Variables Affecting the Recovery of <i>Acanthamoeba</i> Trophozoites
While the results of <i>Acanthamoeba </i>testing have been extensively published, laboratories conducting such testing are left to develop their own methods in the absence of a standardized methodology. The wide disparity of methods has resulted in equally inconsistent reported results f...
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doaj-12eadc3296d843fbbef87d88061cfd6a2021-02-19T00:04:06ZengMDPI AGPathogens2076-08172021-02-011022122110.3390/pathogens10020221Variables Affecting the Recovery of <i>Acanthamoeba</i> TrophozoitesMonica J. Crary0Rhonda Walters1Paul Shannon2Manal M. Gabriel3R&D Microbiology, Alcon Research, LLC, Fort Worth, TX 76134, USAR&D Microbiology, Alcon Research, LLC, Fort Worth, TX 76134, USAR&D Microbiology, Alcon Research, LLC, Fort Worth, TX 76134, USAR&D Microbiology, Alcon Research, LLC, Fort Worth, TX 76134, USAWhile the results of <i>Acanthamoeba </i>testing have been extensively published, laboratories conducting such testing are left to develop their own methods in the absence of a standardized methodology. The wide disparity of methods has resulted in equally inconsistent reported results for contact lens care (CLC) products. This study’s objective was to determine the source of these discrepancies by evaluating basic <i>Acanthamoeba</i> biology and their impact on antimicrobial efficacy testing, including the ability of a recovery method to stimulate a single trophozoite to proliferate. Antimicrobial efficacy testing was conducted using well-published <i>Acanthamoeba</i> strains, storage conditions, and growth-based recovery methods. To identify variables that influence results, test solutions with low <i>Acanthamoeba</i> disinfection rates were utilized to prevent differences from being masked by high log reductions. In addition, single-cell proliferation assays were executed to understand the growth requirements to stimulate trophozoite propagation in two recovery methods. These studies indicated that both nutrient density (>10<sup>6 </sup>CFU) and the length of plate incubation (at least 14 days) could significantly influence the accurate recovery of trophozoites. Together, this study emphasizes the need to understand how <i>Acanthamoeba</i> trophozoites biology can impact test methods to create divergent results.https://www.mdpi.com/2076-0817/10/2/221<i>Acanthamoeba</i>contact lens careefficacy testingtrophozoites |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Monica J. Crary Rhonda Walters Paul Shannon Manal M. Gabriel |
spellingShingle |
Monica J. Crary Rhonda Walters Paul Shannon Manal M. Gabriel Variables Affecting the Recovery of <i>Acanthamoeba</i> Trophozoites Pathogens <i>Acanthamoeba</i> contact lens care efficacy testing trophozoites |
author_facet |
Monica J. Crary Rhonda Walters Paul Shannon Manal M. Gabriel |
author_sort |
Monica J. Crary |
title |
Variables Affecting the Recovery of <i>Acanthamoeba</i> Trophozoites |
title_short |
Variables Affecting the Recovery of <i>Acanthamoeba</i> Trophozoites |
title_full |
Variables Affecting the Recovery of <i>Acanthamoeba</i> Trophozoites |
title_fullStr |
Variables Affecting the Recovery of <i>Acanthamoeba</i> Trophozoites |
title_full_unstemmed |
Variables Affecting the Recovery of <i>Acanthamoeba</i> Trophozoites |
title_sort |
variables affecting the recovery of <i>acanthamoeba</i> trophozoites |
publisher |
MDPI AG |
series |
Pathogens |
issn |
2076-0817 |
publishDate |
2021-02-01 |
description |
While the results of <i>Acanthamoeba </i>testing have been extensively published, laboratories conducting such testing are left to develop their own methods in the absence of a standardized methodology. The wide disparity of methods has resulted in equally inconsistent reported results for contact lens care (CLC) products. This study’s objective was to determine the source of these discrepancies by evaluating basic <i>Acanthamoeba</i> biology and their impact on antimicrobial efficacy testing, including the ability of a recovery method to stimulate a single trophozoite to proliferate. Antimicrobial efficacy testing was conducted using well-published <i>Acanthamoeba</i> strains, storage conditions, and growth-based recovery methods. To identify variables that influence results, test solutions with low <i>Acanthamoeba</i> disinfection rates were utilized to prevent differences from being masked by high log reductions. In addition, single-cell proliferation assays were executed to understand the growth requirements to stimulate trophozoite propagation in two recovery methods. These studies indicated that both nutrient density (>10<sup>6 </sup>CFU) and the length of plate incubation (at least 14 days) could significantly influence the accurate recovery of trophozoites. Together, this study emphasizes the need to understand how <i>Acanthamoeba</i> trophozoites biology can impact test methods to create divergent results. |
topic |
<i>Acanthamoeba</i> contact lens care efficacy testing trophozoites |
url |
https://www.mdpi.com/2076-0817/10/2/221 |
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