tetano
Editor, Senior Moderator
Aging Cell
. 2022 Oct 18;e13729.
doi: 10.1111/acel.13729. Online ahead of print.
DNA damage contributes to age-associated differences in SARS-CoV-2 infection
Rui Jin[SUP] 1 [/SUP], Chang Niu[SUP] 2 [/SUP], Fengyun Wu[SUP] 2 [/SUP], Sixin Zhou[SUP] 3 [/SUP], Tao Han[SUP] 4 [/SUP], Zhe Zhang[SUP] 1 [/SUP], Entao Li[SUP] 5 [/SUP], Xiaona Zhang[SUP] 2 [/SUP], Shanrong Xu[SUP] 6 [/SUP], Jiadong Wang[SUP] 7 [/SUP], Shen Tian[SUP] 2 [/SUP], Wei Chen[SUP] 1 [/SUP], Qinong Ye[SUP] 1 [/SUP], Cheng Cao[SUP] 1 [/SUP], Long Cheng[SUP] 1 [/SUP]
Affiliations
Abstract
Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is known to disproportionately affect older individuals. How aging processes affect SARS-CoV-2 infection and disease progression remains largely unknown. Here, we found that DNA damage, one of the hallmarks of aging, promoted SARS-CoV-2 infection in vitro and in vivo. SARS-CoV-2 entry was facilitated by DNA damage caused by extrinsic genotoxic stress or telomere dysfunction and hampered by inhibition of the DNA damage response (DDR). Mechanistic analysis revealed that DDR increased expression of angiotensin-converting enzyme 2 (ACE2), the primary receptor of SARS-CoV-2, by activation of transcription factor c-Jun. Importantly, in vivo experiment using a mouse-adapted viral strain also verified the significant roles of DNA damage in viral entry and severity of infection. Expression of ACE2 was elevated in the older human and mice tissues and positively correlated with γH2AX, a DNA damage biomarker, and phosphorylated c-Jun (p-c-Jun). Finally, nicotinamide mononucleotide (NMN) and MDL-800, which promote DNA repair, alleviated SARS-CoV-2 infection and disease severity in vitro and in vivo. Taken together, our data provide insights into the age-associated differences in SARS-CoV-2 infection and a novel approach for antiviral intervention.
Keywords: DNA damage; aging; telomere; viral infection.
. 2022 Oct 18;e13729.
doi: 10.1111/acel.13729. Online ahead of print.
DNA damage contributes to age-associated differences in SARS-CoV-2 infection
Rui Jin[SUP] 1 [/SUP], Chang Niu[SUP] 2 [/SUP], Fengyun Wu[SUP] 2 [/SUP], Sixin Zhou[SUP] 3 [/SUP], Tao Han[SUP] 4 [/SUP], Zhe Zhang[SUP] 1 [/SUP], Entao Li[SUP] 5 [/SUP], Xiaona Zhang[SUP] 2 [/SUP], Shanrong Xu[SUP] 6 [/SUP], Jiadong Wang[SUP] 7 [/SUP], Shen Tian[SUP] 2 [/SUP], Wei Chen[SUP] 1 [/SUP], Qinong Ye[SUP] 1 [/SUP], Cheng Cao[SUP] 1 [/SUP], Long Cheng[SUP] 1 [/SUP]
Affiliations
- PMID: 36254583
- DOI: 10.1111/acel.13729
Abstract
Coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is known to disproportionately affect older individuals. How aging processes affect SARS-CoV-2 infection and disease progression remains largely unknown. Here, we found that DNA damage, one of the hallmarks of aging, promoted SARS-CoV-2 infection in vitro and in vivo. SARS-CoV-2 entry was facilitated by DNA damage caused by extrinsic genotoxic stress or telomere dysfunction and hampered by inhibition of the DNA damage response (DDR). Mechanistic analysis revealed that DDR increased expression of angiotensin-converting enzyme 2 (ACE2), the primary receptor of SARS-CoV-2, by activation of transcription factor c-Jun. Importantly, in vivo experiment using a mouse-adapted viral strain also verified the significant roles of DNA damage in viral entry and severity of infection. Expression of ACE2 was elevated in the older human and mice tissues and positively correlated with γH2AX, a DNA damage biomarker, and phosphorylated c-Jun (p-c-Jun). Finally, nicotinamide mononucleotide (NMN) and MDL-800, which promote DNA repair, alleviated SARS-CoV-2 infection and disease severity in vitro and in vivo. Taken together, our data provide insights into the age-associated differences in SARS-CoV-2 infection and a novel approach for antiviral intervention.
Keywords: DNA damage; aging; telomere; viral infection.