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1.
J Bacteriol ; 190(24): 8197-203, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18931122

ABSTRACT

The Brucella cell envelope contains the zwitterionic phospholipids phosphatidylcholine (PC) and phosphatidylethanolamine (PE). Synthesis of PC occurs exclusively via the PC synthase pathway, implying that the pathogen depends on the choline synthesized by the host cell to form PC. Notably, PC is necessary to sustain a chronic infection process, which suggests that the membrane lipid content is relevant for Brucella virulence. In this study we investigated the first step of PE biosynthesis in B. abortus, which is catalyzed by phosphatidylserine synthase (PssA). Disruption of pssA abrogated the synthesis of PE without affecting the growth in rich complex medium. In minimal medium, however, the mutant required choline supplementation for growth, suggesting that at least PE or PC is necessary for Brucella viability. The absence of PE altered cell surface properties, but most importantly, it impaired several virulence traits of B. abortus, such as intracellular survival in both macrophages and HeLa cells, the maturation of the replicative Brucella-containing vacuole, and mouse colonization. These results suggest that membrane phospholipid composition is critical for the interaction of B. abortus with the host cell.


Subject(s)
Brucella abortus/metabolism , Brucella abortus/pathogenicity , Phosphatidylethanolamines/biosynthesis , Animals , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Brucella abortus/genetics , Brucellosis/microbiology , CDPdiacylglycerol-Serine O-Phosphatidyltransferase/genetics , CDPdiacylglycerol-Serine O-Phosphatidyltransferase/metabolism , DNA, Bacterial/genetics , Female , Gene Knockout Techniques , Genes, Bacterial , HeLa Cells , Humans , Macrophages/microbiology , Mice , Mice, Inbred BALB C , Mutation , Phosphatidylcholines/biosynthesis , Plasmids , Virulence
2.
Microbiology (Reading) ; 149(Pt 12): 3461-3471, 2003 Dec.
Article in English | MEDLINE | ID: mdl-14663079

ABSTRACT

Phosphatidylcholine (PC) is the major membrane-forming phospholipid in eukaryotes with important structural and signalling functions. Although many prokaryotes lack PC, it can be found in significant amounts in membranes of rather diverse bacteria. Two pathways for PC biosynthesis are known in bacteria, the methylation pathway and the phosphatidylcholine synthase (PCS) pathway. In the methylation pathway, phosphatidylethanolamine is methylated three times to yield PC, in reactions catalysed by one or several phospholipid N-methyltransferases (PMTs). In the PCS pathway, choline is condensed directly with CDP-diacylglyceride to form PC in a reaction catalysed by PCS. Using cell-free extracts, it was demonstrated that Sinorhizobium meliloti, Agrobacterium tumefaciens, Rhizobium leguminosarum, Bradyrhizobium japonicum, Mesorhizobium loti and Legionella pneumophila have both PMT and PCS activities. In addition, Rhodobacter sphaeroides has PMT activity and Brucella melitensis, Pseudomonas aeruginosa and Borrelia burgdorferi have PCS activities. Genes from M. loti and L. pneumophila encoding a Pmt or a Pcs activity and the genes from P. aeruginosa and Borrelia burgdorferi responsible for Pcs activity have been identified. Based on these functional assignments and on genomic data, one might predict that if bacteria contain PC as a membrane lipid, they usually possess both bacterial pathways for PC biosynthesis. However, important pathogens such as Brucella melitensis, P. aeruginosa and Borrelia burgdorferi seem to be exceptional as they possess only the PCS pathway for PC formation.


Subject(s)
Bacteria/metabolism , Phosphatidylcholines/biosynthesis , Bacteria/genetics , Base Sequence , CDPdiacylglycerol-Serine O-Phosphatidyltransferase/genetics , CDPdiacylglycerol-Serine O-Phosphatidyltransferase/metabolism , DNA, Bacterial/genetics , Diacylglycerol Cholinephosphotransferase/genetics , Diacylglycerol Cholinephosphotransferase/metabolism , Genes, Bacterial , Membrane Lipids/biosynthesis , Methylation , Methyltransferases/genetics , Methyltransferases/metabolism , Open Reading Frames , Phosphatidyl-N-Methylethanolamine N-Methyltransferase , Phylogeny
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