Gut microbiota from patients with COVID-19 cause alterations in mice that resemble post-COVID symptoms.
Mendes de Almeida, V
Engel, DF
Ricci, MF
Cruz, CS
Lopes, ÍS
Alves, DA
d' Auriol, M
Magalhães, J
Machado, EC
Rocha, VM
Carvalho, TG
Lacerda, LSB
Pimenta, JC
Aganetti, M
Zuccoli, GS
Smith, BJ
Carregari, VC
da Silva Rosa, E
Galvão, I
Dantas Cassali, G
Garcia, CC
Teixeira, MM
André, LC
Ribeiro, FM
Martins, FS
Saia, RS
Costa, VV
Martins-de-Souza, D
Hansbro, PM
Marques, JT
Aguiar, ERGR
Vieira, AT
- Publisher:
- Taylor & Francis
- Publication Type:
- Journal Article
- Citation:
- Gut Microbes, 2023, 15, (2), pp. 2249146
- Issue Date:
- 2023-12
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Mendes de Almeida, V | |
dc.contributor.author | Engel, DF | |
dc.contributor.author | Ricci, MF | |
dc.contributor.author | Cruz, CS | |
dc.contributor.author | Lopes, ÍS | |
dc.contributor.author | Alves, DA | |
dc.contributor.author | d' Auriol, M | |
dc.contributor.author | Magalhães, J | |
dc.contributor.author | Machado, EC | |
dc.contributor.author | Rocha, VM | |
dc.contributor.author | Carvalho, TG | |
dc.contributor.author | Lacerda, LSB | |
dc.contributor.author | Pimenta, JC | |
dc.contributor.author | Aganetti, M | |
dc.contributor.author | Zuccoli, GS | |
dc.contributor.author | Smith, BJ | |
dc.contributor.author | Carregari, VC | |
dc.contributor.author | da Silva Rosa, E | |
dc.contributor.author | Galvão, I | |
dc.contributor.author | Dantas Cassali, G | |
dc.contributor.author | Garcia, CC | |
dc.contributor.author | Teixeira, MM | |
dc.contributor.author | André, LC | |
dc.contributor.author | Ribeiro, FM | |
dc.contributor.author | Martins, FS | |
dc.contributor.author | Saia, RS | |
dc.contributor.author | Costa, VV | |
dc.contributor.author | Martins-de-Souza, D | |
dc.contributor.author | Hansbro, PM | |
dc.contributor.author | Marques, JT | |
dc.contributor.author | Aguiar, ERGR | |
dc.contributor.author | Vieira, AT | |
dc.date.accessioned | 2023-09-20T00:25:49Z | |
dc.date.available | 2023-09-20T00:25:49Z | |
dc.date.issued | 2023-12 | |
dc.identifier.citation | Gut Microbes, 2023, 15, (2), pp. 2249146 | |
dc.identifier.issn | 1949-0976 | |
dc.identifier.issn | 1949-0984 | |
dc.identifier.uri | http://hdl.handle.net/10453/172205 | |
dc.description.abstract | Long-term sequelae of coronavirus disease (COVID)-19 are frequent and of major concern. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection affects the host gut microbiota, which is linked to disease severity in patients with COVID-19. Here, we report that the gut microbiota of post-COVID subjects had a remarkable predominance of Enterobacteriaceae strains with an antibiotic-resistant phenotype compared to healthy controls. Additionally, short-chain fatty acid (SCFA) levels were reduced in feces. Fecal transplantation from post-COVID subjects to germ-free mice led to lung inflammation and worse outcomes during pulmonary infection by multidrug-resistant Klebsiella pneumoniae. transplanted mice also exhibited poor cognitive performance. Overall, we show prolonged impacts of SARS-CoV-2 infection on the gut microbiota that persist after subjects have cleared the virus. Together, these data demonstrate that the gut microbiota can directly contribute to post-COVID sequelae, suggesting that it may be a potential therapeutic target. | |
dc.format | ||
dc.language | eng | |
dc.publisher | Taylor & Francis | |
dc.relation | http://purl.org/au-research/grants/nhmrc/1175134 | |
dc.relation | http://purl.org/au-research/grants/nhmrc/2010287 | |
dc.relation | http://purl.org/au-research/grants/nhmrc/GNT1175134 | |
dc.relation | http://purl.org/au-research/grants/nhmrc/GNT2010287 | |
dc.relation.ispartof | Gut Microbes | |
dc.relation.isbasedon | 10.1080/19490976.2023.2249146 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 0605 Microbiology | |
dc.subject.classification | 3107 Microbiology | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Mice | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Gastrointestinal Microbiome | |
dc.subject.mesh | SARS-CoV-2 | |
dc.subject.mesh | Anti-Bacterial Agents | |
dc.subject.mesh | Disease Progression | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Disease Progression | |
dc.subject.mesh | Anti-Bacterial Agents | |
dc.subject.mesh | Gastrointestinal Microbiome | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | SARS-CoV-2 | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Mice | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Gastrointestinal Microbiome | |
dc.subject.mesh | SARS-CoV-2 | |
dc.subject.mesh | Anti-Bacterial Agents | |
dc.subject.mesh | Disease Progression | |
dc.title | Gut microbiota from patients with COVID-19 cause alterations in mice that resemble post-COVID symptoms. | |
dc.type | Journal Article | |
utslib.citation.volume | 15 | |
utslib.location.activity | United States | |
utslib.for | 0605 Microbiology | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science/School of Life Sciences | |
pubs.organisational-group | /University of Technology Sydney/Strength - CFI - Centre for Inflammation | |
utslib.copyright.status | open_access | * |
dc.date.updated | 2023-09-20T00:25:38Z | |
pubs.issue | 2 | |
pubs.publication-status | Published | |
pubs.volume | 15 | |
utslib.citation.issue | 2 |
Abstract:
Long-term sequelae of coronavirus disease (COVID)-19 are frequent and of major concern. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection affects the host gut microbiota, which is linked to disease severity in patients with COVID-19. Here, we report that the gut microbiota of post-COVID subjects had a remarkable predominance of Enterobacteriaceae strains with an antibiotic-resistant phenotype compared to healthy controls. Additionally, short-chain fatty acid (SCFA) levels were reduced in feces. Fecal transplantation from post-COVID subjects to germ-free mice led to lung inflammation and worse outcomes during pulmonary infection by multidrug-resistant Klebsiella pneumoniae. transplanted mice also exhibited poor cognitive performance. Overall, we show prolonged impacts of SARS-CoV-2 infection on the gut microbiota that persist after subjects have cleared the virus. Together, these data demonstrate that the gut microbiota can directly contribute to post-COVID sequelae, suggesting that it may be a potential therapeutic target.
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