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Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice

The antibiotic‐resistant Klebsiella pneumoniae (Kp) has become a significant crisis in treating pneumonia. Low‐frequency ultrasound (LFU) is promising to overcome the obstacles. Mice were infected with bioluminescent Kp Xen39 by intratracheal injection to study the therapeutic effect of LFU in combi...

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Autores principales: Yan, Kaicheng, Yang, Tianli, Xu, Juan, Dong, Liuhan, Wang, Jin, Cai, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618311/
https://www.ncbi.nlm.nih.gov/pubmed/36001465
http://dx.doi.org/10.1111/1751-7915.14134
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author Yan, Kaicheng
Yang, Tianli
Xu, Juan
Dong, Liuhan
Wang, Jin
Cai, Yun
author_facet Yan, Kaicheng
Yang, Tianli
Xu, Juan
Dong, Liuhan
Wang, Jin
Cai, Yun
author_sort Yan, Kaicheng
collection PubMed
description The antibiotic‐resistant Klebsiella pneumoniae (Kp) has become a significant crisis in treating pneumonia. Low‐frequency ultrasound (LFU) is promising to overcome the obstacles. Mice were infected with bioluminescent Kp Xen39 by intratracheal injection to study the therapeutic effect of LFU in combination with antibiotics. The counts per second (CPS) were assessed with an animal biophoton imaging system. Bacterial clearance, histopathology, and the concentrations of cytokines were determined to evaluate the therapeutic effect. LC–MS/MS was used to detect the distribution of antibiotics in the lung and plasma. LFU in combination with meropenem (MEM) or amikacin (AMK) significantly improved the behavioural state of mice. The CPS of the LFU combination group were more significantly decreased compared with those of the antibiotic alone groups. The average colony‐forming units of lung tissue in the LFU combination groups were also lower than those of the antibiotic groups. Although no significant changes of cytokines (IL‐6 and TNF‐α) in plasma and bronchoalveolar lavage fluid were observed, LFU in combination with antibiotics showed less inflammatory damage from histopathological results compared with the antibiotic‐alone groups. Moreover, 10 min of LFU treatment promoted the distribution of MEM and AMK in mouse lung tissue at 60 and 30 min, respectively, after dosage. LFU could enhance the effectiveness of MEM and AMK in the treatment of Kp‐induced pneumonia, which might be attributed to the fact that LFU could promote the distribution of antibiotics in lung tissue and reduce inflammatory injury.
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spelling pubmed-96183112022-11-01 Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice Yan, Kaicheng Yang, Tianli Xu, Juan Dong, Liuhan Wang, Jin Cai, Yun Microb Biotechnol Research Articles The antibiotic‐resistant Klebsiella pneumoniae (Kp) has become a significant crisis in treating pneumonia. Low‐frequency ultrasound (LFU) is promising to overcome the obstacles. Mice were infected with bioluminescent Kp Xen39 by intratracheal injection to study the therapeutic effect of LFU in combination with antibiotics. The counts per second (CPS) were assessed with an animal biophoton imaging system. Bacterial clearance, histopathology, and the concentrations of cytokines were determined to evaluate the therapeutic effect. LC–MS/MS was used to detect the distribution of antibiotics in the lung and plasma. LFU in combination with meropenem (MEM) or amikacin (AMK) significantly improved the behavioural state of mice. The CPS of the LFU combination group were more significantly decreased compared with those of the antibiotic alone groups. The average colony‐forming units of lung tissue in the LFU combination groups were also lower than those of the antibiotic groups. Although no significant changes of cytokines (IL‐6 and TNF‐α) in plasma and bronchoalveolar lavage fluid were observed, LFU in combination with antibiotics showed less inflammatory damage from histopathological results compared with the antibiotic‐alone groups. Moreover, 10 min of LFU treatment promoted the distribution of MEM and AMK in mouse lung tissue at 60 and 30 min, respectively, after dosage. LFU could enhance the effectiveness of MEM and AMK in the treatment of Kp‐induced pneumonia, which might be attributed to the fact that LFU could promote the distribution of antibiotics in lung tissue and reduce inflammatory injury. John Wiley and Sons Inc. 2022-08-24 /pmc/articles/PMC9618311/ /pubmed/36001465 http://dx.doi.org/10.1111/1751-7915.14134 Text en © 2022 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Yan, Kaicheng
Yang, Tianli
Xu, Juan
Dong, Liuhan
Wang, Jin
Cai, Yun
Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice
title Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice
title_full Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice
title_fullStr Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice
title_full_unstemmed Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice
title_short Synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of Klebsiella pneumoniae pneumonia in mice
title_sort synergistic effect of low‐frequency ultrasound and antibiotics on the treatment of klebsiella pneumoniae pneumonia in mice
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618311/
https://www.ncbi.nlm.nih.gov/pubmed/36001465
http://dx.doi.org/10.1111/1751-7915.14134
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