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Biofilm in group A streptococcal necrotizing soft tissue infections
Nikolai Siemens, … , Mattias Svensson, Anna Norrby-Teglund
Nikolai Siemens, … , Mattias Svensson, Anna Norrby-Teglund
Published July 7, 2016
Citation Information: JCI Insight. 2016;1(10):e87882. https://doi.org/10.1172/jci.insight.87882.
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Research Article Infectious disease

Biofilm in group A streptococcal necrotizing soft tissue infections

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Abstract

Necrotizing fasciitis caused by group A streptococcus (GAS) is a life-threatening, rapidly progressing infection. At present, biofilm is not recognized as a potential problem in GAS necrotizing soft tissue infections (NSTI), as it is typically linked to chronic infections or associated with foreign devices. Here, we present a case of a previously healthy male presenting with NSTI caused by GAS. The infection persisted over 24 days, and the surgeon documented the presence of a “thick layer biofilm” in the fascia. Subsequent analysis of NSTI patient tissue biopsies prospectively included in a multicenter study revealed multiple areas of biofilm in 32% of the patients studied. Biopsies associated with biofilm formation were characterized by massive bacterial load, a pronounced inflammatory response, and clinical signs of more severe tissue involvement. In vitro infections of a human skin tissue model with GAS NSTI isolates also revealed multilayered fibrous biofilm structures, which were found to be under the control of the global Nra gene regulator. The finding of GAS biofilm formation in NSTIs emphasizes the urgent need for biofilm to be considered as a potential complicating microbiological feature of GAS NSTI and, consequently, emphasizes reconsideration of antibiotic treatment protocols.

Authors

Nikolai Siemens, Bhavya Chakrakodi, Srikanth Mairpady Shambat, Marina Morgan, Helena Bergsten, Ole Hyldegaard, Steinar Skrede, Per Arnell, Martin B. Madsen, Linda Johansson, INFECT Study Group, Julius Juarez, Lidija Bosnjak, Matthias Mörgelin, Mattias Svensson, Anna Norrby-Teglund

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Figure 7

Role of Nra and Sortase A in biofilm formation in the tissue setting.

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Role of Nra and Sortase A in biofilm formation in the tissue setting.
(A...
(A) Amounts of capsular hyaluronic acid in exponential growth phase bacteria. The horizontal line denotes mean values of the 3 experiments. (B) Western Blot analysis of secreted SpeB by indicated strains at late stationary growth stage. Representative image of 3 experiments is shown (n = 3). Original blot is shown in Supplemental Figure 7. (C) CFU counts of indicated bacteria recovered from tissue models after 48 hours of infection. The horizontal line denotes mean values (n = 3). (D) Blinded scoring of tissue pathology of the skin model after infection. Each symbol represents one independent experiment. Horizontal lines denote median values (n = 3). (E) Relative mRNA expression of the transcriptional regulator nra is shown. The data represent the mean values ± SD (n = 3). (F) Representative immunofluorescence images of biofilm after 48 hours of infection (original magnification, ×100). GAS-specific antibody, wheat germ agglutinin (WGA), and Nile red were used.

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