Cargando…
The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11
BACKGROUND: Candida albicans, the main human fungal pathogen, can cause fungal infection and seriously affect people's health and life. This study aimed to investigate the effects of ritonavir (RIT) on C. albicans and the correlation between SAP2 as well as ERG11 and drug resistance. RESULTS: S...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342201/ https://www.ncbi.nlm.nih.gov/pubmed/33951330 http://dx.doi.org/10.1002/iid3.415 |
_version_ | 1783734018828664832 |
---|---|
author | Feng, Wenli Yang, Jing Ma, Yan Xi, Zhiqin Zhao, Xiaoqin Zhao, Xiaoxia Zhao, Min |
author_facet | Feng, Wenli Yang, Jing Ma, Yan Xi, Zhiqin Zhao, Xiaoqin Zhao, Xiaoxia Zhao, Min |
author_sort | Feng, Wenli |
collection | PubMed |
description | BACKGROUND: Candida albicans, the main human fungal pathogen, can cause fungal infection and seriously affect people's health and life. This study aimed to investigate the effects of ritonavir (RIT) on C. albicans and the correlation between SAP2 as well as ERG11 and drug resistance. RESULTS: Secreted aspartyl proteinases (Saps) activities and pathogenicity of C. albicans with different drug resistance were measured. M27‐A4 broth microdilution method was used to analyze the drug sensitivity of RIT combined with fluconazole (FCA) on C. albicans. After that, SAP2 and ERG11 mutations were examined by polymerase chain reaction (PCR) and sequencing, and quantitative real‐time PCR was utilized to determine the expression of the two genes. By analyzing pz values, the Saps activity of cross‐resistant strains was the highest, followed by voriconazole (VRC)‐resistant strains, FCA‐resistant strains, itraconazole (ITR)‐resistant strains, and sensitive strains. The pathogenicity of C. albicans in descending order was as follows: cross‐resistant strains, VRC‐resistant strains, ITR‐resistant strains, FCA‐resistant strains, and sensitive strains. With the increase of RIT concentrations, the Saps activity was gradually inhibited. Drug sensitivity results showed that there was no synergistic effect between RIT and FCA. Additionally, no gene mutation sites were found in SAP2 sequencing, and 17 synonymous mutations and 6 missense mutations occurred in ERG11 sequencing. Finally, the expression of SAP2 and ERG11 was significantly higher in the resistant strains compared with the sensitive strains, and there was a positive liner correlation between SAP2 and ERG11 messenger RNA expression (r = .6655, p < .001). CONCLUSION: These findings may help to improve our understanding of azole‐resistant mechanisms of C. albicans and provide a novel direction for clinical therapeutics of C. albicans infection. |
format | Online Article Text |
id | pubmed-8342201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83422012021-08-11 The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11 Feng, Wenli Yang, Jing Ma, Yan Xi, Zhiqin Zhao, Xiaoqin Zhao, Xiaoxia Zhao, Min Immun Inflamm Dis Original Research BACKGROUND: Candida albicans, the main human fungal pathogen, can cause fungal infection and seriously affect people's health and life. This study aimed to investigate the effects of ritonavir (RIT) on C. albicans and the correlation between SAP2 as well as ERG11 and drug resistance. RESULTS: Secreted aspartyl proteinases (Saps) activities and pathogenicity of C. albicans with different drug resistance were measured. M27‐A4 broth microdilution method was used to analyze the drug sensitivity of RIT combined with fluconazole (FCA) on C. albicans. After that, SAP2 and ERG11 mutations were examined by polymerase chain reaction (PCR) and sequencing, and quantitative real‐time PCR was utilized to determine the expression of the two genes. By analyzing pz values, the Saps activity of cross‐resistant strains was the highest, followed by voriconazole (VRC)‐resistant strains, FCA‐resistant strains, itraconazole (ITR)‐resistant strains, and sensitive strains. The pathogenicity of C. albicans in descending order was as follows: cross‐resistant strains, VRC‐resistant strains, ITR‐resistant strains, FCA‐resistant strains, and sensitive strains. With the increase of RIT concentrations, the Saps activity was gradually inhibited. Drug sensitivity results showed that there was no synergistic effect between RIT and FCA. Additionally, no gene mutation sites were found in SAP2 sequencing, and 17 synonymous mutations and 6 missense mutations occurred in ERG11 sequencing. Finally, the expression of SAP2 and ERG11 was significantly higher in the resistant strains compared with the sensitive strains, and there was a positive liner correlation between SAP2 and ERG11 messenger RNA expression (r = .6655, p < .001). CONCLUSION: These findings may help to improve our understanding of azole‐resistant mechanisms of C. albicans and provide a novel direction for clinical therapeutics of C. albicans infection. John Wiley and Sons Inc. 2021-05-05 /pmc/articles/PMC8342201/ /pubmed/33951330 http://dx.doi.org/10.1002/iid3.415 Text en © 2021 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Feng, Wenli Yang, Jing Ma, Yan Xi, Zhiqin Zhao, Xiaoqin Zhao, Xiaoxia Zhao, Min The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11 |
title | The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11
|
title_full | The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11
|
title_fullStr | The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11
|
title_full_unstemmed | The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11
|
title_short | The effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of Candida albicans as well as regulatory role of SAP2 and ERG11
|
title_sort | effects of secreted aspartyl proteinase inhibitor ritonavir on azoles‐resistant strains of candida albicans as well as regulatory role of sap2 and erg11 |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342201/ https://www.ncbi.nlm.nih.gov/pubmed/33951330 http://dx.doi.org/10.1002/iid3.415 |
work_keys_str_mv | AT fengwenli theeffectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT yangjing theeffectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT mayan theeffectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT xizhiqin theeffectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT zhaoxiaoqin theeffectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT zhaoxiaoxia theeffectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT zhaomin theeffectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT fengwenli effectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT yangjing effectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT mayan effectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT xizhiqin effectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT zhaoxiaoqin effectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT zhaoxiaoxia effectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 AT zhaomin effectsofsecretedaspartylproteinaseinhibitorritonavironazolesresistantstrainsofcandidaalbicansaswellasregulatoryroleofsap2anderg11 |