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Research advances understanding of defenses against antibiotic-resistant klebsiella bacteria

Date:
January 25, 2017
Source:
NIH/National Institute of Allergy and Infectious Diseases
Summary:
Klebsiella bacteria cause about 10 percent of all hospital-acquired infections in the United States. K. pneumoniae sequence type 258 (ST258) is one of the Carbapenem-Resistant Enterobacteriaceae organisms labeled an urgent threat by the Centers for Disease Control and Prevention. This strain of bacteria is particularly concerning because it is resistant to most antibiotics and kills nearly half of people with bloodstream infections. Scientists seeking alternatives to antibiotics report that an antibody-based therapy approach may be useful against ST258 bacteria.
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Klebsiella bacteria cause about 10 percent of all hospital-acquired infections in the United States. K. pneumoniae sequence type 258 (ST258) is one of the Carbapenem-Resistant Enterobacteriaceae organisms labeled an urgent threat by the Centers for Disease Control and Prevention. This strain of bacteria is particularly concerning because it is resistant to most antibiotics and kills nearly half of people with bloodstream infections.

National Institutes of Health (NIH) scientists and their colleagues seeking alternatives to antibiotics report that an antibody-based therapy approach may be useful against ST258 bacteria. Studies of modified human blood samples showed that a component of the innate immune system called the complement system is pivotal to killing ST258. The complement system includes nine proteins (C1-9) that help protect against bacterial infections, a process aided by antibodies.

Their study determined that killing of ST258 corresponds with a portion of the complement system known as the membrane attack complex (C5b-C9), which contacts bacterial surfaces. Blood depleted of antibodies and/or the complement system had a significantly reduced ability to kill antibiotic-resistant ST258 bacteria.

The scientists, ultimately hoping to develop new tools to treat and prevent these infections, now plan to test a modified antibody against ST258 in laboratory blood and animal infection models. They also plan to learn more about the complement system in people with K. pneumoniae bloodstream infections. They note that ST258 bacteria reside harmlessly in most healthy people; infection is usually of significant concern only for those in healthcare settings suffering from co-existing conditions or diseases.


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Materials provided by NIH/National Institute of Allergy and Infectious Diseases. Note: Content may be edited for style and length.


Journal Reference:

  1. Frank R. DeLeo, Scott D. Kobayashi, Adeline R. Porter, Brett Freedman, David W. Dorward, Liang Chen, Barry N. Kreiswirth. Survival of carbapenem-resistant ST258 Klebsiella pneumoniae in human blood. Antimicrobial Agents and Chemotherapy, 2017; AAC.02533-16 DOI: 10.1128/AAC.02533-16

Cite This Page:

NIH/National Institute of Allergy and Infectious Diseases. "Research advances understanding of defenses against antibiotic-resistant klebsiella bacteria." ScienceDaily. ScienceDaily, 25 January 2017. <www.sciencedaily.com/releases/2017/01/170125120735.htm>.
NIH/National Institute of Allergy and Infectious Diseases. (2017, January 25). Research advances understanding of defenses against antibiotic-resistant klebsiella bacteria. ScienceDaily. Retrieved May 29, 2017 from www.sciencedaily.com/releases/2017/01/170125120735.htm
NIH/National Institute of Allergy and Infectious Diseases. "Research advances understanding of defenses against antibiotic-resistant klebsiella bacteria." ScienceDaily. www.sciencedaily.com/releases/2017/01/170125120735.htm (accessed May 29, 2017).

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