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The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species

The brucellae are facultative intracellular bacteria with a cell envelope rich in phosphatidylcholine (PC). PC is abundant in eukaryotes but rare in prokaryotes, and it has been proposed that Brucella uses PC to mimic eukaryotic-like features and avoid innate immune responses in the host. Two PC syn...

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Autores principales: Aragón-Aranda, Beatriz, Palacios-Chaves, Leyre, Salvador-Bescós, Miriam, de Miguel, María Jesús, Muñoz, Pilar M., Vences-Guzmán, Miguel Ángel, Zúñiga-Ripa, Amaia, Lázaro-Antón, Leticia, Sohlenkamp, Christian, Moriyón, Ignacio, Iriarte, Maite, Conde-Álvarez, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371380/
https://www.ncbi.nlm.nih.gov/pubmed/34421831
http://dx.doi.org/10.3389/fmicb.2021.614243
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author Aragón-Aranda, Beatriz
Palacios-Chaves, Leyre
Salvador-Bescós, Miriam
de Miguel, María Jesús
Muñoz, Pilar M.
Vences-Guzmán, Miguel Ángel
Zúñiga-Ripa, Amaia
Lázaro-Antón, Leticia
Sohlenkamp, Christian
Moriyón, Ignacio
Iriarte, Maite
Conde-Álvarez, Raquel
author_facet Aragón-Aranda, Beatriz
Palacios-Chaves, Leyre
Salvador-Bescós, Miriam
de Miguel, María Jesús
Muñoz, Pilar M.
Vences-Guzmán, Miguel Ángel
Zúñiga-Ripa, Amaia
Lázaro-Antón, Leticia
Sohlenkamp, Christian
Moriyón, Ignacio
Iriarte, Maite
Conde-Álvarez, Raquel
author_sort Aragón-Aranda, Beatriz
collection PubMed
description The brucellae are facultative intracellular bacteria with a cell envelope rich in phosphatidylcholine (PC). PC is abundant in eukaryotes but rare in prokaryotes, and it has been proposed that Brucella uses PC to mimic eukaryotic-like features and avoid innate immune responses in the host. Two PC synthesis pathways are known in prokaryotes: the PmtA-catalyzed trimethylation of phosphatidylethanolamine and the direct linkage of choline to CDP-diacylglycerol catalyzed by the PC synthase Pcs. Previous studies have reported that B. abortus and B. melitensis possess non-functional PmtAs and that PC is synthesized exclusively via Pcs in these strains. A putative choline transporter ChoXWV has also been linked to PC synthesis in B. abortus. Here, we report that Pcs and Pmt pathways are active in B. suis biovar 2 and that a bioinformatics analysis of Brucella genomes suggests that PmtA is only inactivated in B. abortus and B. melitensis strains. We also show that ChoXWV is active in B. suis biovar 2 and conserved in all brucellae except B. canis and B. inopinata. Unexpectedly, the experimentally verified ChoXWV dysfunction in B. canis did not abrogate PC synthesis in a PmtA-deficient mutant, which suggests the presence of an unknown mechanism for obtaining choline for the Pcs pathway in Brucella. We also found that ChoXWV dysfunction did not cause attenuation in B. suis biovar 2. The results of these studies are discussed with respect to the proposed role of PC in Brucella virulence and how differential use of the Pmt and Pcs pathways may influence the interactions of these bacteria with their mammalian hosts.
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spelling pubmed-83713802021-08-19 The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species Aragón-Aranda, Beatriz Palacios-Chaves, Leyre Salvador-Bescós, Miriam de Miguel, María Jesús Muñoz, Pilar M. Vences-Guzmán, Miguel Ángel Zúñiga-Ripa, Amaia Lázaro-Antón, Leticia Sohlenkamp, Christian Moriyón, Ignacio Iriarte, Maite Conde-Álvarez, Raquel Front Microbiol Microbiology The brucellae are facultative intracellular bacteria with a cell envelope rich in phosphatidylcholine (PC). PC is abundant in eukaryotes but rare in prokaryotes, and it has been proposed that Brucella uses PC to mimic eukaryotic-like features and avoid innate immune responses in the host. Two PC synthesis pathways are known in prokaryotes: the PmtA-catalyzed trimethylation of phosphatidylethanolamine and the direct linkage of choline to CDP-diacylglycerol catalyzed by the PC synthase Pcs. Previous studies have reported that B. abortus and B. melitensis possess non-functional PmtAs and that PC is synthesized exclusively via Pcs in these strains. A putative choline transporter ChoXWV has also been linked to PC synthesis in B. abortus. Here, we report that Pcs and Pmt pathways are active in B. suis biovar 2 and that a bioinformatics analysis of Brucella genomes suggests that PmtA is only inactivated in B. abortus and B. melitensis strains. We also show that ChoXWV is active in B. suis biovar 2 and conserved in all brucellae except B. canis and B. inopinata. Unexpectedly, the experimentally verified ChoXWV dysfunction in B. canis did not abrogate PC synthesis in a PmtA-deficient mutant, which suggests the presence of an unknown mechanism for obtaining choline for the Pcs pathway in Brucella. We also found that ChoXWV dysfunction did not cause attenuation in B. suis biovar 2. The results of these studies are discussed with respect to the proposed role of PC in Brucella virulence and how differential use of the Pmt and Pcs pathways may influence the interactions of these bacteria with their mammalian hosts. Frontiers Media S.A. 2021-08-04 /pmc/articles/PMC8371380/ /pubmed/34421831 http://dx.doi.org/10.3389/fmicb.2021.614243 Text en Copyright © 2021 Aragón-Aranda, Palacios-Chaves, Salvador-Bescós, de Miguel, Muñoz, Vences-Guzmán, Zúñiga-Ripa, Lázaro-Antón, Sohlenkamp, Moriyón, Iriarte and Conde-Álvarez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Aragón-Aranda, Beatriz
Palacios-Chaves, Leyre
Salvador-Bescós, Miriam
de Miguel, María Jesús
Muñoz, Pilar M.
Vences-Guzmán, Miguel Ángel
Zúñiga-Ripa, Amaia
Lázaro-Antón, Leticia
Sohlenkamp, Christian
Moriyón, Ignacio
Iriarte, Maite
Conde-Álvarez, Raquel
The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species
title The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species
title_full The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species
title_fullStr The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species
title_full_unstemmed The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species
title_short The Phospholipid N-Methyltransferase and Phosphatidylcholine Synthase Pathways and the ChoXWV Choline Uptake System Involved in Phosphatidylcholine Synthesis Are Widely Conserved in Most, but Not All Brucella Species
title_sort phospholipid n-methyltransferase and phosphatidylcholine synthase pathways and the choxwv choline uptake system involved in phosphatidylcholine synthesis are widely conserved in most, but not all brucella species
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371380/
https://www.ncbi.nlm.nih.gov/pubmed/34421831
http://dx.doi.org/10.3389/fmicb.2021.614243
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