TY - JOUR
T1 - Reactive Persulfides from Salmonella Typhimurium Downregulate Autophagy-Mediated Innate Immunity in Macrophages by Inhibiting Electrophilic Signaling
AU - Khan, Shahzada
AU - Fujii, Shigemoto
AU - Matsunaga, Tetsuro
AU - Nishimura, Akira
AU - Ono, Katsuhiko
AU - Ida, Tomoaki
AU - Ahmed, Khandaker Ahtesham
AU - Okamoto, Tatsuya
AU - Tsutsuki, Hiroyasu
AU - Sawa, Tomohiro
AU - Akaike, Takaaki
N1 - Funding Information:
We thank Judith B. Gandy for her excellent editing of the manuscript. Thanks are also due to M.H.A. Rahman and Soichiro Akashi for their technical assistance. This work was supported in part by Grants-in-Aid for Scientific Research ( 25253020 , 26670207 , and 16K15208 to T.A.; 24590527 and 15K08456 to S.F.) and a Grant-in-Aid for Scientific Research on Innovative Areas ( 26111008 to T.A.) from the Ministry of Education, Sciences, Sports and Technology (MEXT), Japan.
Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2018/11/15
Y1 - 2018/11/15
N2 - Reactive persulfides such as cysteine persulfide and glutathione persulfide are produced by bacteria including Salmonella during sulfur metabolism. The biological significance of bacterial reactive persulfides in host-pathogen interactions still warrants investigation. We found that reactive persulfides produced by Salmonella Typhimurium LT2 regulate macrophage autophagy via metabolizing 8-nitroguanosine 3′,5′-cyclic monophosphate (8-nitro-cGMP), an electrophilic product of reactive oxygen species and nitric oxide signaling. 8-Nitro-cGMP signaling was required for efficient autophagy-mediated clearance of Salmonella from infected macrophages. In the infected cells, 8-nitro-cGMP caused cGMP adduct formation (S-guanylation) of bacterial surface proteins, which triggered recruitment of autophagy-related proteins p62 and LC3-II to the intracellular bacteria. We also found that Salmonella-produced reactive persulfides downregulated this autophagy by decreasing cellular 8-nitro-cGMP content, thereby inhibiting electrophilic signaling. These data reveal a pathogenic role of bacteria-derived reactive persulfides via suppression of anti-bacterial autophagy. Khan et al. found that reactive persulfides produced by Salmonella inhibit autophagy-mediated bacterial clearance by regulating electrophilic signaling. These data reveal a pathogenic role of bacteria-derived reactive persulfides via suppression of anti-bacterial autophagy.
AB - Reactive persulfides such as cysteine persulfide and glutathione persulfide are produced by bacteria including Salmonella during sulfur metabolism. The biological significance of bacterial reactive persulfides in host-pathogen interactions still warrants investigation. We found that reactive persulfides produced by Salmonella Typhimurium LT2 regulate macrophage autophagy via metabolizing 8-nitroguanosine 3′,5′-cyclic monophosphate (8-nitro-cGMP), an electrophilic product of reactive oxygen species and nitric oxide signaling. 8-Nitro-cGMP signaling was required for efficient autophagy-mediated clearance of Salmonella from infected macrophages. In the infected cells, 8-nitro-cGMP caused cGMP adduct formation (S-guanylation) of bacterial surface proteins, which triggered recruitment of autophagy-related proteins p62 and LC3-II to the intracellular bacteria. We also found that Salmonella-produced reactive persulfides downregulated this autophagy by decreasing cellular 8-nitro-cGMP content, thereby inhibiting electrophilic signaling. These data reveal a pathogenic role of bacteria-derived reactive persulfides via suppression of anti-bacterial autophagy. Khan et al. found that reactive persulfides produced by Salmonella inhibit autophagy-mediated bacterial clearance by regulating electrophilic signaling. These data reveal a pathogenic role of bacteria-derived reactive persulfides via suppression of anti-bacterial autophagy.
KW - 8-nitroguanosine 3′,5′-cyclic monophosphate
KW - autophagy
KW - electrophilic signaling
KW - host-pathogen interaction
KW - reactive persulfides
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U2 - 10.1016/j.chembiol.2018.08.007
DO - 10.1016/j.chembiol.2018.08.007
M3 - Article
C2 - 30197193
AN - SCOPUS:85056565193
SN - 2451-9448
VL - 25
SP - 1403-1413.e4
JO - Cell Chemical Biology
JF - Cell Chemical Biology
IS - 11
ER -