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Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii

With the growing emergence of pan-drug-resistant Acinetobacter baumannii (PDR-Ab) strains in clinical, new strategies for the treatment of PDR-Ab infections are urgently needed. Egg yolk immunoglobulin (IgY) as a convenient and inexpensive antibody has been widely applied to the therapy of infectiou...

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Autores principales: Shi, Huaying, Zhu, Jie, Zou, Boyang, Shi, Lei, Du, Linying, Long, Yayi, Wang, Huaxin, Xu, Hong, Zhen, Yuhong, Sun, Lidan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Masson SAS. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126593/
https://www.ncbi.nlm.nih.gov/pubmed/28962078
http://dx.doi.org/10.1016/j.biopha.2017.09.112
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author Shi, Huaying
Zhu, Jie
Zou, Boyang
Shi, Lei
Du, Linying
Long, Yayi
Wang, Huaxin
Xu, Hong
Zhen, Yuhong
Sun, Lidan
author_facet Shi, Huaying
Zhu, Jie
Zou, Boyang
Shi, Lei
Du, Linying
Long, Yayi
Wang, Huaxin
Xu, Hong
Zhen, Yuhong
Sun, Lidan
author_sort Shi, Huaying
collection PubMed
description With the growing emergence of pan-drug-resistant Acinetobacter baumannii (PDR-Ab) strains in clinical, new strategies for the treatment of PDR-Ab infections are urgently needed. Egg yolk immunoglobulin (IgY) as a convenient and inexpensive antibody has been widely applied to the therapy of infectious diseases. The aim of this study was to produce IgY specific to PDR-Ab and investigate its antibacterial effects in vitro and in vivo. IgYs specific to two PDR-Ab strains were produced by immunizing hens with formaldehyde inactivated PDR-Ab cells and isolated from yolks with a purity of 90% by water dilution, salt precipitations and ultrafiltration. IgYs showed high titers when subjected to an ELISA and inhibited the growth of PDR-Ab in a dose-dependent manner in liquid medium. Scanning electron microscopy assay showed structural modification and aggregation of PDR-Ab treated with specific IgYs. Freshly cultured PDR-Ab cells were nasally inhaled in BALB/c mice to induce acute pneumonia. The infected mice were intraperitoneally injected with specific IgYs using cefoperazone/sulbactam and dexamethasone as positive controls. The IgYs specific to PDR-Ab lowered the mortality of mice with PDR-Ab-induced acute pneumonia, decreased the level of TNF-α and IL-1β in serum and reduced inflammation in lung tissue. Specific IgY has the potential to be used as a new therapeutic approach for the treatment of A. baumannii-induced infections.
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spelling pubmed-71265932020-04-08 Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii Shi, Huaying Zhu, Jie Zou, Boyang Shi, Lei Du, Linying Long, Yayi Wang, Huaxin Xu, Hong Zhen, Yuhong Sun, Lidan Biomed Pharmacother Original Article With the growing emergence of pan-drug-resistant Acinetobacter baumannii (PDR-Ab) strains in clinical, new strategies for the treatment of PDR-Ab infections are urgently needed. Egg yolk immunoglobulin (IgY) as a convenient and inexpensive antibody has been widely applied to the therapy of infectious diseases. The aim of this study was to produce IgY specific to PDR-Ab and investigate its antibacterial effects in vitro and in vivo. IgYs specific to two PDR-Ab strains were produced by immunizing hens with formaldehyde inactivated PDR-Ab cells and isolated from yolks with a purity of 90% by water dilution, salt precipitations and ultrafiltration. IgYs showed high titers when subjected to an ELISA and inhibited the growth of PDR-Ab in a dose-dependent manner in liquid medium. Scanning electron microscopy assay showed structural modification and aggregation of PDR-Ab treated with specific IgYs. Freshly cultured PDR-Ab cells were nasally inhaled in BALB/c mice to induce acute pneumonia. The infected mice were intraperitoneally injected with specific IgYs using cefoperazone/sulbactam and dexamethasone as positive controls. The IgYs specific to PDR-Ab lowered the mortality of mice with PDR-Ab-induced acute pneumonia, decreased the level of TNF-α and IL-1β in serum and reduced inflammation in lung tissue. Specific IgY has the potential to be used as a new therapeutic approach for the treatment of A. baumannii-induced infections. Elsevier Masson SAS. 2017-11 2017-10-06 /pmc/articles/PMC7126593/ /pubmed/28962078 http://dx.doi.org/10.1016/j.biopha.2017.09.112 Text en © 2017 Elsevier Masson SAS. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Original Article
Shi, Huaying
Zhu, Jie
Zou, Boyang
Shi, Lei
Du, Linying
Long, Yayi
Wang, Huaxin
Xu, Hong
Zhen, Yuhong
Sun, Lidan
Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii
title Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii
title_full Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii
title_fullStr Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii
title_full_unstemmed Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii
title_short Effects of specific egg yolk immunoglobulin on pan-drug-resistant Acinetobacter baumannii
title_sort effects of specific egg yolk immunoglobulin on pan-drug-resistant acinetobacter baumannii
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126593/
https://www.ncbi.nlm.nih.gov/pubmed/28962078
http://dx.doi.org/10.1016/j.biopha.2017.09.112
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