Eosinophil extracellular DNA traps: molecular mechanisms and potential roles in disease

2012 ◽  
Vol 24 (6) ◽  
pp. 736-739 ◽  
Author(s):  
Shida Yousefi ◽  
Dagmar Simon ◽  
Hans-Uwe Simon
Author(s):  
Marina Valente Barroso ◽  
Josiane Sabbadini Neves

2014 ◽  
Vol 192 (11) ◽  
pp. 5314-5323 ◽  
Author(s):  
Mahbubul Morshed ◽  
Ruslan Hlushchuk ◽  
Dagmar Simon ◽  
Andrew F. Walls ◽  
Kazushige Obata-Ninomiya ◽  
...  

2016 ◽  
Vol 60 (10) ◽  
pp. 5957-5967 ◽  
Author(s):  
Katrin Schilcher ◽  
Federica Andreoni ◽  
Vanina Dengler Haunreiter ◽  
Kati Seidl ◽  
Barbara Hasse ◽  
...  

ABSTRACTStaphylococcus aureusbiofilms are extremely difficult to treat. They provide a protected niche for the bacteria, rendering them highly recalcitrant toward host defenses as well as antibiotic treatment. Bacteria within a biofilm are shielded from the immune system by the formation of an extracellular polymeric matrix, composed of polysaccharides, extracellular DNA (eDNA), and proteins. Many antibiotics do not readily penetrate biofilms, resulting in the presence of subinhibitory concentrations of antibiotics. Here, we show that subinhibitory concentrations of clindamycin triggered a transcriptional stress response inS. aureusvia the alternative sigma factor B (σB) and upregulated the expression of the major biofilm-associated genesatlA,lrgA,agrA, thepsmgenes,fnbA, andfnbB. Our data suggest that subinhibitory concentrations of clindamycin alter the ability ofS. aureusto form biofilms and shift the composition of the biofilm matrix toward higher eDNA content. An understanding of the molecular mechanisms underlying biofilm assembly and dispersal in response to subinhibitory concentrations of clinically relevant antibiotics such as clindamycin is critical to further optimize antibiotic treatment strategies of biofilm-associatedS. aureusinfections.


Allergy ◽  
2014 ◽  
Vol 69 (12) ◽  
pp. 1696-1700 ◽  
Author(s):  
A. A. Cunha ◽  
B. N. Porto ◽  
N. K. Nuñez ◽  
R. G. Souza ◽  
M. H. M. Vargas ◽  
...  

2018 ◽  
Vol 141 (2) ◽  
pp. 571-585.e7 ◽  
Author(s):  
Valdirene S. Muniz ◽  
Juliana C. Silva ◽  
Yasmim A.V. Braga ◽  
Rossana C.N. Melo ◽  
Shigeharu Ueki ◽  
...  

2021 ◽  
Vol 2 ◽  
Author(s):  
Hannah J. Serrage ◽  
Mark A. Jepson ◽  
Nadia Rostami ◽  
Nicholas S. Jakubovics ◽  
Angela H. Nobbs

Dental plaque is the key etiological agent in caries formation and the development of the prevalent chronic oral inflammatory disease, periodontitis. The dental plaque biofilm comprises a diverse range of microbial species encased within a rich extracellular matrix, of which extracellular DNA (eDNA) has been identified as an important component. The molecular mechanisms of eDNA release and the structure of eDNA have yet to be fully characterized. Nonetheless, key functions that have been proposed for eDNA include maintaining biofilm structural integrity, initiating adhesion to dental surfaces, acting as a nutrient source, and facilitating horizontal gene transfer. Thus, eDNA is a potential therapeutic target for the management of oral disease–associated biofilm. This review aims to summarize advances in the understanding of the mechanisms of eDNA release from oral microorganisms and in the methods of eDNA detection and quantification within oral biofilms.


2021 ◽  
Vol 12 ◽  
Author(s):  
Edgar Ramos-Martínez ◽  
Leticia Hernández-González ◽  
Iván Ramos-Martínez ◽  
Laura Pérez-Campos Mayoral ◽  
Georgina I. López-Cortés ◽  
...  

Extracellular DNA traps (ETs) are evolutionarily conserved antimicrobial mechanisms present in protozoa, plants, and animals. In this review, we compare their similarities in species of different taxa, and put forward the hypothesis that ETs have multiple origins. Our results are consistent with a process of evolutionary convergence in multicellular organisms through the application of a congruency test. Furthermore, we discuss why multicellularity is related to the presence of a mechanism initiating the formation of ETs.


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