Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal Phase

The biofilm-forming potential of <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i>, isolated from patients with Endophthalmitis, was monitored using glass cover slips and cadaveric corneas as substrata. Both the ocular fluid isolates exhibited biofilm-forming...

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Main Authors: Ranjith Konduri, Chinthala Reddy Saiabhilash, Sisinthy Shivaji
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Microorganisms
Subjects:
eye
Online Access:https://www.mdpi.com/2076-2607/9/6/1124
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spelling doaj-24fa760255ee462e926a772c241be30c2021-06-01T00:49:11ZengMDPI AGMicroorganisms2076-26072021-05-0191124112410.3390/microorganisms9061124Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal PhaseRanjith Konduri0Chinthala Reddy Saiabhilash1Sisinthy Shivaji2Jhaveri Microbiology Centre, Prof. Brien Holden Eye Research Centre, Kallam Anji Reddy Campus, L. V. Prasad Eye Institute, Hyderabad 500034, Telangana, IndiaJhaveri Microbiology Centre, Prof. Brien Holden Eye Research Centre, Kallam Anji Reddy Campus, L. V. Prasad Eye Institute, Hyderabad 500034, Telangana, IndiaJhaveri Microbiology Centre, Prof. Brien Holden Eye Research Centre, Kallam Anji Reddy Campus, L. V. Prasad Eye Institute, Hyderabad 500034, Telangana, IndiaThe biofilm-forming potential of <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i>, isolated from patients with Endophthalmitis, was monitored using glass cover slips and cadaveric corneas as substrata. Both the ocular fluid isolates exhibited biofilm-forming potential by the Congo red agar, Crystal violet and 2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-(phenylamino) carbonyl-2H-tetra-zolium hydroxide (XTT) methods. Confocal microscopy demonstrated that the thickness of the biofilm increased from 4–120 h of biofilm formation. Scanning electron microscopic studies indicated that the biofilms grown on cover slips and ex vivo corneas of both the isolates go through an adhesion phase at 4 h followed by multilayer clumping of cells with intercellular connections and copious amounts of extracellular polymeric substance. Clumps subsequently formed columns and eventually single cells were visible indicative of dispersal phase. Biofilm formation was more rapid when the cornea was used as a substratum. In the biofilms grown on corneas, clumping of cells, formation of 3D structures and final appearance of single cells indicative of dispersal phase occurred by 48 h compared to 96–120 h when biofilms were grown on cover slips. In the biofilm phase, both were several-fold more resistant to antibiotics compared to planktonic cells. This is the first study on biofilm forming potential of ocular fluid <i>S. aureus</i> and <i>S. epidermidis</i> on cadaveric cornea, from attachment to dispersal phase of biofilm formation.https://www.mdpi.com/2076-2607/9/6/1124biofilmocular fluidantimicrobial resistanceeye<i>S. aureus</i><i>S. epidermidis</i>
collection DOAJ
language English
format Article
sources DOAJ
author Ranjith Konduri
Chinthala Reddy Saiabhilash
Sisinthy Shivaji
spellingShingle Ranjith Konduri
Chinthala Reddy Saiabhilash
Sisinthy Shivaji
Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal Phase
Microorganisms
biofilm
ocular fluid
antimicrobial resistance
eye
<i>S. aureus</i>
<i>S. epidermidis</i>
author_facet Ranjith Konduri
Chinthala Reddy Saiabhilash
Sisinthy Shivaji
author_sort Ranjith Konduri
title Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal Phase
title_short Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal Phase
title_full Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal Phase
title_fullStr Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal Phase
title_full_unstemmed Biofilm-Forming Potential of Ocular Fluid <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i> on Ex Vivo Human Corneas from Attachment to Dispersal Phase
title_sort biofilm-forming potential of ocular fluid <i>staphylococcus aureus</i> and <i>staphylococcus epidermidis</i> on ex vivo human corneas from attachment to dispersal phase
publisher MDPI AG
series Microorganisms
issn 2076-2607
publishDate 2021-05-01
description The biofilm-forming potential of <i>Staphylococcus aureus</i> and <i>Staphylococcus epidermidis</i>, isolated from patients with Endophthalmitis, was monitored using glass cover slips and cadaveric corneas as substrata. Both the ocular fluid isolates exhibited biofilm-forming potential by the Congo red agar, Crystal violet and 2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-(phenylamino) carbonyl-2H-tetra-zolium hydroxide (XTT) methods. Confocal microscopy demonstrated that the thickness of the biofilm increased from 4–120 h of biofilm formation. Scanning electron microscopic studies indicated that the biofilms grown on cover slips and ex vivo corneas of both the isolates go through an adhesion phase at 4 h followed by multilayer clumping of cells with intercellular connections and copious amounts of extracellular polymeric substance. Clumps subsequently formed columns and eventually single cells were visible indicative of dispersal phase. Biofilm formation was more rapid when the cornea was used as a substratum. In the biofilms grown on corneas, clumping of cells, formation of 3D structures and final appearance of single cells indicative of dispersal phase occurred by 48 h compared to 96–120 h when biofilms were grown on cover slips. In the biofilm phase, both were several-fold more resistant to antibiotics compared to planktonic cells. This is the first study on biofilm forming potential of ocular fluid <i>S. aureus</i> and <i>S. epidermidis</i> on cadaveric cornea, from attachment to dispersal phase of biofilm formation.
topic biofilm
ocular fluid
antimicrobial resistance
eye
<i>S. aureus</i>
<i>S. epidermidis</i>
url https://www.mdpi.com/2076-2607/9/6/1124
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