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bioRxiv · 10.1101/2022.11.11.515814

The chemorepellent, SLIT2, bolsters innate immunity against Staphylococcus aureus

Abstract

Neutrophils are essential for host defense against Staphylococcus aureus (S. aureus). The neuro-repellent, SLIT2, potently inhibits neutrophil chemotaxis, and might therefore be expected to impair antibacterial responses. We report here that, unexpectedly, neutrophils exposed to the N-terminal SLIT2 (N-SLIT2) fragment kill extracellular S. aureus more efficiently. N-SLIT2 amplifies reactive oxygen species production in response to the bacteria by activating p38 mitogen-activated protein kinase that in turn phosphorylates NCF1, an essential subunit of the NADPH oxidase complex. N-SLIT2 also enhances exocytosis of secondary granules. In a murine model of S. aureus skin and soft tissue infection (SSTI), local SLIT2 levels fall initially but increase subsequently, peaking {approx} 3 days after infection. Of note, neutralization of endogenous SLIT2 worsens SSTI. Temporal fluctuations in tissue SLIT2 levels may promote neutrophil recruitment and retention at the infection site and hasten bacterial clearance by augmenting neutrophil oxidative burst and degranulation. Collectively, these actions of SLIT2 coordinate innate immune responses to limit susceptibility to S. aureus. One-sentence summarySLIT2, a prototypic neuro-repellent, spatiotemporally coordinates host defense against Staphylococcus aureus infection.

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BibTeXRIS

Bhosle, V. K., Sun, C., Patel, S., Westman, J., Ammendolia, D. A., Fine, N., Li, Z., Sharma, M., Glogauer, J., Capurro, M. I., Jones, N. L., Glogauer, M., Grinstein, S., Robinson, L. A.. 2022-11-12. The chemorepellent, SLIT2, bolsters innate immunity against Staphylococcus aureus. https://doi.org/10.1101/2022.11.11.515814

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