Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicans

Candida sp. impelled opportunistic infection in immune-compromised patients ensuing from asymptomatic colonization to pathogenic forms. Moreover, slow spread of Candida species inducing refractory mucosal and invasive infections brings acute resistance to antifungal drugs. Hence, here we probed the...

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Main Authors: Shahper N. Khan, Shakir Khan, Jawed Iqbal, Rosina Khan, Asad U. Khan
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-08-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmicb.2017.01641/full
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spelling doaj-9f77cea7ec104462a798030ee1a524732020-11-24T23:11:57ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2017-08-01810.3389/fmicb.2017.01641283106Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicansShahper N. KhanShakir KhanJawed IqbalRosina KhanAsad U. KhanCandida sp. impelled opportunistic infection in immune-compromised patients ensuing from asymptomatic colonization to pathogenic forms. Moreover, slow spread of Candida species inducing refractory mucosal and invasive infections brings acute resistance to antifungal drugs. Hence, here we probed the effect of encapsulated preparation of cinnamaldehyde (CNMA) in multilamellar liposomes (ML) against Candida albicans. The efficacy of ML-CNMA against Candida biofilm was assessed by scanning electron microscopy, transmission electron microscopy, as well as light microscopy and its percent inhibition, was determined by XTT [2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide] and crystal violet assay. ML-CNMA showed more fungicidal activity than free CNMA as well as multilamellar liposomal amphotericin B (ML-Amp B), which was further confirmed by spot test assay and Log-logistic dose–response analysis. Antifungal activity was driven by reactive oxygen species and cellular damage by sustained release of CNMA. Effect on hyphal formation during 48 h in presence/absence of ML-CNMA was observed under a microscope and further substantiated by RT-PCR by amplifying HWP1, the gene responsible for hyphal wall protein formation. Apoptotic programmed cell death was analyzed by FACS analysis which was further confirmed by cytochrome C release assay. This study elucidates the mechanistic insight of the enhanced antifungal activity of ML preparation of CNMA against Candida infections.http://journal.frontiersin.org/article/10.3389/fmicb.2017.01641/fullCNMAmultilamellar liposomeapoptosisbiofilmCandida albicans
collection DOAJ
language English
format Article
sources DOAJ
author Shahper N. Khan
Shakir Khan
Jawed Iqbal
Rosina Khan
Asad U. Khan
spellingShingle Shahper N. Khan
Shakir Khan
Jawed Iqbal
Rosina Khan
Asad U. Khan
Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicans
Frontiers in Microbiology
CNMA
multilamellar liposome
apoptosis
biofilm
Candida albicans
author_facet Shahper N. Khan
Shakir Khan
Jawed Iqbal
Rosina Khan
Asad U. Khan
author_sort Shahper N. Khan
title Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicans
title_short Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicans
title_full Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicans
title_fullStr Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicans
title_full_unstemmed Enhanced Killing and Antibiofilm Activity of Encapsulated Cinnamaldehyde against Candida albicans
title_sort enhanced killing and antibiofilm activity of encapsulated cinnamaldehyde against candida albicans
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2017-08-01
description Candida sp. impelled opportunistic infection in immune-compromised patients ensuing from asymptomatic colonization to pathogenic forms. Moreover, slow spread of Candida species inducing refractory mucosal and invasive infections brings acute resistance to antifungal drugs. Hence, here we probed the effect of encapsulated preparation of cinnamaldehyde (CNMA) in multilamellar liposomes (ML) against Candida albicans. The efficacy of ML-CNMA against Candida biofilm was assessed by scanning electron microscopy, transmission electron microscopy, as well as light microscopy and its percent inhibition, was determined by XTT [2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide] and crystal violet assay. ML-CNMA showed more fungicidal activity than free CNMA as well as multilamellar liposomal amphotericin B (ML-Amp B), which was further confirmed by spot test assay and Log-logistic dose–response analysis. Antifungal activity was driven by reactive oxygen species and cellular damage by sustained release of CNMA. Effect on hyphal formation during 48 h in presence/absence of ML-CNMA was observed under a microscope and further substantiated by RT-PCR by amplifying HWP1, the gene responsible for hyphal wall protein formation. Apoptotic programmed cell death was analyzed by FACS analysis which was further confirmed by cytochrome C release assay. This study elucidates the mechanistic insight of the enhanced antifungal activity of ML preparation of CNMA against Candida infections.
topic CNMA
multilamellar liposome
apoptosis
biofilm
Candida albicans
url http://journal.frontiersin.org/article/10.3389/fmicb.2017.01641/full
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