Accesso libero

Histopathological Analysis of Acinetobacter baumannii Lung Infection in a Mouse Model

SHIGERU TANSHO-NAGAKAWA

SHIGERU TANSHO-NAGAKAWA

Department of Microbiology and Immunology, Teikyo University School of MedicineTokyo, Japan
Profilo Orcid
Cerca questo autore su
Sciendo|Google Scholar
TANSHO-NAGAKAWA, SHIGERU
, 
YOSHINORI SATO

YOSHINORI SATO

Department of Microbiology and Immunology, Teikyo University School of MedicineTokyo, Japan
Cerca questo autore su
Sciendo|Google Scholar
SATO, YOSHINORI
, 
TSUNEYUKI UBAGAI

TSUNEYUKI UBAGAI

Department of Microbiology and Immunology, Teikyo University School of MedicineTokyo, Japan
Cerca questo autore su
Sciendo|Google Scholar
UBAGAI, TSUNEYUKI
, 
TAKANE KIKUCHI-UEDA

TAKANE KIKUCHI-UEDA

Department of Microbiology and Immunology, Teikyo University School of MedicineTokyo, Japan
Cerca questo autore su
Sciendo|Google Scholar
KIKUCHI-UEDA, TAKANE
, 
GO KAMOSHIDA

GO KAMOSHIDA

Department of Microbiology and Immunology, Teikyo University School of MedicineTokyo, Japan
Cerca questo autore su
Sciendo|Google Scholar
KAMOSHIDA, GO
, 
SATOSHI NISHIDA

SATOSHI NISHIDA

Department of Microbiology and Immunology, Teikyo University School of MedicineTokyo, Japan
Cerca questo autore su
Sciendo|Google Scholar
NISHIDA, SATOSHI
 e 
YASUO ONO

YASUO ONO

Department of Microbiology and Immunology, Teikyo University School of MedicineTokyo, Japan
Cerca questo autore su
Sciendo|Google Scholar
ONO, YASUO
  
20 dic 2021
Histopathological Analysis of Acinetobacter baumannii Lung Infection in a Mouse Model's Cover Image
INFORMAZIONI SU QUESTO ARTICOLO
Articolo precedente
Articolo Successivo
Cita
Scarica la copertina
Categoria dell'articolo: original-paper
Pubblicato online: 20 dic 2021
Pagine: 469 - 477
Ricevuto: 25 ago 2021
Accettato: 31 ott 2021
DOI: https://doi.org/10.33073/pjm-2021-044
Parole chiave
© 2021 Shigeru Tansho-Nagakawa et al., published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
undefined

Fig. 1.

Survival rates of mice with a lung infection. Survival rates of CH3/He mice following intratracheal inoculation with ATCC 19606 (A), TK1090 (B), and PAO-1 (C) strains. Groups of mice (ATCC 19606, TK1090, and PAO-1; n = 7 or 8 for uninfected and infected mice, respectively) were intratracheally inoculated as indicated, and their clinical outcome was monitored daily for up to 14 days.
Survival rates of mice with a lung infection. Survival rates of CH3/He mice following intratracheal inoculation with ATCC 19606 (A), TK1090 (B), and PAO-1 (C) strains. Groups of mice (ATCC 19606, TK1090, and PAO-1; n = 7 or 8 for uninfected and infected mice, respectively) were intratracheally inoculated as indicated, and their clinical outcome was monitored daily for up to 14 days.

Fig. 2.

Bacterial densities in mice infected with Acinetobacter baumannii. A. baumannii bacterial load in the lungs and kidneys of female C3H/HeN mice (groups of 3 mice for ATCC 19606- and TK1090-infected mice, respectively) intratracheally inoculated with 107 CFU of ATCC 19606 (open) and TK109 (closed) strains. Bacterial load in the respective organs was determined by quantitative bacteriology at 1 day (A) and 14 days (B) post-infection. The data are presented as the mean + standard deviation (SD). The detection limits for bacterial load were 1.3 log10 CFU/organ for the lung and kidney. Asterisks indicate statistically significant differences in the number of bacteria (*p < 0.05; ATCC 19606 vs. TK1090; unpaired t-test).
Bacterial densities in mice infected with Acinetobacter baumannii. A. baumannii bacterial load in the lungs and kidneys of female C3H/HeN mice (groups of 3 mice for ATCC 19606- and TK1090-infected mice, respectively) intratracheally inoculated with 107 CFU of ATCC 19606 (open) and TK109 (closed) strains. Bacterial load in the respective organs was determined by quantitative bacteriology at 1 day (A) and 14 days (B) post-infection. The data are presented as the mean + standard deviation (SD). The detection limits for bacterial load were 1.3 log10 CFU/organ for the lung and kidney. Asterisks indicate statistically significant differences in the number of bacteria (*p < 0.05; ATCC 19606 vs. TK1090; unpaired t-test).

Fig. 3.

Histopathological analysis of the lung tissues from Acinetobacter baumannii- and Pseudomonas aeruginosa-infected mice. The lung tissues from C3H/HeN mice infected with ATCC 19606 (A, B, C, and D), TK1090 (E, F, G, and H), and PAO-1 (I, J, K, and L) strains and uninfected mouse (M) are shown. The lung tissues from the mice infected with ATCC 19606 at 1 day (A), 2 days (B), 5 days (C), and 14 days (D) post-infection. The lung tissues from the mice infected with TK1090 at 1 day (E), 2 days (F), 5 days (G), and 14 days (H) post-infection. The lung tissues from the mice infected with PAO-1 at 1 day (I), 2 days (J), 5 days (K), and 14 days (L) post-infection. Photomicrograph images (magnification, 100×; hematoxylin and eosin staining). Squares represent high magnification (400×).
Histopathological analysis of the lung tissues from Acinetobacter baumannii- and Pseudomonas aeruginosa-infected mice. The lung tissues from C3H/HeN mice infected with ATCC 19606 (A, B, C, and D), TK1090 (E, F, G, and H), and PAO-1 (I, J, K, and L) strains and uninfected mouse (M) are shown. The lung tissues from the mice infected with ATCC 19606 at 1 day (A), 2 days (B), 5 days (C), and 14 days (D) post-infection. The lung tissues from the mice infected with TK1090 at 1 day (E), 2 days (F), 5 days (G), and 14 days (H) post-infection. The lung tissues from the mice infected with PAO-1 at 1 day (I), 2 days (J), 5 days (K), and 14 days (L) post-infection. Photomicrograph images (magnification, 100×; hematoxylin and eosin staining). Squares represent high magnification (400×).

Fig. 4.

Infiltration of neutrophils and macrophages in the lung tissues of Acinetobacter baumannii- and Pseudomonas aeruginosa-infected mice. The lung tissues from C3H/HeN mice infected with ATCC19606 (A, B, C, and D), TK1090 (E, F, G, and H), and PAO-1 (I, J, K, and L) strains and uninfected mice (M and N) are shown. The lung tissues from the mice infected with ATCC 19606 at 1 day (A and B) and 5 days (C and D) post-infection. The lung tissues from the mice infected with TK1090 at 1 day (E and F) and 5 days (G and H) post-infection. The lung tissues from the mice infected with PAO-1 at 1 day (I and J) and 5 days (K and L) post-infection. Neutrophils and macrophages were detected by immunostaining with anti-Ly-6G antibody (A, C, E, G, I, and K) and anti-CD68 antibody (B, D, F, H, J, and L) using diaminobenzidine (DAB) method and restained with hematoxylin, respectively. Photomicrograph images (magnification, 100×).
Infiltration of neutrophils and macrophages in the lung tissues of Acinetobacter baumannii- and Pseudomonas aeruginosa-infected mice. The lung tissues from C3H/HeN mice infected with ATCC19606 (A, B, C, and D), TK1090 (E, F, G, and H), and PAO-1 (I, J, K, and L) strains and uninfected mice (M and N) are shown. The lung tissues from the mice infected with ATCC 19606 at 1 day (A and B) and 5 days (C and D) post-infection. The lung tissues from the mice infected with TK1090 at 1 day (E and F) and 5 days (G and H) post-infection. The lung tissues from the mice infected with PAO-1 at 1 day (I and J) and 5 days (K and L) post-infection. Neutrophils and macrophages were detected by immunostaining with anti-Ly-6G antibody (A, C, E, G, I, and K) and anti-CD68 antibody (B, D, F, H, J, and L) using diaminobenzidine (DAB) method and restained with hematoxylin, respectively. Photomicrograph images (magnification, 100×).

Fig. 5.

Frequency of neutrophils and macrophages accumulated in the lung tissues of Acinetobacter baumannii- and Pseudomonas aeruginosa-infected mice. Infiltrated neutrophils and macrophages in the lung tissues of the infected mice were detected by monoclonal antibodies using diaminobenzidine (DAB) method and restained with hematoxylin, and were measured by the HALO image analysis system for counting of cell numbers. The frequencies of neutrophils (A) and macrophages (B) in the mice post-infection are shown. The frequencies of infected mice on day 2 and day 5 are shown as open and closed bars, respectively. Symbols indicate statistically significant differences (*p < 0.05, C3H/HeN mice infected with A. baumannii strains ATCC 19606 or TK1090 at 2 days post-infection vs. C3H/HeN mice infected with P. aeruginosa PAO-1 at 2 days post-infection, unpaired t-test; †p < 0.05, C3H/HeN mice infected with A. baumannii strains ATCC 19606 or TK1090 at 5 days post-infection vs. C3H/HeN mice infected with P. aeruginosa PAO-1 at 5 days post-infection, unpaired t-test).
Frequency of neutrophils and macrophages accumulated in the lung tissues of Acinetobacter baumannii- and Pseudomonas aeruginosa-infected mice. Infiltrated neutrophils and macrophages in the lung tissues of the infected mice were detected by monoclonal antibodies using diaminobenzidine (DAB) method and restained with hematoxylin, and were measured by the HALO image analysis system for counting of cell numbers. The frequencies of neutrophils (A) and macrophages (B) in the mice post-infection are shown. The frequencies of infected mice on day 2 and day 5 are shown as open and closed bars, respectively. Symbols indicate statistically significant differences (*p < 0.05, C3H/HeN mice infected with A. baumannii strains ATCC 19606 or TK1090 at 2 days post-infection vs. C3H/HeN mice infected with P. aeruginosa PAO-1 at 2 days post-infection, unpaired t-test; †p < 0.05, C3H/HeN mice infected with A. baumannii strains ATCC 19606 or TK1090 at 5 days post-infection vs. C3H/HeN mice infected with P. aeruginosa PAO-1 at 5 days post-infection, unpaired t-test).
Lingua:
Inglese
Frequenza di pubblicazione:
4 volte all'anno
Argomenti della rivista:
Scienze biologiche, Microbiologia e virologia
Feed RSS della rivista