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Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System
BACKGROUND: A mouse brain transmigration assessment (MBTA) was created to investigate the central nervous system (CNS) pathogenesis of cryptococcal meningoencephalitis. METHODOLOGY/PRINCIPAL FINDINGS: Two cryptococcal mutants were identified from a pool of 109 pre-selected mutants that were signatur...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447876/ https://www.ncbi.nlm.nih.gov/pubmed/23028773 http://dx.doi.org/10.1371/journal.pone.0045083 |
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author | Tseng, Hsiang-Kuang Liu, Chang-Pan Price, Michael S. Jong, Ambrose Y. Chang, Jui-Chih Toffaletti, Dena L. Betancourt-Quiroz, Marisol Frazzitta, Aubrey E. Cho, Wen-Long Perfect, John R. |
author_facet | Tseng, Hsiang-Kuang Liu, Chang-Pan Price, Michael S. Jong, Ambrose Y. Chang, Jui-Chih Toffaletti, Dena L. Betancourt-Quiroz, Marisol Frazzitta, Aubrey E. Cho, Wen-Long Perfect, John R. |
author_sort | Tseng, Hsiang-Kuang |
collection | PubMed |
description | BACKGROUND: A mouse brain transmigration assessment (MBTA) was created to investigate the central nervous system (CNS) pathogenesis of cryptococcal meningoencephalitis. METHODOLOGY/PRINCIPAL FINDINGS: Two cryptococcal mutants were identified from a pool of 109 pre-selected mutants that were signature-tagged with the nourseothricin acetyltransferase (NAT) resistance cassette. These two mutants displayed abnormal transmigration into the central nervous system. One mutant displaying decreased transmigration contains a null mutation in the putative FNX1 gene, whereas the other mutant possessing a null mutation in the putative RUB1 gene exhibited increased transmigration into the brain. Two macrophage adhesion-defective mutants in the pool, 12F1 and 3C9, showed reduced phagocytosis by macrophages, but displayed no defects in CNS entry suggesting that transit within macrophages (the “Trojan horse” model of CNS entry) is not the primary mechanism for C. neoformans migration into the CNS in this MBTA. CONCLUSIONS/SIGNIFICANCE: This research design provides a new strategy for genetic impact studies on how Cryptococcus passes through the blood-brain barrier (BBB), and the specific isolated mutants in this assay support a transcellular mechanism of CNS entry. |
format | Online Article Text |
id | pubmed-3447876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34478762012-10-01 Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System Tseng, Hsiang-Kuang Liu, Chang-Pan Price, Michael S. Jong, Ambrose Y. Chang, Jui-Chih Toffaletti, Dena L. Betancourt-Quiroz, Marisol Frazzitta, Aubrey E. Cho, Wen-Long Perfect, John R. PLoS One Research Article BACKGROUND: A mouse brain transmigration assessment (MBTA) was created to investigate the central nervous system (CNS) pathogenesis of cryptococcal meningoencephalitis. METHODOLOGY/PRINCIPAL FINDINGS: Two cryptococcal mutants were identified from a pool of 109 pre-selected mutants that were signature-tagged with the nourseothricin acetyltransferase (NAT) resistance cassette. These two mutants displayed abnormal transmigration into the central nervous system. One mutant displaying decreased transmigration contains a null mutation in the putative FNX1 gene, whereas the other mutant possessing a null mutation in the putative RUB1 gene exhibited increased transmigration into the brain. Two macrophage adhesion-defective mutants in the pool, 12F1 and 3C9, showed reduced phagocytosis by macrophages, but displayed no defects in CNS entry suggesting that transit within macrophages (the “Trojan horse” model of CNS entry) is not the primary mechanism for C. neoformans migration into the CNS in this MBTA. CONCLUSIONS/SIGNIFICANCE: This research design provides a new strategy for genetic impact studies on how Cryptococcus passes through the blood-brain barrier (BBB), and the specific isolated mutants in this assay support a transcellular mechanism of CNS entry. Public Library of Science 2012-09-20 /pmc/articles/PMC3447876/ /pubmed/23028773 http://dx.doi.org/10.1371/journal.pone.0045083 Text en © 2012 Tseng et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tseng, Hsiang-Kuang Liu, Chang-Pan Price, Michael S. Jong, Ambrose Y. Chang, Jui-Chih Toffaletti, Dena L. Betancourt-Quiroz, Marisol Frazzitta, Aubrey E. Cho, Wen-Long Perfect, John R. Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System |
title | Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System |
title_full | Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System |
title_fullStr | Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System |
title_full_unstemmed | Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System |
title_short | Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System |
title_sort | identification of genes from the fungal pathogen cryptococcus neoformans related to transmigration into the central nervous system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3447876/ https://www.ncbi.nlm.nih.gov/pubmed/23028773 http://dx.doi.org/10.1371/journal.pone.0045083 |
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