Gut microbiota from patients with mild COVID-19 cause alterations in mice that resemble post-COVID syndrome
Abstract Background There is mounting evidence that SARS-CoV-2 targets tissues beyond the respiratory tract. Long-term sequelae after COVID-19 are frequent and of major concern. Prolonged virus detection in the gut has been particularly intriguing. Of note, SARS-CoV-2 infection also disturbs the gut microbiota composition, a finding linked with disease severity in patients with COVID-19. Here, we aimed to characterize the functional role of the gut microbiota in the long-term consequences of COVID-19. To this end, we characterized the gut microbiota from COVID-19 human subjects and followed the effects of human fecal transfer to germ-free mice. Results The gut microbiota of post-COVID subjects (up to 4 months from the initial positive test) revealed a remarkable predominance of Enterobacteriaceae strains with multidrug-resistance phenotype compared to healthy controls. After fecal transfer to germ-free mice, animals receiving samples from post-COVID subjects displayed higher lung inflammation and increased susceptibility to pulmonary infection caused by an antimicrobial resistant Klebsiella pneumoniae strain. These mice also showed poorer cognitive performance associated with increased expression of TNF-α, reduced levels of brain-derived neurotrophic factor-BDNF and postsynaptic density protein-PSD-95 in the brain, as well as alterations of several biochemical pathways. These alterations were observed in the absence of SARS-CoV-2, suggesting that alterations in the gut microbiota caused them. Consistent with this hypothesis, brain dysfunctions induced in a mouse model of coronavirus infection were partially prevented by modulation of the microbiota via treatment with the commensal probiotic bacteria Bifidobacterium longum 51A. Conclusions Our results show prolonged impact of SARS-CoV-2 infection in the gut microbiota that persists even after the individuals have cleared the virus. Increased Enterobacteriaceae with antimicrobial resistance phenotype were of particular concern. Moreover, microbiota transfer from post-COVID subjects induced loss of brain cognitive functions and impaired lung defense in mice. Altogether, our work emphasizes the importance of microbiota as a target for therapies to help treat post-COVID sequelae..
| Medienart: |
|
|---|
Preprint| Erscheinungsjahr: |
2023 |
|---|---|
| Erschienen: |
2023 |
| Enthalten in: |
ResearchSquare.com - (2023) vom: 12. Apr. Zur Gesamtaufnahme - year:2023 |
|---|
| Sprache: |
Englisch |
|---|
| Links: |
Volltext [kostenfrei] |
|---|
| Themen: |
|---|
| doi: |
10.21203/rs.3.rs-1756189/v1 |
|---|
| funding: |
|
|---|---|
| Förderinstitution / Projekttitel: |
|
| PPN (Katalog-ID): |
XRA036340081 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | XRA036340081 | ||
| 003 | DE-627 | ||
| 005 | 20230429175609.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 220623s2023 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.21203/rs.3.rs-1756189/v1 |2 doi | |
| 035 | |a (DE-627)XRA036340081 | ||
| 035 | |a (ResearchSquare)10.21203/rs.3.rs-1756189/v1 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 100 | 1 | |a de Almeida, Viviani Mendes |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Gut microbiota from patients with mild COVID-19 cause alterations in mice that resemble post-COVID syndrome |
| 264 | 1 | |c 2023 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
| 338 | |a Online-Ressource |b cr |2 rdacarrier | ||
| 520 | |a Abstract Background There is mounting evidence that SARS-CoV-2 targets tissues beyond the respiratory tract. Long-term sequelae after COVID-19 are frequent and of major concern. Prolonged virus detection in the gut has been particularly intriguing. Of note, SARS-CoV-2 infection also disturbs the gut microbiota composition, a finding linked with disease severity in patients with COVID-19. Here, we aimed to characterize the functional role of the gut microbiota in the long-term consequences of COVID-19. To this end, we characterized the gut microbiota from COVID-19 human subjects and followed the effects of human fecal transfer to germ-free mice. Results The gut microbiota of post-COVID subjects (up to 4 months from the initial positive test) revealed a remarkable predominance of Enterobacteriaceae strains with multidrug-resistance phenotype compared to healthy controls. After fecal transfer to germ-free mice, animals receiving samples from post-COVID subjects displayed higher lung inflammation and increased susceptibility to pulmonary infection caused by an antimicrobial resistant Klebsiella pneumoniae strain. These mice also showed poorer cognitive performance associated with increased expression of TNF-α, reduced levels of brain-derived neurotrophic factor-BDNF and postsynaptic density protein-PSD-95 in the brain, as well as alterations of several biochemical pathways. These alterations were observed in the absence of SARS-CoV-2, suggesting that alterations in the gut microbiota caused them. Consistent with this hypothesis, brain dysfunctions induced in a mouse model of coronavirus infection were partially prevented by modulation of the microbiota via treatment with the commensal probiotic bacteria Bifidobacterium longum 51A. Conclusions Our results show prolonged impact of SARS-CoV-2 infection in the gut microbiota that persists even after the individuals have cleared the virus. Increased Enterobacteriaceae with antimicrobial resistance phenotype were of particular concern. Moreover, microbiota transfer from post-COVID subjects induced loss of brain cognitive functions and impaired lung defense in mice. Altogether, our work emphasizes the importance of microbiota as a target for therapies to help treat post-COVID sequelae. | ||
| 650 | 4 | |a Biology |7 (dpeaa)DE-84 | |
| 650 | 4 | |a 570 |7 (dpeaa)DE-84 | |
| 700 | 1 | |a Engel, Daiane F |4 aut | |
| 700 | 1 | |a Ricci, Mayra Fernanda |4 aut | |
| 700 | 1 | |a Cruz, Clênio Silva |4 aut | |
| 700 | 1 | |a Lopes, Icaro Santos |4 aut | |
| 700 | 1 | |a Alves, Daniele Almeida |4 aut | |
| 700 | 1 | |a Auriol, Mirna d’ |4 aut | |
| 700 | 1 | |a Magalhães, João |4 aut | |
| 700 | 1 | |a Zuccoli, Giuliana S. |4 aut | |
| 700 | 1 | |a Smith, Bradley Joseph |4 aut | |
| 700 | 1 | |a Carregari, Victor Corasolla |4 aut | |
| 700 | 1 | |a Machado, Elayne Cristina |4 aut | |
| 700 | 1 | |a Rocha, Victor M. |4 aut | |
| 700 | 1 | |a Carvalho, Toniana G. |4 aut | |
| 700 | 1 | |a Lacerda, Larisse de Souza Barbosa |4 aut | |
| 700 | 1 | |a Pimenta, Jordane C. |4 aut | |
| 700 | 1 | |a Galvão, Izabela |4 aut | |
| 700 | 1 | |a Silva, Mariana Aganetti |4 aut | |
| 700 | 1 | |a Rosa, Erika da Silva |4 aut | |
| 700 | 1 | |a Cassali, Geovanni Dantas |4 aut | |
| 700 | 1 | |a Garcia, Cristiana C. |4 aut | |
| 700 | 1 | |a Teixeira, Mauro Martins |4 aut | |
| 700 | 1 | |a Coelho, Leiliane |4 aut | |
| 700 | 1 | |a Ribeiro, Fabiola Mara |4 aut | |
| 700 | 1 | |a Martins, Flaviano S. |4 aut | |
| 700 | 1 | |a Saia, Rafael Simone |4 aut | |
| 700 | 1 | |a Costa, Vivian Vasconcelos |4 aut | |
| 700 | 1 | |a Martins-de-Souza, Daniel |4 aut | |
| 700 | 1 | |a Marques, João T. |4 aut | |
| 700 | 1 | |a Aguiar, Eric R. G. R. |4 aut | |
| 700 | 1 | |a Vieira, Angelica T. |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t ResearchSquare.com |g (2023) vom: 12. Apr. |
| 773 | 1 | 8 | |g year:2023 |g day:12 |g month:04 |
| 856 | 4 | 0 | |u http://dx.doi.org/10.21203/rs.3.rs-1756189/v1 |z kostenfrei |3 Volltext |
| 912 | |a GBV_XRA | ||
| 912 | |a SSG-OLC-PHA | ||
| 951 | |a AR | ||
| 952 | |j 2023 |b 12 |c 04 | ||