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Tasked with a Challenging Objective: Why Do Neutrophils Fail to Battle Pseudomonas aeruginosa Biofilms

1
Molecular and Cellular Biology Department, University of Guelph, Guelph, ON N1G 2W1, Canada
2
Division of Infectious Diseases, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA
*
Author to whom correspondence should be addressed.
Pathogens 2019, 8(4), 283; https://doi.org/10.3390/pathogens8040283
Received: 25 October 2019 / Revised: 26 November 2019 / Accepted: 2 December 2019 / Published: 4 December 2019
(This article belongs to the Special Issue Pathogenesis of Fungal and Bacterial Microbes)
Multidrug-resistant (MDR) bacterial infections are a leading cause of mortality, affecting approximately 250,000 people in Canada and over 2 million people in the United States, annually. The lack of efficacy of antibiotic-based treatments is often caused by inability of the drug to penetrate bacterial biofilms in sufficient concentrations, posing a major therapeutic challenge. Here, we review the most recent information about the architecture of Pseudomonas aeruginosa biofilms in vivo and describe how advances in imaging and mass spectroscopy analysis bring about novel therapeutic options and challenge existing dogmas. View Full-Text
Keywords: neutrophils; biofilms; therapies; enzymes neutrophils; biofilms; therapies; enzymes
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Geddes-McAlister, J.; Kugadas, A.; Gadjeva, M. Tasked with a Challenging Objective: Why Do Neutrophils Fail to Battle Pseudomonas aeruginosa Biofilms. Pathogens 2019, 8, 283.

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