfer to both its cognate response regulator PmrA and the noncognate response regulator QseB, leading to transcriptional responses coordinated by both regulators. Pretreatment of the UPEC strain UTI89 with ferric iron led to increased resistance to polymyxin B that required both PmrA and QseB. Similarly, pretreatment of several UPEC isolates with ferric iron increased tolerance to polymyxin B. This study defines physiologically relevant cross-talk between TCSs in a bacterial pathogen and provides a potential mechanism for antibiotic resistance of some strains of UPEC.
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页数:9
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