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Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load
BACKGROUND: Many studies in the past have evaluated the role of immune system boosters in the treatment of leishmania major infection. Protein A (PA) is one of the structural components in peptidoglycan cell wall of gram-negative bacteria such as staphylococcus aurous which functions as a stimulator...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186034/ https://www.ncbi.nlm.nih.gov/pubmed/37200745 http://dx.doi.org/10.4103/abr.abr_291_20 |
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author | Tavalaei, Zahra Zeinalian, Mehrdad Khanahmad, Hossein Hejazi, Hossein |
author_facet | Tavalaei, Zahra Zeinalian, Mehrdad Khanahmad, Hossein Hejazi, Hossein |
author_sort | Tavalaei, Zahra |
collection | PubMed |
description | BACKGROUND: Many studies in the past have evaluated the role of immune system boosters in the treatment of leishmania major infection. Protein A (PA) is one of the structural components in peptidoglycan cell wall of gram-negative bacteria such as staphylococcus aurous which functions as a stimulator in the cellular immune system. The present study aims to evaluate the anti-inflammatory effect of PA on the recovery of leishmania major infection. MATERIALS AND METHODS: This study was conducted on 24 female Balb/c-infected mice. The experimental group received PA at a dose of 60 mg/kg for four weeks. There was no intervention for the negative control group; the third group received the solvent of PA and sterile H2O; and the positive control group received Amphotericin B at a dose of 1 mg/kg body weight. At the end of the treatment period, a real-time polymerase chain reaction (PCR) assay was performed to determine parasitic burden, and the size of the lesions was measured by caliper with an accuracy of 0.01 mm. RESULTS: Results showed that PA did slightly decrease the wound spread and growth but not to an extent that can be considered statistically significant. Also, differences in cycle threshold (Ct) values between the treated group and the untreated group was not impressive. CONCLUSIONS: Although findings showed that PA isn't such a good candidate for leishmania treatment, it may still be suitable for therapies that use multiple drugs in combination to speed up the healing of leishmaniosis, an issue that merits evaluation in future studies. |
format | Online Article Text |
id | pubmed-10186034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-101860342023-05-17 Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load Tavalaei, Zahra Zeinalian, Mehrdad Khanahmad, Hossein Hejazi, Hossein Adv Biomed Res Original Article BACKGROUND: Many studies in the past have evaluated the role of immune system boosters in the treatment of leishmania major infection. Protein A (PA) is one of the structural components in peptidoglycan cell wall of gram-negative bacteria such as staphylococcus aurous which functions as a stimulator in the cellular immune system. The present study aims to evaluate the anti-inflammatory effect of PA on the recovery of leishmania major infection. MATERIALS AND METHODS: This study was conducted on 24 female Balb/c-infected mice. The experimental group received PA at a dose of 60 mg/kg for four weeks. There was no intervention for the negative control group; the third group received the solvent of PA and sterile H2O; and the positive control group received Amphotericin B at a dose of 1 mg/kg body weight. At the end of the treatment period, a real-time polymerase chain reaction (PCR) assay was performed to determine parasitic burden, and the size of the lesions was measured by caliper with an accuracy of 0.01 mm. RESULTS: Results showed that PA did slightly decrease the wound spread and growth but not to an extent that can be considered statistically significant. Also, differences in cycle threshold (Ct) values between the treated group and the untreated group was not impressive. CONCLUSIONS: Although findings showed that PA isn't such a good candidate for leishmania treatment, it may still be suitable for therapies that use multiple drugs in combination to speed up the healing of leishmaniosis, an issue that merits evaluation in future studies. Wolters Kluwer - Medknow 2023-03-21 /pmc/articles/PMC10186034/ /pubmed/37200745 http://dx.doi.org/10.4103/abr.abr_291_20 Text en Copyright: © 2023 Advanced Biomedical Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Tavalaei, Zahra Zeinalian, Mehrdad Khanahmad, Hossein Hejazi, Hossein Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load |
title | Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load |
title_full | Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load |
title_fullStr | Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load |
title_full_unstemmed | Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load |
title_short | Anti-leishmaniasis Effect of Staphylococcus Aureus Protein A on the Size of the Lesion and Parasitic Load |
title_sort | anti-leishmaniasis effect of staphylococcus aureus protein a on the size of the lesion and parasitic load |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186034/ https://www.ncbi.nlm.nih.gov/pubmed/37200745 http://dx.doi.org/10.4103/abr.abr_291_20 |
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