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Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin
Acquisition of iron is necessary for the replication of nearly all bacterial pathogens; however, iron of vertebrate hosts is mostly sequestered by heme and bound to hemoglobin within red blood cells. In Bacillus anthracis, the spore-forming agent of anthrax, the mechanisms of iron scavenging from he...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2515342/ https://www.ncbi.nlm.nih.gov/pubmed/18725935 http://dx.doi.org/10.1371/journal.ppat.1000132 |
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author | Maresso, Anthony W. Garufi, Gabriella Schneewind, Olaf |
author_facet | Maresso, Anthony W. Garufi, Gabriella Schneewind, Olaf |
author_sort | Maresso, Anthony W. |
collection | PubMed |
description | Acquisition of iron is necessary for the replication of nearly all bacterial pathogens; however, iron of vertebrate hosts is mostly sequestered by heme and bound to hemoglobin within red blood cells. In Bacillus anthracis, the spore-forming agent of anthrax, the mechanisms of iron scavenging from hemoglobin are unknown. We report here that B. anthracis secretes IsdX1 and IsdX2, two NEAT domain proteins, to remove heme from hemoglobin, thereby retrieving iron for bacterial growth. Unlike other Gram-positive bacteria, which rely on cell wall anchored Isd proteins for heme scavenging, B. anthracis seems to have also evolved NEAT domain proteins in the extracellular milieu and in the bacterial envelope to provide for the passage of heme. |
format | Text |
id | pubmed-2515342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25153422008-08-22 Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin Maresso, Anthony W. Garufi, Gabriella Schneewind, Olaf PLoS Pathog Research Article Acquisition of iron is necessary for the replication of nearly all bacterial pathogens; however, iron of vertebrate hosts is mostly sequestered by heme and bound to hemoglobin within red blood cells. In Bacillus anthracis, the spore-forming agent of anthrax, the mechanisms of iron scavenging from hemoglobin are unknown. We report here that B. anthracis secretes IsdX1 and IsdX2, two NEAT domain proteins, to remove heme from hemoglobin, thereby retrieving iron for bacterial growth. Unlike other Gram-positive bacteria, which rely on cell wall anchored Isd proteins for heme scavenging, B. anthracis seems to have also evolved NEAT domain proteins in the extracellular milieu and in the bacterial envelope to provide for the passage of heme. Public Library of Science 2008-08-22 /pmc/articles/PMC2515342/ /pubmed/18725935 http://dx.doi.org/10.1371/journal.ppat.1000132 Text en Maresso 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 Maresso, Anthony W. Garufi, Gabriella Schneewind, Olaf Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin |
title |
Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin |
title_full |
Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin |
title_fullStr |
Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin |
title_full_unstemmed |
Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin |
title_short |
Bacillus anthracis Secretes Proteins That Mediate Heme Acquisition from Hemoglobin |
title_sort | bacillus anthracis secretes proteins that mediate heme acquisition from hemoglobin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2515342/ https://www.ncbi.nlm.nih.gov/pubmed/18725935 http://dx.doi.org/10.1371/journal.ppat.1000132 |
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