RESUMO
BACKGROUND: Caulobacter spp. are Gram-negative bacteria that have rarely been found to be pathogenic in humans. CASE DESCRIPTION: This report describes the first case, to our knowledge, of meningitis in an adult patient caused by Caulobacter spp. A 75-year-old man was operated for a glioblastoma with no evident signs of primary infection in the wound site. Eight days after surgery, the patient developed signs and symptoms of meningitis. Caulobacter was then isolated on 3 separate occasions in the patient's cerebrospinal fluid. Thereafter, specific antibiotic therapy began. After 2 weeks of therapy, the patient was discharged with complete resolution of any related symptoms. CONCLUSIONS: Caulobacter spp. can cause adult meningitis even where there is no evidence of surgical site infection.
Assuntos
Neoplasias Encefálicas/cirurgia , Caulobacter/patogenicidade , Glioblastoma/cirurgia , Infecções por Bactérias Gram-Negativas/diagnóstico , Meningites Bacterianas/diagnóstico , Complicações Pós-Operatórias/diagnóstico , Idoso , Caulobacter/efeitos dos fármacos , Líquido Cefalorraquidiano/microbiologia , Infecções por Bactérias Gram-Negativas/tratamento farmacológico , Humanos , Masculino , Meningites Bacterianas/tratamento farmacológico , Meropeném , Testes de Sensibilidade Microbiana , Complicações Pós-Operatórias/tratamento farmacológico , Tienamicinas/uso terapêutico , VirulênciaRESUMO
In the environment, microorganisms are living in diverse communities, which are impacted by the prevailing environmental conditions. Here, we present a study investigating the effect of low pH and elevated uranium concentration on the dynamics of an artificial microbial consortium. The members (Caulobacter sp. OR37, Asinibacterium sp. OR53, Ralstonia sp. OR214 and Rhodanobacter sp. OR444) were isolated from a uranium contaminated and acidic subsurface sediment. In pure culture, Ralstonia sp. OR214 had the highest growth rate at neutral and low pH and only Caulobacter sp. OR37 and Asinibacterium sp. OR53 grew in the presence uranium. The four strains were mixed in equal ratios, incubated at neutral and low pH and in the presence uranium and transferred to fresh medium once per week for 30 weeks. After 30 weeks, Ralstonia sp. OR214 was dominant at low and neutral pH and Caulobacter sp. OR37 and Asinibacterium sp. OR53 were dominant in the presence of uranium. After 12 weeks, the cultures were also transferred to new conditions to access the response of the consortia to changing conditions. The transfers showed an irreversible effect of uranium, but not of low pH on the consortia. Overall, the strains initially tolerant to the respective conditions persisted over time in high abundances in the consortia.
Assuntos
Bacteroidetes/crescimento & desenvolvimento , Caulobacter/crescimento & desenvolvimento , Gammaproteobacteria/crescimento & desenvolvimento , Consórcios Microbianos/efeitos dos fármacos , Ralstonia/crescimento & desenvolvimento , Urânio/farmacologia , Bacteroidetes/efeitos dos fármacos , Bacteroidetes/isolamento & purificação , Caulobacter/efeitos dos fármacos , Caulobacter/isolamento & purificação , Gammaproteobacteria/efeitos dos fármacos , Gammaproteobacteria/isolamento & purificação , Concentração de Íons de Hidrogênio , Ralstonia/efeitos dos fármacos , Ralstonia/isolamento & purificação , TempoRESUMO
Caulobacter crescentus initiates a single round of DNA replication during each cell cycle. Following the initiation of DNA replication, the essential CckA histidine kinase is activated by phosphorylation, which (via the ChpT phosphotransferase) enables the phosphorylation and activation of the CtrA global regulator. CtrA approximately P then blocks the reinitiation of replication while regulating the transcription of a large number of cell cycle-controlled genes. It has been shown that DNA replication serves as a checkpoint for flagellar biosynthesis and cell division and that this checkpoint is mediated by the availability of active CtrA. Because CckA approximately P promotes the activation of CtrA, we addressed the question of what controls the temporal activation of CckA. We found that the initiation of DNA replication is a prerequisite for remodeling the new cell pole, which includes the localization of the DivL protein kinase to that pole and, consequently, the localization, autophosphorylation, and activation of CckA at that pole. Thus, CckA activation is dependent on polar remodeling and a DNA replication initiation checkpoint that is tightly integrated with the polar phospho-signaling cascade governing cell cycle progression.
Assuntos
Caulobacter/citologia , Caulobacter/enzimologia , Ciclo Celular/fisiologia , Replicação do DNA/fisiologia , Proteínas Quinases/metabolismo , Proteínas de Bactérias/metabolismo , Proteínas de Bactérias/fisiologia , Caulobacter/efeitos dos fármacos , Caulobacter/genética , Proteínas de Ligação a DNA/fisiologia , Ativação Enzimática , Regulação Bacteriana da Expressão Gênica/fisiologia , Histidina Quinase , Novobiocina/farmacologia , Transporte Proteico/efeitos dos fármacos , Transporte Proteico/fisiologia , Fatores de Transcrição/fisiologiaRESUMO
As the provision of potable water is critical for successful habitation of the International Space Station (ISS), life support systems were installed in December 2008 to recycle both humidity from the atmosphere and urine to conserve available water in the Station. In-flight pre-consumption testing from the dispensing needle at the Potable Water Dispenser (PWD) indicated that bacterial concentrations exceeded the current ISS specifications of 50 colony-forming units (CFU) ml(-1). Subsequent investigations revealed that a corrugated stainless steel flex hose upstream of the dispensing needle in the PWD was filled with nonsterile water and left at room temperature for more than 1 month before launch. To simulate biofilm formation that was suspected in the flight system, sterile flex hoses were seeded with a consortium of bacterial isolates previously recovered from other ISS water systems, including Ralstonia pickettii, Burkholderia multivorans, Caulobacter vibrioides, and Cupriavidus pauculus. After incubation for 5 days, the hoses were challenged with various chemical disinfectants including hydrogen peroxide (H2O2), colloidal silver, and buffered pH solutions to determine the ability of the disinfectants to decrease and maintain bacterial concentrations below ISS specifications. The disinfection efficacy over time was measured by collecting daily heterotrophic plate counts after exposure to the disinfectants. A single flush with either 6% H2O2 solution or a mixture of 3% H2O2 and 400 ppb colloidal silver effectively reduced the bacterial concentrations to <1 CFU ml(-1) for a period of up to 3 months.
Assuntos
Biofilmes/efeitos dos fármacos , Desinfetantes/farmacologia , Desinfecção/métodos , Peróxido de Hidrogênio/farmacologia , Prata/farmacologia , Astronave , Abastecimento de Água , Biofilmes/crescimento & desenvolvimento , Burkholderia/classificação , Burkholderia/efeitos dos fármacos , Burkholderia/crescimento & desenvolvimento , Caulobacter/classificação , Caulobacter/efeitos dos fármacos , Caulobacter/crescimento & desenvolvimento , Coloides/farmacologia , Contagem de Colônia Microbiana , Contaminação de Equipamentos , Ralstonia pickettii/efeitos dos fármacos , Ralstonia pickettii/crescimento & desenvolvimentoRESUMO
Prodigiosin is a reddish antibiotic pigment that plays an important role in the biocontrol of plant diseases by the bacterium Serratia marcescens. However, its activity is unstable under agricultural conditions; further, it can be degraded by various environmental factors. To examine the effect of epiphytic microbes on the stability of prodigiosin used for biological control processes, we collected a total of 1,280 bacterial isolates from the phylloplane of cyclamen and tomato plants. Approximately 72% of the bacterial strains isolated from the cyclamen plants and 66% of those isolated from the tomato plants grew on minimal agar medium containing 100 microg ml(-1) prodigiosin. Certain isolates obtained from both plant species exhibited prodigiosin-degrading activity. We compared the 16S rRNA gene sequences derived from the isolates with sequences in a database. The comparison revealed that the sequences determined for the prodigiosin-degrading isolates were homologous to those of the genera Pseudomonas, Caulobacter, Rhizobium, Sphingomonas, Janthinobacterium, Novosphingobium, and Rathayibacter. These results indicate that indigenous epiphytic microorganisms may interfere with the interaction between plant pathogens and biocontrol agents by degrading the antibiotics produced by the agents.
Assuntos
Fenômenos Fisiológicos Bacterianos , Cyclamen/microbiologia , Doenças das Plantas/estatística & dados numéricos , Plantas/microbiologia , Prodigiosina/farmacologia , Bactérias/efeitos dos fármacos , Bactérias/crescimento & desenvolvimento , Bactérias/isolamento & purificação , Caulobacter/efeitos dos fármacos , Primers do DNA , DNA Bacteriano/genética , DNA Bacteriano/isolamento & purificação , Doenças das Plantas/imunologia , Pseudomonas/efeitos dos fármacos , Rhizobium/efeitos dos fármacosRESUMO
Growth environments are important metabolic and developmental regulators. Here we demonstrate a growth environment-dependent effect on Caulobacter chromosome segregation of a small-molecule inhibitor of the MreB bacterial actin cytoskeleton. Our results also implicate ParAB as important segregation determinants, suggesting that multiple distinct mechanisms can mediate Caulobacter chromosome segregation and that their relative contributions can be environmentally regulated.
Assuntos
Caulobacter/genética , Segregação de Cromossomos/genética , Cromossomos Bacterianos/genética , Proteínas de Bactérias/genética , Proteínas de Bactérias/fisiologia , Caulobacter/efeitos dos fármacos , Segregação de Cromossomos/efeitos dos fármacos , Tioureia/análogos & derivados , Tioureia/farmacologiaRESUMO
The sequenced chromosome of Caulobacter crescentus CB15 encodes a hypothetical protein that exhibits significant similarity (30 to 35% identical residues) to metallo-beta-lactamases of subclass B3. An allelic variant of this gene (divergent by 3% of its nucleotides) was cloned in Escherichia coli from C. crescentus type strain DSM4727. Expression studies confirmed the metallo-beta-lactamase activity of its product, CAU-1. The enzyme produced in E. coli was purified by two ion-exchange chromatography steps. CAU-1 contains a 29-kDa polypeptide with an alkaline isoelectric pH (> 9), and unlike the L1 enzyme of Stenotrophomonas maltophilia, the native form is monomeric. Kinetic analysis revealed a preferential activity toward penicillins, carbapenems, and narrow-spectrum cephalosporins, while oxyimino cephalosporins were poorly or not hydrolyzed. Affinities for the various beta-lactams were poor overall (K(m) values were always > 100 microM and often > 400 microM). The interaction with divalent ion chelators appeared to occur by a mechanism similar to that prevailing in other members of subclass B3. In C. crescentus, the CAU-1 enzyme is produced independently of beta-lactam exposure and, interestingly, the bla(CAU) determinant is bracketed by three other genes, including two genes encoding enzymes involved in methionine biosynthesis and a gene encoding a putative transcriptional regulator, in an operon-like structure. The CAU-1 enzyme is the first example of a metallo-beta-lactamase in a member of the alpha subdivision of the class Proteobacteria:
Assuntos
Caulobacter/enzimologia , Caulobacter/genética , Cromossomos Bacterianos/genética , Sequência de Aminoácidos , Antibacterianos/farmacologia , Caulobacter/efeitos dos fármacos , Quelantes/farmacologia , Cromatografia em Gel , Clonagem Molecular , DNA Bacteriano/biossíntese , DNA Bacteriano/genética , Cinética , Testes de Sensibilidade Microbiana , Dados de Sequência Molecular , Proteínas Recombinantes/biossíntese , Proteínas Recombinantes/genética , Espectrometria de Massas por Ionização por Electrospray , beta-LactamasRESUMO
Caulobacter crescentus is one of a small number of bacterial species that contain a periplasmic copper-zinc superoxide dismutase (CuZnSOD). A C. crescentus mutant, with the CuZnSOD gene interrupted by a promoterless cat gene, was constructed and characterized to analyze CuZnSOD function. Periplasmic SOD does not protect against oxyradical damage in the cytosol or play a major role in maintaining the integrity of the cell envelope. Studies of the effect of sodium citrate on plating efficiency suggest that CuZnSOD protects a periplasmic or membrane function(s) requiring magnesium or calcium.