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Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures
Patient-derived organoids are a useful platform for identification and testing of novel precision oncology approaches. Patient-derived organoids are generated by direct culture of patient samples. However, prior to development into patient-derived organoids, these samples are often processed for cli...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for Cancer Research
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530407/ https://www.ncbi.nlm.nih.gov/pubmed/37772998 http://dx.doi.org/10.1158/2767-9764.CRC-23-0109 |
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author | Dayanidhi, Divya L. Watlington, Wylie K. Mantyh, John B. Rupprecht, Gabrielle Hsu, David S. |
author_facet | Dayanidhi, Divya L. Watlington, Wylie K. Mantyh, John B. Rupprecht, Gabrielle Hsu, David S. |
author_sort | Dayanidhi, Divya L. |
collection | PubMed |
description | Patient-derived organoids are a useful platform for identification and testing of novel precision oncology approaches. Patient-derived organoids are generated by direct culture of patient samples. However, prior to development into patient-derived organoids, these samples are often processed for clinical use, opening the potential for contamination by Mycoplasma and other microbes. While most microbes can be detected by visual inspection, Mycoplasma can go undetected and have substantial impacts on assay results. Given the increased use of patient-derived organoids, there is a growing need for a standardized protocol to detect and remove Mycoplasma from organoid models. In the current study, we report a procedure for Mycoplasma removal by passaging organoids through mice as patient-derived organoid xenografts. In vivo passage of patient-derived organoids followed by re-establishment was 100% effective at decontaminating colorectal patient-derived organoids (n = 9), based on testing with the Sigma LookOut Mycoplasma PCR Detection Kit. This process can serve as a method to re-establish contaminated patient-derived organoids, which represent precious models to study patient-specific genomic features and treatment responses. SIGNIFICANCE: Organoids are valuable models of cancer. Mycoplasma contamination can alter organoid drug sensitivity, so there is a need for a standardized protocol to detect and remove Mycoplasma from organoids. We report a simple procedure for removing Mycoplasma from organoids via in vivo passaging through mice followed by re-establishment of organoids. |
format | Online Article Text |
id | pubmed-10530407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for Cancer Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-105304072023-09-28 Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures Dayanidhi, Divya L. Watlington, Wylie K. Mantyh, John B. Rupprecht, Gabrielle Hsu, David S. Cancer Res Commun Research Article Patient-derived organoids are a useful platform for identification and testing of novel precision oncology approaches. Patient-derived organoids are generated by direct culture of patient samples. However, prior to development into patient-derived organoids, these samples are often processed for clinical use, opening the potential for contamination by Mycoplasma and other microbes. While most microbes can be detected by visual inspection, Mycoplasma can go undetected and have substantial impacts on assay results. Given the increased use of patient-derived organoids, there is a growing need for a standardized protocol to detect and remove Mycoplasma from organoid models. In the current study, we report a procedure for Mycoplasma removal by passaging organoids through mice as patient-derived organoid xenografts. In vivo passage of patient-derived organoids followed by re-establishment was 100% effective at decontaminating colorectal patient-derived organoids (n = 9), based on testing with the Sigma LookOut Mycoplasma PCR Detection Kit. This process can serve as a method to re-establish contaminated patient-derived organoids, which represent precious models to study patient-specific genomic features and treatment responses. SIGNIFICANCE: Organoids are valuable models of cancer. Mycoplasma contamination can alter organoid drug sensitivity, so there is a need for a standardized protocol to detect and remove Mycoplasma from organoids. We report a simple procedure for removing Mycoplasma from organoids via in vivo passaging through mice followed by re-establishment of organoids. American Association for Cancer Research 2023-09-27 /pmc/articles/PMC10530407/ /pubmed/37772998 http://dx.doi.org/10.1158/2767-9764.CRC-23-0109 Text en © 2023 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by/4.0/This open access article is distributed under the Creative Commons Attribution 4.0 International (CC BY 4.0) license. |
spellingShingle | Research Article Dayanidhi, Divya L. Watlington, Wylie K. Mantyh, John B. Rupprecht, Gabrielle Hsu, David S. Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures |
title | Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures |
title_full | Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures |
title_fullStr | Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures |
title_full_unstemmed | Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures |
title_short | Effects and Eradication of Mycoplasma Contamination on Patient-derived Colorectal Cancer Organoid Cultures |
title_sort | effects and eradication of mycoplasma contamination on patient-derived colorectal cancer organoid cultures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530407/ https://www.ncbi.nlm.nih.gov/pubmed/37772998 http://dx.doi.org/10.1158/2767-9764.CRC-23-0109 |
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