切换到宽版

 找回密码
 注册

微信登录,快人一步

QQ登录

只需一步,快速开始

查看: 1333|回复: 4

[国际资讯] 超级细菌不再无药可用

[复制链接]
发表于 2017-9-25 16:52:38 | 显示全部楼层 |阅读模式
感控热点丨超级细菌不再无药可用

原创 2017-09-22 翻译:周超群 SIFIC感染官微
检索:刘金淑
翻译:周超群
审核: 刘金淑、陈志锦
file:///C:/Users/lenovo/AppData/Local/Temp/msohtmlclip1/01/clip_image001.gif
美国:研究人员联合使用抗菌药物首次杀灭高耐药性大肠埃希菌

由布法罗大学道格拉斯·雷维尔(Douglas Levere)提供的研究信息,氨曲南、阿米卡星和多粘菌素B的新型组合能够杀死携带mcr-1和ndm-5基因的大肠埃希菌,这两种基因使细菌能突破最后一道抗生素防线。
抗生素的黄金时代可能即将结束。最近发现携带mcr-1和ndm-5基因的大肠埃希菌使得细菌对最后抗生素免疫,已经导致临床医生无有效的手段来治疗超级细菌。但是在一项新的研究中,布法罗大学的研究人员组合了三种抗生素,它们在一起能铲除致命细菌。这一开创性的研究最近发表在美国微生物学会杂志《mBio》上。
研究人员发现,由氨曲南、阿米卡星和被称为抗生素最后防线之一的多粘菌素B的新型组合能够在24小时内杀死携带mcr-1和ndm-5基因的大肠埃希菌,同时也能防止它们的再次生长。然而,这些抗生素的传统组合并不能杀死这种大肠埃希菌,反而导致快速耐药性。
尽管在美国已报道的携带mcr-1的大肠埃希菌病例不到24例,但随着世界各地报告的病例数的增加,细菌对可用抗生素的免疫力已使医疗界容易受到大规模感染暴发的伤害。
抗生素耐药菌的快速增长,使多粘菌素的重要性重新引起人们的关注,多粘菌素是对耐药菌有效的一类抗生素,但由于它可能对肾脏造成伤害,而被当作最后的抗生素治疗手段。
为了避免开出高剂量的多粘菌素并弥补其缺陷,研究人员决定采用新的给药策略和多种抗生素组合。研究人员研究了超过15种抗生素联合多粘菌素B的数十种组合后,发现了两种有效的治疗方法。多粘菌素B与氨曲南或阿米卡星的组合在24小时后检测不到细菌。
然而,大肠埃希菌数在96小时后能够再次达到初始水平,并且在暴露于多粘菌素B和阿米卡星组合的10天后,产生阿米卡星耐药菌株亚群。多粘菌素B和氨曲南能将大肠埃希菌抑制在持续但非复制状态。只有三联组合才能消除大肠埃希菌菌株并防止再生长。
这一重要发现有希望为mcr-1和ndm-5菌株提供可行的治疗方法。
资料来源:布法罗大学

原文:

Researchers Use Antibiotics Combo toKill First Strain of Highly Resistant E. coli in U.S.
August 21, 2017
A novel combination of aztreonam,amikacin and polymyxin B was able to kill E. coli carrying mcr-1 and ndm-5 —genes that make the bacterium immune to last-resort antibiotics. Courtesy ofDouglas Levere, University at Buffalo
The golden age of antibiotics may bedrawing to a close. The recent discovery of E. coli carrying mcr-1 and ndm-5 —genes that make the bacterium immune to last-resort antibiotics — has leftclinicians without an effective means of treatment for the superbug. But in anew study, University at Buffalo researchers have assembled a team of threeantibiotics that, together, are capable of eradicating the deadly bacterium.The groundbreaking research was recently published in mBio, a journal for theAmerican Society of Microbiology.
The researchers found that a novelcombination of aztreonam, amikacin and polymyxin B — a last-resort antibiotic —was able to kill E. coli carrying mcr-1 and ndm-5 genes within 24 hours whilealso preventing regrowth. Traditional combinations of these antibiotics wereunable to kill the E. coli and resulted in rapid resistance.
Fewer than two dozen cases of E. colicarrying mcr-1 have been reported in the U.S. However, with additional casesreported worldwide, the bacteria’s immunity to available antibiotics has leftthe medical community vulnerable to a massive outbreak of infections.
The rapid increase inantibiotic-resistant bacteria has resurrected the importance of polymyxins, aclass of antibiotics that are effective but employed as a last resort becauseof the damage they can cause to the kidneys.
To avoid prescribing high dosages ofpolymyxins and to make up for the antibiotic’s weaknesses, the researchersdecided to turn to new dosing strategies and multiple antibiotic combinations
After conducting studies on dozens ofcombinations of more than 15 antibiotics paired with polymyxin B, theresearchers discovered two effective treatments. Combinations of polymyxin Bwith either aztreonam or amikacin resulted in undetectable bacterial countsafter 24 hours.
The E. coli, however, was able to regrowto initial levels after 96 hours and a subpopulation of amikacin-resistantstrains arose after 10 days when exposed to the combination of polymyxin B andamikacin. Polymyxin B and aztreonam pushed the E. coli into a persistent butnonreplicating state. Only the triple combination eliminated the E. coli strainand prevented regrowth.
“We knew that polymyxins alone couldn’twork. Only the three drugs combined were able to work synergistically tosuppress and kill the bacteria,” says Bulman. “We overcame the bacteria bypushing it as far as possible with an agent that it was resistant to whilesimultaneously administering two other antibiotics.”
The promising finding may provide aviable treatment against mcr-1 and ndm-5 strains.
The research was funded through a $4.4million National Institutes of Health (NIH) grant awarded to Tsuji to developnew dosing regimens for polymyxins.
rce: University at Buffalo

图文编辑:小小牧童
审稿:马嘉睿 高晓东

发表于 2017-9-25 17:02:30 | 显示全部楼层
一个不错的消息。。,,
回复

使用道具 举报

发表于 2017-9-25 17:11:13 | 显示全部楼层
关键多粘菌素特别贵而且很难买到吧
回复

使用道具 举报

 楼主| 发表于 2017-9-25 18:12:17 来自手机 | 显示全部楼层
还可以,我们需要审批采购。
回复

使用道具 举报

发表于 2017-9-26 12:09:06 | 显示全部楼层
这样给多重耐药菌患者带来了福音!
回复

使用道具 举报

您需要登录后才可以回帖 登录 | 注册 |

本版积分规则

×本站发帖友情提示
1、注册用户在本社区发表、转载的任何作品仅代表其个人观点,不代表本社区认同其观点。
2、如果存在违反国家相关法律、法规、条例的行为,我们有权在不经作者准许的情况下删除其在本论坛所发表的文章、帖子。
3、所有网友不要盗用有明确版权要求的作品,转贴请注明来源,否则文责自负。
4、本社区保护注册用户个人资料,但是在自身原因导致个人资料泄露、丢失、被盗或篡改,本论坛概不负责,也不承担相应法律责任。

关闭

站长推荐上一条 /1 下一条

快速回复 返回顶部 返回列表