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1.
FEMS Immunol Med Microbiol ; 62(2): 148-56, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21348900

ABSTRACT

The human respiratory tract pathogen Chlamydia pneumoniae AR39 is naturally infected by the bacteriophage ϕCPAR39. The phage genome encodes six ORFs, [ORF8, ORF4, ORF5, and viral protein (VP) 1, VP2 and VP3]. To study the growth of the phage, antibodies were generated to VP1 and used to investigate the ϕCPAR39 infection. Using immunofluorescence laser confocal microscopy and two-dimensional gel electrophoresis, we investigated the ϕCPAR39 infection of C. pneumoniae AR39. It was observed that ϕCPAR39 infection differentially suppressed the C. pneumoniae protein synthesis as the polymorphic membrane protein 10 and the secreted chlamydial protein Cpn0796 was hardly expressed while the secreted chlamydial protein Cpaf was expressed, but not secreted. The inclusion membrane protein, IncA, was demonstrated to surround the phage-infected abnormal reticulate bodies (RB) as well as being located in the inclusion membrane. As IncA is secreted by the type 3 secretion (T3S) system, it is likely that the T3S is disrupted in the phage-infected chlamydiae such that it accumulates around the infected RB.


Subject(s)
Bacteriophages/growth & development , Chlamydophila pneumoniae/virology , Inclusion Bodies/ultrastructure , Inclusion Bodies/virology , Bacterial Proteins/analysis , Electrophoresis, Gel, Two-Dimensional , Microscopy, Confocal , Proteome/analysis
2.
FEMS Microbiol Lett ; 273(1): 45-9, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17559388

ABSTRACT

The Chlamydia pneumoniae bacteriophage was first identified in isolate AR-39. Its relevance for chlamydial biology and pathogenicity remains unknown. In this study, a collection of 36 C. pneumoniae isolates was screened and the phage was detected in eight. As the positive isolates differed by several polymorphisms, they presumably belonged to different genetic lineages. It was investigated whether different genotypes of the phage also existed and whether they could be assigned to chlamydial genotypes as evidence of coevolution. Sequencing of >3000 bp of the 4524 bp phage genome revealed complete identity to the published sequences. Thus, it was hypothesized that the genetic conservation was related to easy transmissibility of the phage between C. pneumoniae isolates. Cocultivation of phage positive and negative isolates followed by cloning and identification of different C. pneumoniae genotypes demonstrated for the first time transmissibility of the bacteriophage from one isolate to the other. These observations indicate that the phage is capable of infecting C. pneumoniae isolates of different genetic backgrounds and suggest that all C. pneumoniae strains might be susceptible. The successful in vitro infection of C. pneumoniae with the phage provides the basis for studying its pathogenetic relevance in isolates of identical genetic background and provides a potential tool for genetic manipulation of C. pneumoniae.


Subject(s)
Bacteriophages/growth & development , Bacteriophages/isolation & purification , Chlamydophila pneumoniae/virology , Bacteriophages/classification , Bacteriophages/genetics , DNA, Bacterial/genetics , DNA, Viral/genetics , Genotype , HeLa Cells , Humans , Polymerase Chain Reaction , Polymorphism, Genetic , Sequence Analysis, DNA
3.
J Clin Microbiol ; 40(11): 4010-4, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12409367

ABSTRACT

Recent whole-genome analysis has demonstrated limited genetic variation in Chlamydia pneumoniae, with one strain (AR39) containing a 4,524 nucleotide single-stranded DNA bacteriophage, PhiCpn1. Using PCR, reverse transcription (RT)-PCR, and Western blotting, we confirmed the presence and functional expression of PhiCpn1 in C. pneumoniae strain AR39 and its absence in strain CWL029. Six additional epidemiologically distinct clinical isolates of C. pneumoniae also did not contain PhiCpn1. We generated recombinant viral protein 1 (Vp1) from PhiCpn1 in Escherichia coli and showed that Vp1 antigen is highly immunogenic in mice and that murine antisera readily recognize native Vp1 from C. pneumoniae strain AR39 elementary bodies (EB). We developed an enzyme-linked immunosorbent assay (ELISA) to measure antibodies to recombinant Vp1 in human sera collected from 32 patients with abdominal aortic aneurysm (AAA) and 40 controls. Among the 72 subjects, 61 had C. pneumoniae EB antibodies shown by ELISA. Antibodies to Vp1 were found in 39 of the 61 (64%) seropositive individuals and were significantly correlated with AAA (adjusted odds ratio, 13.9; 95% confidence interval, 1.1 to 175). Our studies indicate that phage-containing strains of C. pneumoniae are uncommonly found by isolation but may commonly infect individuals with vascular disease.


Subject(s)
Antibodies, Viral/blood , Bacteriophages/genetics , Chlamydophila pneumoniae/virology , DNA-Binding Proteins/genetics , DNA-Binding Proteins/immunology , Transcription Factors/genetics , Transcription Factors/immunology , Animals , Antibodies, Bacterial/blood , Aortic Aneurysm, Abdominal/microbiology , Aortic Aneurysm, Abdominal/virology , Bacteriophages/immunology , Chlamydophila Infections/microbiology , Chlamydophila pneumoniae/classification , Chlamydophila pneumoniae/immunology , DNA-Binding Proteins/isolation & purification , Enzyme-Linked Immunosorbent Assay , Humans , Mice , Mice, Inbred BALB C , Plant Proteins , Polymerase Chain Reaction , Recombinant Proteins/immunology , Sensitivity and Specificity , Seroepidemiologic Studies , Trans-Activators , Transcription Factors/isolation & purification
4.
Microbiology (Reading) ; 146 ( Pt 7): 1651-1660, 2000 Jul.
Article in English | MEDLINE | ID: mdl-10878129

ABSTRACT

The authors report the isolation and molecular characterization of a bacteriophage, φCPG1, which infects CHLAMYDIA: psittaci strain Guinea pig Inclusion Conjunctivitis. Purified virion preparations contained isometric particles of 25 nm diameter, superficially similar to spike-less members of the φX174 family of bacteriophages. The single-stranded circular DNA genome of φCPG1 included five large ORFs, which were similar to ORFs in the genome of a previously described CHLAMYDIA: bacteriophage (Chp1) that infects avian C. psittaci. Three of the ORFs encoded polypeptides that were similar to those in a phage infecting the mollicute Spiroplasma melliferum, a pathogen of honeybees. Lesser sequence similarities were seen between two ORF products and the major capsid protein of the φX174 coliphage family and proteins mediating rolling circle replication initiation in phages, phagemids and plasmids. Phage φCPG1 is the second member of the genus CHLAMYDIAMICROVIRUS:, the first to infect a member of a CHLAMYDIA: species infecting mammals. Similarity searches of the nucleotide sequence further revealed a highly conserved (75% identity) 375 base sequence integrated into the genome of the human pathogen Chlamydia pneumoniae. This genomic segment encodes a truncated 113 residue polypeptide, the sequence of which is 72% identical to the amino-terminal end of the putative replication initiation protein of φCPG1. This finding suggests that C. pneumoniae has been infected by a phage related to φCPG1 and that infection resulted in integration of some of the phage genome into the C. pneumoniae genome.


Subject(s)
Chlamydophila psittaci/virology , Conjunctivitis, Inclusion/microbiology , Genome, Viral , Microvirus/genetics , Amino Acid Sequence , Animals , Base Sequence , Capsid/chemistry , Capsid/genetics , Chlamydophila pneumoniae/virology , DNA, Bacterial/genetics , DNA, Viral/genetics , Guinea Pigs , HeLa Cells , Humans , Microscopy, Electron , Microvirus/chemistry , Microvirus/ultrastructure , Molecular Sequence Data , Molecular Weight , Open Reading Frames , Sequence Alignment , Virus Integration
5.
Nucleic Acids Res ; 28(6): 1397-406, 2000 Mar 15.
Article in English | MEDLINE | ID: mdl-10684935

ABSTRACT

The genome sequences of Chlamydia trachomatis mouse pneumonitis (MoPn) strain Nigg (1 069 412 nt) and Chlamydia pneumoniae strain AR39 (1 229 853 nt) were determined using a random shotgun strategy. The MoPn genome exhibited a general conservation of gene order and content with the previously sequenced C.trachomatis serovar D. Differences between C.trachomatis strains were focused on an approximately 50 kb 'plasticity zone' near the termination origins. In this region MoPn contained three copies of a novel gene encoding a >3000 amino acid toxin homologous to a predicted toxin from Escherichia coli O157:H7 but had apparently lost the tryptophan biosyntheis genes found in serovar D in this region. The C. pneumoniae AR39 chromosome was >99.9% identical to the previously sequenced C.pneumoniae CWL029 genome, however, comparative analysis identified an invertible DNA segment upstream of the uridine kinase gene which was in different orientations in the two genomes. AR39 also contained a novel 4524 nt circular single-stranded (ss)DNA bacteriophage, the first time a virus has been reported infecting C. pneumoniae. Although the chlamydial genomes were highly conserved, there were intriguing differences in key nucleotide salvage pathways: C.pneumoniae has a uridine kinase gene for dUTP production, MoPn has a uracil phosphororibosyl transferase, while C.trachomatis serovar D contains neither gene. Chromosomal comparison revealed that there had been multiple large inversion events since the species divergence of C.trachomatis and C.pneumoniae, apparently oriented around the axis of the origin of replication and the termination region. The striking synteny of the Chlamydia genomes and prevalence of tandemly duplicated genes are evidence of minimal chromosome rearrangement and foreign gene uptake, presumably owing to the ecological isolation of the obligate intracellular parasites. In the absence of genetic analysis, comparative genomics will continue to provide insight into the virulence mechanisms of these important human pathogens.


Subject(s)
Chlamydia trachomatis/genetics , Chlamydophila pneumoniae/genetics , Genome, Bacterial , Animals , Bacterial Proteins/genetics , Bacteriophages/genetics , Base Sequence , Chlamydia Infections/microbiology , Chlamydia trachomatis/enzymology , Chlamydia trachomatis/metabolism , Chlamydia trachomatis/pathogenicity , Chlamydophila pneumoniae/enzymology , Chlamydophila pneumoniae/pathogenicity , Chlamydophila pneumoniae/virology , Chromosome Inversion , Conserved Sequence/genetics , Evolution, Molecular , Genes, Bacterial/genetics , Genes, Duplicate/genetics , Humans , Mice/microbiology , Molecular Sequence Data , Nucleotides/metabolism , Physical Chromosome Mapping , Recombination, Genetic/genetics , Replication Origin/genetics
6.
Microb Comp Genomics ; 5(4): 223-31, 2000.
Article in English | MEDLINE | ID: mdl-11471835

ABSTRACT

Three recently discovered ssDNA Chlamydia-infecting microviruses, phiCPG1, phiAR39, and Chp2, were compared with the previously characterized phage from avian C. psittaci, Chp1. Although the four bacteriophages share an identical arrangement of their five main genes, Chpl has diverged significantly in its nucleotide and protein sequences from the other three, which form a closely related group. The VP1 major viral capsid proteins of phiCPG1 and phiAR39 (from guinea pig-infecting C. psittaci and C. pneumoniae, respectively) are almost identical. However, VP1 of ovine C. psittaci phage Chp2 shows a high rate of nucleotide sequence change localized to a region encoding the "IN5" loop of the protein, thought to be a potential receptor-binding site. Phylogenetic analysis suggests that the ORF4 replication initiation protein is evolving faster than the other phage proteins. phiCPG1, phiAR39, and Chp2 are closely related to an ORF4 homolog inserted in the C. pneumoniae chromosome. This sequence analysis opens the way toward understanding the host-range and evolutionary history of these phages.


Subject(s)
Capsid/genetics , Chlamydia/virology , DNA-Binding Proteins , Genome, Viral , Microvirus/classification , Receptors, Virus/metabolism , Amino Acid Sequence , Animals , Base Sequence , Binding Sites , Birds/microbiology , Capsid/chemistry , Capsid/metabolism , Chlamydophila pneumoniae/virology , Chlamydophila psittaci/virology , DNA Helicases/genetics , DNA, Single-Stranded/genetics , DNA, Viral/genetics , Evolution, Molecular , Mammals/microbiology , Microvirus/genetics , Microvirus/isolation & purification , Open Reading Frames , Phylogeny , Protein Conformation , Sequence Alignment , Sequence Homology, Amino Acid , Species Specificity , Trans-Activators/genetics
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