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The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage

BACKGROUND: Widespread misuse of antibiotics caused bacterial resistance increasingly become a serious threat. Bacteriophage therapy promises alternative treatment strategies for combatting drug-resistant bacterial infections. In this study, we isolated and characterized a novel, potent lytic bacter...

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Autores principales: Sisakhtpour, Behnam, Mirzaei, Arezoo, Karbasizadeh, Vajihe, Hosseini, Nafiseh, Shabani, Mehdi, Moghim, Sharareh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742398/
https://www.ncbi.nlm.nih.gov/pubmed/34996464
http://dx.doi.org/10.1186/s12941-022-00492-9
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author Sisakhtpour, Behnam
Mirzaei, Arezoo
Karbasizadeh, Vajihe
Hosseini, Nafiseh
Shabani, Mehdi
Moghim, Sharareh
author_facet Sisakhtpour, Behnam
Mirzaei, Arezoo
Karbasizadeh, Vajihe
Hosseini, Nafiseh
Shabani, Mehdi
Moghim, Sharareh
author_sort Sisakhtpour, Behnam
collection PubMed
description BACKGROUND: Widespread misuse of antibiotics caused bacterial resistance increasingly become a serious threat. Bacteriophage therapy promises alternative treatment strategies for combatting drug-resistant bacterial infections. In this study, we isolated and characterized a novel, potent lytic bacteriophage against multi-drug resistant (MDR) Acinetobacter baumannii and described the lytic capability and endolysin activity of the phage to evaluate the potential in phage therapy. METHODS: A novel phage, pIsf-AB02, was isolated from hospital sewage. The morphological analysis, its host range, growth characteristics, stability under various conditions, genomic restriction pattern were systematically investigated. The protein pattern of the phage was analyzed, and the endolysin activity of the phage was determined under the non-denaturing condition on SDS-PAGE. The optimal lytic titer of phage was assessed by co-culture of the phage with clinical MDR A. baumannii isolates. Finally, HeLa cells were used to examine the safety of the phage. RESULTS: The morphological analysis revealed that the pIsf-AB02 phage displays morphology resembling the Myoviridae family. It can quickly destroy 56.3% (27/48) of clinical MDR A. baumannii isolates. This virulent phage could decrease the bacterial host cells (from 10(8) CFU/ml to 10(3) CFU/ml) in 30 min. The optimum stability of the phage was observed at 37 °C. pH 7 is the most suitable condition to maintain phage stability. The 15 kDa protein encoded by pIsf-AB02 was detected to have endolysin activity. pIsf-AB02 did not show cytotoxicity to HeLa cells, and it can save HeLa cells from A. baumannii infection. CONCLUSION: In this study, we isolated a novel lytic MDR A. baumannii bacteriophage, pIsf-AB02. This phage showed suitable stability at different temperatures and pHs, and demonstrated potent in vitro endolysin activity. pIsf-AB02 may be a good candidate as a therapeutic agent to control nosocomial infections caused by MDR A. baumannii. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-022-00492-9.
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spelling pubmed-87423982022-01-10 The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage Sisakhtpour, Behnam Mirzaei, Arezoo Karbasizadeh, Vajihe Hosseini, Nafiseh Shabani, Mehdi Moghim, Sharareh Ann Clin Microbiol Antimicrob Research BACKGROUND: Widespread misuse of antibiotics caused bacterial resistance increasingly become a serious threat. Bacteriophage therapy promises alternative treatment strategies for combatting drug-resistant bacterial infections. In this study, we isolated and characterized a novel, potent lytic bacteriophage against multi-drug resistant (MDR) Acinetobacter baumannii and described the lytic capability and endolysin activity of the phage to evaluate the potential in phage therapy. METHODS: A novel phage, pIsf-AB02, was isolated from hospital sewage. The morphological analysis, its host range, growth characteristics, stability under various conditions, genomic restriction pattern were systematically investigated. The protein pattern of the phage was analyzed, and the endolysin activity of the phage was determined under the non-denaturing condition on SDS-PAGE. The optimal lytic titer of phage was assessed by co-culture of the phage with clinical MDR A. baumannii isolates. Finally, HeLa cells were used to examine the safety of the phage. RESULTS: The morphological analysis revealed that the pIsf-AB02 phage displays morphology resembling the Myoviridae family. It can quickly destroy 56.3% (27/48) of clinical MDR A. baumannii isolates. This virulent phage could decrease the bacterial host cells (from 10(8) CFU/ml to 10(3) CFU/ml) in 30 min. The optimum stability of the phage was observed at 37 °C. pH 7 is the most suitable condition to maintain phage stability. The 15 kDa protein encoded by pIsf-AB02 was detected to have endolysin activity. pIsf-AB02 did not show cytotoxicity to HeLa cells, and it can save HeLa cells from A. baumannii infection. CONCLUSION: In this study, we isolated a novel lytic MDR A. baumannii bacteriophage, pIsf-AB02. This phage showed suitable stability at different temperatures and pHs, and demonstrated potent in vitro endolysin activity. pIsf-AB02 may be a good candidate as a therapeutic agent to control nosocomial infections caused by MDR A. baumannii. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12941-022-00492-9. BioMed Central 2022-01-07 /pmc/articles/PMC8742398/ /pubmed/34996464 http://dx.doi.org/10.1186/s12941-022-00492-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sisakhtpour, Behnam
Mirzaei, Arezoo
Karbasizadeh, Vajihe
Hosseini, Nafiseh
Shabani, Mehdi
Moghim, Sharareh
The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage
title The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage
title_full The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage
title_fullStr The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage
title_full_unstemmed The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage
title_short The characteristic and potential therapeutic effect of isolated multidrug-resistant Acinetobacter baumannii lytic phage
title_sort characteristic and potential therapeutic effect of isolated multidrug-resistant acinetobacter baumannii lytic phage
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742398/
https://www.ncbi.nlm.nih.gov/pubmed/34996464
http://dx.doi.org/10.1186/s12941-022-00492-9
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