Ultraviolet C light for Acinetobacter baumannii wound infections in mice: potential use for battlefield wound decontamination?
Ultraviolet C light for Acinetobacter baumannii wound infections in mice: potential use for battlefield wound decontamination?
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紫外线 C 光治疗小鼠鲍曼不动杆菌伤口感染:战场伤口净化的潜在用途?
DOI:
10.1097/ta.0b013e31825c149c
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发表时间:
2012-09
期刊:
影响因子:
--
通讯作者:
Hamblin MR
中科院分区:
文献类型:
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作者:
Dai T;Murray CK;Vrahas MS;Baer DG;Tegos GP;Hamblin MR
Since the beginning of the conflicts in the Middle East, US Army physicians have noted a high rate of multidrug-resistant Acinetobacter baumannii infections among US soldiers wounded and initially treated in Iraq. In this study, we investigated the use of ultraviolet C (UVC) light for prevention of multidrug-resistant A. baumannii wound infections using mouse models. Partial-thickness skin abrasions and full-thickness burns in mice were infected with a multidrug-resistant A. baumannii isolate recovered from a wounded US soldier deployed to Iraq. The luxCDABE operon, which was contained in plasmid pMF 385, was cloned into the A. baumannii strain. This allowed real-time monitoring of the extent of infection in mice using bioluminescence imaging. UVC light was delivered to the mouse wounds at 30 minutes after the inoculation of A. baumannii. Groups of infected mouse wounds without being exposed to UVC served as the controls. In vitro studies demonstrated that A. baumannii cells were inactivated at UVC exposures much lower than those needed for a similar effect on mammalian cells. It was observed in animal studies that UVC (3.24 J/cm2 for abrasions and 2.59 J/cm2 for burns) significantly reduced the bacterial burdens in UVC-treated wounds by approximately 10-fold compared with nontreated controls (p = 0.004 for abrasions, p = 0.019 for burns). DNA lesions were observed by immunofluorescence in mouse skin abrasions immediately after a UVC exposure of 3.24 J/cm2; however, the lesions were extensively repaired within 72 hours. These results suggested that UVC may be useful in preventing combat-related wound infections.