tetano
Editor, Senior Moderator
J Transl Med
. 2024 Nov 21;22(1):1049.
doi: 10.1186/s12967-024-05879-0. Maternal infection of SARS-CoV-2 during the first and second trimesters leads to newborn telomere shortening
Lina Wang[SUP] #[/SUP][SUP] 1 [/SUP], Junfeng Zhang[SUP] #[/SUP][SUP] 2 [/SUP], Fangfei Liu[SUP] 1 [/SUP], Qixiang Shi[SUP] 3 [/SUP], Fengchun Gao[SUP] 2 [/SUP], Junmin Li[SUP] 2 [/SUP], Yanhua Liu[SUP] 2 [/SUP], Feng Kong[SUP] 4 5 [/SUP], Dawei Xu[SUP] 6 [/SUP]
Affiliations
Background: Initial telomere length (TL) in newborns is the major determinant for TL in later life while TL in newborn/early-life predicts long-term health and lifespan. It is important to identify key factors that affect telomere homeostasis throughout embryonic development for precision interventions to maintain optimal TL in fetus/prenatal infants. SARS-CoV-2 has caused a widespread global pandemic of COVID-19, but it remains unclear whether maternal SARS-CoV-2 infection impairs prenatal telomere homeostasis.
Methods: We recruited 413 normally delivered newborns whose mothers were either non-infected or infected with SARS-CoV-2 during different trimesters of pregnancy (otherwise healthy). Telomere length (TL) in cord blood (CB) was assessed using qPCR. CB and maternal blood were analyzed for cytokine levels. Placental senescence was determined using senescence-associated β-galactosidase staining.
Results: Control (non-infected maternal) newborn TL was significantly longer than that from maternal infection (1.568 ± 0.340 vs 1.390 ± 0.350, P = 0.005). Such shorter TL was observed only if maternal infection of SARS-CoV-2 occurred in the first and second trimesters of pregnancy (1.261 ± 0.340 and 1.346 ± 0.353, P < 0.0001 and 0.001, respectively). There were no differences in TL between controls and infection at the third trimester (1.568 ± 0.340 vs 1.565 ± 0.329, P > 0.05). Across the first trimester, there was a positive correlation between newborn TL and gestational weeks with maternal infection, suggesting that the earlier maternal infection occurs, the worse effect is taken on fetal telomere homeostasis. Placental senescence coupled with the downregulated expression of telomerase reverse transcriptase was significantly more frequent from the maternal infection at the first trimester. There were no differences in IL-6, C reactive protein and other cytokine levels in CB and maternal serum or placentas.
Conclusions: Maternal SARS-CoV-2 infection at the first and second trimesters leads to significantly shorter TL and earlier infection causes much more severe TL damage. The infection-mediated cell senescence and other histopathological abnormalities result in defective placental function through which fetal telomere homeostasis is impaired. Thus, vaccination against COVID-19 should be done in advance for women who plan pregnancy.
Keywords: Maternal infection; Newborns; Placental senescence; SARS-CoV-2; Telomere length.
. 2024 Nov 21;22(1):1049.
doi: 10.1186/s12967-024-05879-0. Maternal infection of SARS-CoV-2 during the first and second trimesters leads to newborn telomere shortening
Lina Wang[SUP] #[/SUP][SUP] 1 [/SUP], Junfeng Zhang[SUP] #[/SUP][SUP] 2 [/SUP], Fangfei Liu[SUP] 1 [/SUP], Qixiang Shi[SUP] 3 [/SUP], Fengchun Gao[SUP] 2 [/SUP], Junmin Li[SUP] 2 [/SUP], Yanhua Liu[SUP] 2 [/SUP], Feng Kong[SUP] 4 5 [/SUP], Dawei Xu[SUP] 6 [/SUP]
Affiliations
- PMID: 39574146
- PMCID: PMC11580642
- DOI: 10.1186/s12967-024-05879-0
Background: Initial telomere length (TL) in newborns is the major determinant for TL in later life while TL in newborn/early-life predicts long-term health and lifespan. It is important to identify key factors that affect telomere homeostasis throughout embryonic development for precision interventions to maintain optimal TL in fetus/prenatal infants. SARS-CoV-2 has caused a widespread global pandemic of COVID-19, but it remains unclear whether maternal SARS-CoV-2 infection impairs prenatal telomere homeostasis.
Methods: We recruited 413 normally delivered newborns whose mothers were either non-infected or infected with SARS-CoV-2 during different trimesters of pregnancy (otherwise healthy). Telomere length (TL) in cord blood (CB) was assessed using qPCR. CB and maternal blood were analyzed for cytokine levels. Placental senescence was determined using senescence-associated β-galactosidase staining.
Results: Control (non-infected maternal) newborn TL was significantly longer than that from maternal infection (1.568 ± 0.340 vs 1.390 ± 0.350, P = 0.005). Such shorter TL was observed only if maternal infection of SARS-CoV-2 occurred in the first and second trimesters of pregnancy (1.261 ± 0.340 and 1.346 ± 0.353, P < 0.0001 and 0.001, respectively). There were no differences in TL between controls and infection at the third trimester (1.568 ± 0.340 vs 1.565 ± 0.329, P > 0.05). Across the first trimester, there was a positive correlation between newborn TL and gestational weeks with maternal infection, suggesting that the earlier maternal infection occurs, the worse effect is taken on fetal telomere homeostasis. Placental senescence coupled with the downregulated expression of telomerase reverse transcriptase was significantly more frequent from the maternal infection at the first trimester. There were no differences in IL-6, C reactive protein and other cytokine levels in CB and maternal serum or placentas.
Conclusions: Maternal SARS-CoV-2 infection at the first and second trimesters leads to significantly shorter TL and earlier infection causes much more severe TL damage. The infection-mediated cell senescence and other histopathological abnormalities result in defective placental function through which fetal telomere homeostasis is impaired. Thus, vaccination against COVID-19 should be done in advance for women who plan pregnancy.
Keywords: Maternal infection; Newborns; Placental senescence; SARS-CoV-2; Telomere length.