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. 2021 Jul 28;22(15):8046. doi: 10.3390/ijms22158046

Table 1.

Summary of mechanisms of neutrophil extracellular trap formation in different species.

Microorganisms Species Mechanism Types of NETosis References
BACTERIA
Staphylococcus aureus Mice
Humans
Bovine
Dependent on TLR2 and Complement C3 in mice PAD4 dependent
Response to virulence factor, PVL in a ROS independent manner
DNA extruded via vesicles
Unknown
Vital
Vital
Unknown
[26]
[40]
[27]
E. coli Humans *
Mice *
Bovine
* Mediated via platelet TLR4
Histone H3 citrullination by PAD4
Vital in the
presence of
platelets
[39]
[28]
E. coli LPS Humans * * Mediated via platelet TLR4 and present HMGB1 to neutrophils Vital in vivo [29]
VIRUS
Influenza A
Influenza H1N1
Mice
Humans
Not dependent on PAD4
ROS and PAD4 dependent
Suicidal
Suicidal
[30]
PARASITES
Eimeria bovis Bovine Recognition by CD11b
Dependent on NAPDH oxidase, NE and MPO Requires p38 MAPK and ERK1/2 phosphorylation
Unknown [31]
[32]
Eimeria arloingi Goat NADPH oxidase dependent Unknown [33]
Besnoitia besnoiti Bovine Dependent on NAPDH oxidase, NE and MPO Unknown [34]
Toxoplasma gondii Humans
Mice
ERK-MEK dependent
* NADPH oxidase/ROS dependent
Suicidal [35]

TLR, toll-like receptor; C3, complement 3; PAD4, peptidyl arginine deiminase 4; PVL, Panto-Valentine leukocidin; HMGB1, high mobility group box 1; ROS, reactive oxygen species; NE, neutrophil elastase; MPO, myeloperoxidase; MAPK, mitogen-activated protein kinase, ERK1/2; extracellular signal regulated kinase ½, NADPH; nicotinamide adenine dinucleotide phosphate. * Mechanism found in specified species.