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1.
BMC Microbiol ; 12: 98, 2012 Jun 06.
Article in English | MEDLINE | ID: mdl-22672506

ABSTRACT

BACKGROUND: Herbaspirillum rubrisubalbicans was first identified as a bacterial plant pathogen, causing the mottled stripe disease in sugarcane. H. rubrisubalbicans can also associate with various plants of economic interest in a non pathogenic manner. RESULTS: A 21 kb DNA region of the H. rubrisubalbicans genome contains a cluster of 26 hrp/hrc genes encoding for the type three secretion system (T3SS) proteins. To investigate the contribution of T3SS to the plant-bacterial interaction process we generated mutant strains of H. rubrisubalbicans M1 carrying a Tn5 insertion in both the hrcN and hrpE genes. H. rubrisulbalbicans hrpE and hrcN mutant strains of the T3SS system failed to cause the mottled stripe disease in the sugarcane susceptible variety B-4362. These mutant strains also did not produce lesions on Vigna unguiculata leaves. Oryza sativa and Zea mays colonization experiments showed that mutations in hrpE and hrcN genes reduced the capacity of H. rubrisulbalbicans to colonize these plants, suggesting that hrpE and hrcN genes are involved in the endophytic colonization. CONCLUSIONS: Our results indicate that the T3SS of H. rubrisubalbicans is necessary for the development of the mottled stripe disease and endophytic colonization of rice.


Subject(s)
Bacterial Secretion Systems/genetics , Endophytes/pathogenicity , Herbaspirillum/pathogenicity , Host-Pathogen Interactions , Membrane Transport Proteins/genetics , Plant Diseases/microbiology , Poaceae/microbiology , DNA Transposable Elements , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Endophytes/genetics , Gene Deletion , Herbaspirillum/genetics , Molecular Sequence Data , Multigene Family , Mutagenesis, Insertional , Sequence Analysis, DNA , Virulence Factors/genetics
2.
PLoS Genet ; 7(5): e1002064, 2011 May.
Article in English | MEDLINE | ID: mdl-21589895

ABSTRACT

The molecular mechanisms of plant recognition, colonization, and nutrient exchange between diazotrophic endophytes and plants are scarcely known. Herbaspirillum seropedicae is an endophytic bacterium capable of colonizing intercellular spaces of grasses such as rice and sugar cane. The genome of H. seropedicae strain SmR1 was sequenced and annotated by The Paraná State Genome Programme--GENOPAR. The genome is composed of a circular chromosome of 5,513,887 bp and contains a total of 4,804 genes. The genome sequence revealed that H. seropedicae is a highly versatile microorganism with capacity to metabolize a wide range of carbon and nitrogen sources and with possession of four distinct terminal oxidases. The genome contains a multitude of protein secretion systems, including type I, type II, type III, type V, and type VI secretion systems, and type IV pili, suggesting a high potential to interact with host plants. H. seropedicae is able to synthesize indole acetic acid as reflected by the four IAA biosynthetic pathways present. A gene coding for ACC deaminase, which may be involved in modulating the associated plant ethylene-signaling pathway, is also present. Genes for hemagglutinins/hemolysins/adhesins were found and may play a role in plant cell surface adhesion. These features may endow H. seropedicae with the ability to establish an endophytic life-style in a large number of plant species.


Subject(s)
Genome, Plant , Herbaspirillum/genetics , Chromosomes, Plant , Herbaspirillum/metabolism , Host-Pathogen Interactions , Nitrogen Fixation , Osmotic Pressure , Plant Proteins/genetics , Plant Proteins/metabolism
3.
Vaccine ; 29(21): 3729-30, 2011 May 12.
Article in English | MEDLINE | ID: mdl-21414381

ABSTRACT

Group B streptococcal (GBS) capsular polysaccharide (CPS)-based conjugate vaccine, which includes types Ia, Ib, II, III, and V, could potentially prevent neonatal, pediatric, adult, and pregnancy-associated diseases. However, since GBS CPS types included in that vaccine are prevalent serotypes found in North America and Europe, it may not provide the necessary protection for individuals in countries in which other capsular types have been found.


Subject(s)
Polysaccharides, Bacterial/immunology , Streptococcal Infections/prevention & control , Streptococcal Vaccines/immunology , Streptococcus agalactiae/classification , Female , Humans , Immunization , Pregnancy , Prevalence , Serotyping , Streptococcal Infections/epidemiology , Streptococcal Vaccines/administration & dosage , Streptococcus agalactiae/immunology , Vaccines, Conjugate/administration & dosage , Vaccines, Conjugate/immunology
4.
J Clin Microbiol ; 48(12): 4397-403, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20881175

ABSTRACT

One-hundred sixty-eight group B streptococcal (GBS) isolates from a Brazilian hospital were phenotypically and genotypically characterized. Isolates were recovered from human sources from April 2006 to May 2008 and classified as either invasive, noninvasive, or colonizing isolates. Classical methods for serotyping and antibiotic resistance profiling were employed. Clonal groups were also defined by pulsed-field gel electrophoresis (PFGE). Results showed that susceptibility to beta-lactam antimicrobials was predominant among the isolates. Only 4.7% were resistant to erythromycin and clindamycin. The erm(B) gene was widely detected in our GBS isolates, according to our phenotypic results (constitutive macrolide-lincosamide-streptogramin B [cMLSB] resistance phenotype), and the erm(A) gene was also detected in some isolates. MLSB resistance was restricted to strains isolated from patients with noninvasive infections and carriers. Serotype Ia was predominant (38.1%), serotype IV isolates were found at a high frequency (13.1%), and few isolates of serotype III were identified (3%). Pulsed-field gel electrophoresis results revealed a variety of types, reflecting the substantial genetic diversity among GBS strains, although a great number of isolates could be clustered into two major groups with a high degree of genetic relatedness. Three main PFGE clonal groups were found, and isolates sharing the same PFGE type were grouped into different serotypes. Furthermore, in a few cases, isolates from the same patients and possessing the same PFGE type were of different serotypes. These findings could be related to the occurrence of capsular switching by horizontal transfer of capsular genes.


Subject(s)
Streptococcal Infections/microbiology , Streptococcus agalactiae/classification , Streptococcus agalactiae/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/pharmacology , Bacterial Typing Techniques , Brazil , Cluster Analysis , Drug Resistance, Bacterial , Electrophoresis, Gel, Pulsed-Field , Female , Genotype , Hospitals , Humans , Infant, Newborn , Male , Microbial Sensitivity Tests , Middle Aged , Molecular Epidemiology , Molecular Typing , Phenotype , Pregnancy , Serotyping , Streptococcus agalactiae/isolation & purification , Young Adult
5.
J Bacteriol ; 187(16): 5568-77, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16077101

ABSTRACT

This work reports the results of analyses of three complete mycoplasma genomes, a pathogenic (7448) and a nonpathogenic (J) strain of the swine pathogen Mycoplasma hyopneumoniae and a strain of the avian pathogen Mycoplasma synoviae; the genome sizes of the three strains were 920,079 bp, 897,405 bp, and 799,476 bp, respectively. These genomes were compared with other sequenced mycoplasma genomes reported in the literature to examine several aspects of mycoplasma evolution. Strain-specific regions, including integrative and conjugal elements, and genome rearrangements and alterations in adhesin sequences were observed in the M. hyopneumoniae strains, and all of these were potentially related to pathogenicity. Genomic comparisons revealed that reduction in genome size implied loss of redundant metabolic pathways, with maintenance of alternative routes in different species. Horizontal gene transfer was consistently observed between M. synoviae and Mycoplasma gallisepticum. Our analyses indicated a likely transfer event of hemagglutinin-coding DNA sequences from M. gallisepticum to M. synoviae.


Subject(s)
Genome, Bacterial , Mycoplasma Infections/microbiology , Mycoplasma hyopneumoniae/genetics , Mycoplasma synoviae/genetics , Pneumonia of Swine, Mycoplasmal/microbiology , Poultry Diseases/microbiology , Animals , Evolution, Molecular , Gene Rearrangement , Gene Transfer, Horizontal , Genomics , Molecular Sequence Data , Phylogeny , Poultry , Swine
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