<i>Klebsiella pneumoniae C</i>o-infection Leads to Fatal Pneumonia in SARS-CoV-2-infected Mice
Abstract SARS-CoV-2 patients have been reported to have high rates of secondaryKlebsiella pneumoniaeinfections.Klebsiella pneumoniaeis a commensal that is typically found in the respiratory and gastrointestinal tracts. However, it can cause severe disease when a person’s immune system is compromised. Despite a high number ofK. pneumoniaecases reported in SARS-CoV-2 patients, a co-infection animal model evaluating the pathogenesis is not available. We describe a mouse model to study disease pathogenesis of SARS-CoV-2 andK. pneumoniaeco-infection. BALB/cJ mice were inoculated with mouse-adapted SARS-CoV-2 followed by a challenge withK. pneumoniae. Mice were monitored for body weight change, clinical signs, and survival during infection. The bacterial load, viral titers, immune cell accumulation and phenotype, and histopathology were evaluated in the lungs. The co-infected mice showed severe clinical disease and a higher mortality rate within 48 h ofK. pneumoniaeinfection. The co-infected mice had significantly elevated bacterial load in the lungs, however, viral loads were similar between co-infected and single-infected mice. Histopathology of co-infected mice showed severe bronchointerstitial pneumonia with copious intralesional bacteria. Flow cytometry analysis showed significantly higher numbers of neutrophils and macrophages in the lungs. Collectively, our results demonstrated that co-infection of SARS-CoV-2 withK. pneumoniaecauses severe disease with increased mortality in mice..
| Medienart: |
|
|---|
Preprint| Erscheinungsjahr: |
2023 |
|---|---|
| Erschienen: |
2023 |
| Enthalten in: |
bioRxiv.org - (2023) vom: 03. Aug. Zur Gesamtaufnahme - year:2023 |
|---|
| Sprache: |
Englisch |
|---|
| Beteiligte Personen: |
Villalva, Crystal [VerfasserIn] |
|---|
| Links: |
Volltext [kostenfrei] |
|---|
| Themen: |
|---|
| doi: |
10.1101/2023.07.28.551035 |
|---|
| funding: |
|
|---|---|
| Förderinstitution / Projekttitel: |
|
| PPN (Katalog-ID): |
XBI040402460 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | XBI040402460 | ||
| 003 | DE-627 | ||
| 005 | 20231205144513.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 230803s2023 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1101/2023.07.28.551035 |2 doi | |
| 035 | |a (DE-627)XBI040402460 | ||
| 035 | |a (biorXiv)10.1101/2023.07.28.551035 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 100 | 1 | |a Villalva, Crystal |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a <i>Klebsiella pneumoniae C</i>o-infection Leads to Fatal Pneumonia in SARS-CoV-2-infected Mice |
| 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 SARS-CoV-2 patients have been reported to have high rates of secondaryKlebsiella pneumoniaeinfections.Klebsiella pneumoniaeis a commensal that is typically found in the respiratory and gastrointestinal tracts. However, it can cause severe disease when a person’s immune system is compromised. Despite a high number ofK. pneumoniaecases reported in SARS-CoV-2 patients, a co-infection animal model evaluating the pathogenesis is not available. We describe a mouse model to study disease pathogenesis of SARS-CoV-2 andK. pneumoniaeco-infection. BALB/cJ mice were inoculated with mouse-adapted SARS-CoV-2 followed by a challenge withK. pneumoniae. Mice were monitored for body weight change, clinical signs, and survival during infection. The bacterial load, viral titers, immune cell accumulation and phenotype, and histopathology were evaluated in the lungs. The co-infected mice showed severe clinical disease and a higher mortality rate within 48 h ofK. pneumoniaeinfection. The co-infected mice had significantly elevated bacterial load in the lungs, however, viral loads were similar between co-infected and single-infected mice. Histopathology of co-infected mice showed severe bronchointerstitial pneumonia with copious intralesional bacteria. Flow cytometry analysis showed significantly higher numbers of neutrophils and macrophages in the lungs. Collectively, our results demonstrated that co-infection of SARS-CoV-2 withK. pneumoniaecauses severe disease with increased mortality in mice. | ||
| 650 | 4 | |a Biology |7 (dpeaa)DE-84 | |
| 650 | 4 | |a 570 |7 (dpeaa)DE-84 | |
| 700 | 1 | |a Patil, Girish |4 aut | |
| 700 | 1 | |a Narayanan, Sai |4 aut | |
| 700 | 1 | |a Chanda, Debarati |4 aut | |
| 700 | 1 | |a Ghimire, Roshan |4 aut | |
| 700 | 1 | |a Snider, Timothy |4 aut | |
| 700 | 1 | |a Ramachandran, Akhilesh |4 aut | |
| 700 | 1 | |a Channappanavar, Rudragouda |4 aut | |
| 700 | 1 | |a More, Sunil |0 (orcid)0000-0001-5007-8795 |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t bioRxiv.org |g (2023) vom: 03. Aug. |
| 773 | 1 | 8 | |g year:2023 |g day:03 |g month:08 |
| 856 | 4 | 0 | |u http://dx.doi.org/10.1101/2023.07.28.551035 |z kostenfrei |3 Volltext |
| 912 | |a GBV_XBI | ||
| 951 | |a AR | ||
| 952 | |j 2023 |b 03 |c 08 | ||