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Acanthamoeba and bacteria produce antimicrobials to target their counterpart

BACKGROUND: In the microbial ecosystem, microbes compete for space and nutrients. Consequently, some have developed the ability to kill or inhibit the growth of other competing microbes by producing antimicrobial substances. As the ‘producer’ species are generally immune to these substances, their c...

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Autores principales: Iqbal, Junaid, Siddiqui, Ruqaiyyah, Khan, Naveed Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929138/
https://www.ncbi.nlm.nih.gov/pubmed/24479709
http://dx.doi.org/10.1186/1756-3305-7-56
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author Iqbal, Junaid
Siddiqui, Ruqaiyyah
Khan, Naveed Ahmed
author_facet Iqbal, Junaid
Siddiqui, Ruqaiyyah
Khan, Naveed Ahmed
author_sort Iqbal, Junaid
collection PubMed
description BACKGROUND: In the microbial ecosystem, microbes compete for space and nutrients. Consequently, some have developed the ability to kill or inhibit the growth of other competing microbes by producing antimicrobial substances. As the ‘producer’ species are generally immune to these substances, their compounds act on the competing microbial species and give the producer more space and access to nutrients for growth. Many currently used antibiotics were developed by exploiting this potential of certain microbes. FINDINGS: Here, the free-living amoeba, Acanthamoeba castellanii, was investigated for its antibacterial activity against representative Gram positive and Gram negative bacteria, while bacterial isolates were tested for their anti-amoebic properties. Conditioned medium from A. castellanii showed remarkable bactericidal properties against methicillin-resistant Staphylococcus aureus (MRSA) exhibiting almost 100% kill rate, but had limited effect against Acinetobacter sp., Pseudomonas aeruginosa and vancomycin-resistant Enterococcus faecalis (VRE). Similarly, the conditioned medium of E. coli K1 and Enterobacter sp., exhibited potent anti-Acanthamoebic effects in a concentration-dependent manner. Conditioned media of Acanthamoeba, E. coli K1 and Enterobacter sp. showed no cytotoxicity in vitro when tested against human brain microvascular endothelial cells. Active molecule/s in aforementioned amoebic and two bacterial conditioned media were 5 – 10 kDa, and <5 kDa respectively. CONCLUSIONS: A. castellanii conditioned medium showed potent bactericidal properties against MRSA. The active molecule(s) are heat- and pronase-resistant, and in the 5 to 10 kDa molecular mass range. Contrary to this, E. coli K1 and Enterobacter sp., conditioned medium showed anti-amoebic effects that are <5 kDa in molecular mass, suggestive of active metabolites.
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spelling pubmed-39291382014-02-20 Acanthamoeba and bacteria produce antimicrobials to target their counterpart Iqbal, Junaid Siddiqui, Ruqaiyyah Khan, Naveed Ahmed Parasit Vectors Short Report BACKGROUND: In the microbial ecosystem, microbes compete for space and nutrients. Consequently, some have developed the ability to kill or inhibit the growth of other competing microbes by producing antimicrobial substances. As the ‘producer’ species are generally immune to these substances, their compounds act on the competing microbial species and give the producer more space and access to nutrients for growth. Many currently used antibiotics were developed by exploiting this potential of certain microbes. FINDINGS: Here, the free-living amoeba, Acanthamoeba castellanii, was investigated for its antibacterial activity against representative Gram positive and Gram negative bacteria, while bacterial isolates were tested for their anti-amoebic properties. Conditioned medium from A. castellanii showed remarkable bactericidal properties against methicillin-resistant Staphylococcus aureus (MRSA) exhibiting almost 100% kill rate, but had limited effect against Acinetobacter sp., Pseudomonas aeruginosa and vancomycin-resistant Enterococcus faecalis (VRE). Similarly, the conditioned medium of E. coli K1 and Enterobacter sp., exhibited potent anti-Acanthamoebic effects in a concentration-dependent manner. Conditioned media of Acanthamoeba, E. coli K1 and Enterobacter sp. showed no cytotoxicity in vitro when tested against human brain microvascular endothelial cells. Active molecule/s in aforementioned amoebic and two bacterial conditioned media were 5 – 10 kDa, and <5 kDa respectively. CONCLUSIONS: A. castellanii conditioned medium showed potent bactericidal properties against MRSA. The active molecule(s) are heat- and pronase-resistant, and in the 5 to 10 kDa molecular mass range. Contrary to this, E. coli K1 and Enterobacter sp., conditioned medium showed anti-amoebic effects that are <5 kDa in molecular mass, suggestive of active metabolites. BioMed Central 2014-01-30 /pmc/articles/PMC3929138/ /pubmed/24479709 http://dx.doi.org/10.1186/1756-3305-7-56 Text en Copyright © 2014 Iqbal et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Iqbal, Junaid
Siddiqui, Ruqaiyyah
Khan, Naveed Ahmed
Acanthamoeba and bacteria produce antimicrobials to target their counterpart
title Acanthamoeba and bacteria produce antimicrobials to target their counterpart
title_full Acanthamoeba and bacteria produce antimicrobials to target their counterpart
title_fullStr Acanthamoeba and bacteria produce antimicrobials to target their counterpart
title_full_unstemmed Acanthamoeba and bacteria produce antimicrobials to target their counterpart
title_short Acanthamoeba and bacteria produce antimicrobials to target their counterpart
title_sort acanthamoeba and bacteria produce antimicrobials to target their counterpart
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929138/
https://www.ncbi.nlm.nih.gov/pubmed/24479709
http://dx.doi.org/10.1186/1756-3305-7-56
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