RESUMEN
Streptococcus anginosus (S. anginosus) was enriched in the gastric mucosa of patients with gastric cancer (GC). Here, we show that S. anginosus colonized the mouse stomach and induced acute gastritis. S. anginosus infection spontaneously induced progressive chronic gastritis, parietal cell atrophy, mucinous metaplasia, and dysplasia in conventional mice, and the findings were confirmed in germ-free mice. In addition, S. anginosus accelerated GC progression in carcinogen-induced gastric tumorigenesis and YTN16 GC cell allografts. Consistently, S. anginosus disrupted gastric barrier function, promoted cell proliferation, and inhibited apoptosis. Mechanistically, we identified an S. anginosus surface protein, TMPC, that interacts with Annexin A2 (ANXA2) receptor on gastric epithelial cells. Interaction of TMPC with ANXA2 mediated attachment and colonization of S. anginosus and induced mitogen-activated protein kinase (MAPK) activation. ANXA2 knockout abrogated the induction of MAPK by S. anginosus. Thus, this study reveals S. anginosus as a pathogen that promotes gastric tumorigenesis via direct interactions with gastric epithelial cells in the TMPC-ANXA2-MAPK axis.
Asunto(s)
Gastritis , Neoplasias Gástricas , Infecciones Estreptocócicas , Streptococcus anginosus , Animales , Humanos , Ratones , Atrofia/patología , Carcinogénesis , Transformación Celular Neoplásica , Mucosa Gástrica , Gastritis/patología , Inflamación/patología , Proteínas Quinasas Activadas por Mitógenos , Neoplasias Gástricas/microbiología , Neoplasias Gástricas/patología , Streptococcus anginosus/fisiología , Infecciones Estreptocócicas/patologíaRESUMEN
Surgery for prosthetic valve endocarditis in the mitral valve position is still challenging for surgeons. Reconstruction of the mitral annulus is useful for patients with a mitral annulus disputed by infection. Here, we report a redo mitral valve replacement using a collar-reinforced tissue valve, which was inserted into a mitral annulus reconstructed with a bovine patch. Though the preoperative blood culture detected Streptococcus anginosus, the intraoperative culture detected methicillin-resistant coagulase-negative staphylococci (MRCNS). MRCNS is rarely detected because of its indolent nature.
Asunto(s)
Antibacterianos/uso terapéutico , Endocarditis Bacteriana/terapia , Implantación de Prótesis de Válvulas Cardíacas , Prótesis Valvulares Cardíacas , Estenosis de la Válvula Mitral/cirugía , Infecciones Relacionadas con Prótesis/terapia , Infecciones Estafilocócicas/terapia , Infecciones Estreptocócicas/terapia , Anciano , Ampicilina/uso terapéutico , Cultivo de Sangre , Daptomicina/uso terapéutico , Desbridamiento , Ecocardiografía , Endocarditis Bacteriana/complicaciones , Endocarditis Bacteriana/microbiología , Femenino , Humanos , Embolia Intracraneal/diagnóstico por imagen , Embolia Intracraneal/etiología , Imagen por Resonancia Magnética , Resistencia a la Meticilina/fisiología , Infecciones Relacionadas con Prótesis/microbiología , Procedimientos de Cirugía Plástica , Reoperación , Staphylococcus/aislamiento & purificación , Staphylococcus/fisiología , Streptococcus anginosus/aislamiento & purificación , Streptococcus anginosus/fisiología , Sulbactam/uso terapéuticoRESUMEN
Although Streptococcus anginosus constitutes a proportion of the normal flora of the gastrointestinal and genital tracts, and the oral cavity, it has been reported that S. anginosus infection could be closely associated with abscesses at various body sites, infective endocarditis, and upper gastrointestinal cancers. The colonization in an acidic environment due to the aciduricity of S. anginosus could be the etiology of the systemic infection of the bacteria. To elucidate the aciduricity and acid tolerance mechanisms of the microbe, we examined the viability and growth of S. anginosus under acidic conditions. The viabilities of S. anginosus NCTC 10713 and Streptococcus mutans ATCC 25175 at pH 4.0 showed as being markedly higher than those of Streptococcus sanguinis ATCC 10556, Streptococcus gordonii ATCC 10558, and Streptococcus mitis ATCC 49456; however, the viability was partially inhibited by dicyclohexylcarbodiimide, an H+-ATPase inhibitor, suggesting that H+-ATPase could play a role in the viability of S. anginosus under acidic conditions. In addition, S. anginosus NCTC 10713 could grow at pH 5.0 and showed a marked arginine deiminase (ADI) activity, unlike its ΔarcA mutant, deficient in the gene encoding ADI, and other streptococcal species, which indicated that ADI could also be associated with aciduricity. These results suggest that S. anginosus has significant aciduric properties, which can be attributed to these enzyme activities.
Asunto(s)
Ácidos/metabolismo , Hidrolasas/metabolismo , ATPasas de Translocación de Protón/metabolismo , Streptococcus anginosus/efectos de los fármacos , Streptococcus anginosus/fisiología , Ácidos/farmacología , Arginina/metabolismo , Medios de Cultivo , Diciclohexilcarbodiimida/farmacología , Eliminación de Gen , Concentración de Iones de Hidrógeno , Hidrolasas/genética , Viabilidad Microbiana/efectos de los fármacos , ATPasas de Translocación de Protón/antagonistas & inhibidores , ATPasas de Translocación de Protón/genética , Streptococcus anginosus/enzimología , Streptococcus anginosus/genéticaRESUMEN
Streptococcus anginosus Group (SAG) bacteria are common causes of pyogenic infections (PIs). We examined the association between SAG species and the presence of a PI through a retrospective, observational, cohort study, between the years 2009 and 2015. All adults with clinically significant SAG infections in one hospital in Israel were assessed for association between SAG species and the presence of a PI defined as an abscess, empyema, or deep/organ space surgical site infection. Risk factors for PI were assessed using multivariate backward stepwise logistic regression analysis. We identified 263 patients with significant SAG infections, 182 (69%) of which were caused by S. anginosus, 45 (17·1%) by S treptococcus constellatus and 36 (13·7%) by S treptococcus intermedius. The mean age of the patients was 56·8 ± 19·1 years. PIs were identified among 160 (60%) of the patients and were mostly non-bacteraemic (147/160, 91·8%), while most non-PI patients had bacteraemia (70/103, 68%). S. anginosus and S. constellatus were associated with a significantly lower incidence of PI than S. intermedius, OR 0·18 (95% CI 0·06-0·53) and 0·14 (0·04-0·48), respectively. Patients with PI were younger and, in general, had less co-morbidities. S. intermedius was associated with pyogenic non-bacteraemic infections, while S. anginosus and S. constellatus were associated with bacteraemia with no abscess or empyema formation. These data may indicate differences in virulence mechanisms of these SAG bacteria.
Asunto(s)
Absceso/epidemiología , Infecciones Estreptocócicas/epidemiología , Streptococcus anginosus/fisiología , Streptococcus constellatus/fisiología , Streptococcus intermedius/fisiología , Absceso/microbiología , Adulto , Anciano , Estudios de Cohortes , Femenino , Humanos , Incidencia , Israel/epidemiología , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Especificidad de la Especie , Infecciones Estreptocócicas/microbiologíaRESUMEN
Cystic fibrosis (CF) airways harbour complex and dynamic polymicrobial communities that include many oral bacteria. Despite increased knowledge of CF airway microbiomes the interaction between established CF pathogens and other resident microbes and resulting impact on disease progression is poorly understood. Previous studies have demonstrated that oral commensal streptococci of the Anginosus group (AGS) can establish chronic pulmonary infections and become numerically dominant in CF sputa indicating that they play an important role in CF microbiome dynamics. In this study a strain of Pseudomonas aeruginosa (DWW2) of the mucoid alginate overproducing phenotype associated with chronic CF airway infection and a strain of the oral commensal AGS species Streptococcus anginosus (3a) from CF sputum were investigated for their ability to co-exist and their responses to biofilm co-culture. Bacteria in biofilms were quantified, pyocyanin expression by DWW2 was measured and the effect of AGS strain 3a on reversion of DWW2 to a non-mucoidal phenotype investigated. The virulence of DWW2, 3a and colony variant phenotypes of DWW2 in mono- and co-culture were compared in a Galleria mellonella infection model. Co-culture biofilms were formed in normoxic, hypercapnic (10% CO2) and anoxic atmospheres with the streptococcus increasing in number in co-culture, indicating that these bacteria would be able to co-exist and thrive within the heterogeneous microenvironments of the CF airway. The streptococcus caused increased pyocyanin expression by DWW2 and colony variants by stimulating reversion of the mucoid phenotype to the high pyocyanin expressing non-mucoid phenotype. The latter was highly virulent in the infection model with greater virulence when in co-culture with the streptococcus. The results of this study demonstrate that the oral commensal S. anginosus benefits from interaction with P. aeruginosa of the CF associated mucoid phenotype and modulates the behaviour of the pseudomonad in ways that may be clinically relevant.
Asunto(s)
Alginatos/metabolismo , Fibrosis Quística/microbiología , Boca/microbiología , Pseudomonas aeruginosa/metabolismo , Streptococcus anginosus/fisiología , Animales , Biopelículas , Técnicas de Cocultivo , Ácido Glucurónico/metabolismo , Ácidos Hexurónicos/metabolismo , Humanos , Larva/microbiología , Mariposas Nocturnas/crecimiento & desarrollo , VirulenciaRESUMEN
To evaluate the toxicity of smokeless tobacco products (STPs) on oral bacteria, seven smokeless tobacco aqueous extracts (STAEs) from major brands of STPs and three tobacco-specific N-nitrosamines (TSNAs) were used in a growth and viability test against 38 oral bacterial species or subspecies. All seven STAEs showed concentration-dependent effects on the growth and viability of tested oral bacteria under anaerobic culture conditions, although there were strain-to-strain variations. In the presence of 1 mg/ml STAEs, the growth of 4 strains decreased over 0.32-2.14 log10 fold, while 14 strains demonstrated enhanced growth of 0.3-1.76 log10 fold, and the growth of 21 strains was not significantly affected. In the presence of 10 mg/ml STAEs, the growth of 17 strains was inhibited 0.3-2.11 log10 fold, 18 strains showed enhanced growth of 0.3-0.97 log10 fold, and 4 strains were not significantly affected. In the presence of 50 mg/ml STAEs, the growth of 32 strains was inhibited 0.3-2.96 log10 fold, 8 strains showed enhanced growth of 0.3-1.0 log10 fold, and 2 strains were not significantly affected. All seven STAEs could promote the growth of 4 bacterial strains, including Eubacterium nodatum, Peptostreptococcus micros, Streptococcus anginosus, and Streptococcus constellatus. Exposure to STAEs modulated the viability of some bacterial strains, with 21.1-66.5% decrease for 4 strains at 1 mg/ml, 20.3-85.7% decrease for 10 strains at 10 mg/ml, 20.0-93.3% decrease for 27 strains at 50 mg/ml, and no significant effect for 11 strains at up to 50 mg/ml. STAEs from snuffs inhibited more tested bacterial strains than those from snus indicating that the snuffs may be more toxic to the oral bacteria than snus. For TSNAs, cell growth and viability of 34 tested strains were not significantly affected at up to 100 µg/ml; while the growth of P. micros was enhanced 0.31-0.54 log10 fold; the growth of Veillonella parvula was repressed 0.33-0.36 log10 fold; and the cell viabilities of 2 strains decreased 56.6-69.9%. The results demonstrate that STAEs affected the growth of some types of oral bacteria, which may affect the healthy ecological balance of oral bacteria in humans. On the other hand, TSNAs did not significantly affect the growth of the oral bacteria.
Asunto(s)
Mezclas Complejas/farmacología , Microbiota/efectos de los fármacos , Boca/microbiología , Nitrosaminas/farmacología , Tabaco sin Humo/análisis , Medios de Cultivo/química , Eubacterium/efectos de los fármacos , Eubacterium/aislamiento & purificación , Eubacterium/fisiología , Humanos , Concentración de Iones de Hidrógeno , Viabilidad Microbiana/efectos de los fármacos , Microbiota/fisiología , Peptostreptococcus/efectos de los fármacos , Peptostreptococcus/aislamiento & purificación , Peptostreptococcus/fisiología , Especificidad de la Especie , Streptococcus anginosus/efectos de los fármacos , Streptococcus anginosus/aislamiento & purificación , Streptococcus anginosus/fisiología , Streptococcus constellatus/efectos de los fármacos , Streptococcus constellatus/aislamiento & purificación , Streptococcus constellatus/fisiología , Veillonella/efectos de los fármacos , Veillonella/aislamiento & purificación , Veillonella/fisiologíaRESUMEN
Streptococcus anginosus is a commensal of mucous membranes and an emerging human pathogen. Some strains, including the type strain, display a prominent ß-hemolytic phenotype. A gene cluster (sag), encoding a variant of streptolysin S (SLS) has recently been identified as the genetic background for ß-hemolysin production in S. anginosus. In this study, we further characterized the hemolytic and cytolytic activity of the S. anginosus hemolysin in comparison with other streptococcal hemolysins. The results indicate that SLS of S. anginosus is a broad-range hemolysin able to lyse erythrocytes of different species, including horse, bovine, rabbit and even chicken. The hemolytic activity is temperature dependent, and a down-regulation of the hemolysin expression is induced in the presence of high glucose levels. Survival assays indicate that in contrast to other streptococcal species, S. anginosus does not require SLS for survival in the presence of human granulocytes. Cross-complementation studies using the sagB and sagD genes of Streptococcus pyogenes and Streptococcus dysgalactiae subsp. equisimilis demonstrated functional similarities to the S. anginosus SLS. Nevertheless, distinct differences to other streptolysin S variants were noted and provide further insights into the molecular mechanisms of SLS pathogen host interactions.
Asunto(s)
Proteínas Bacterianas/metabolismo , Eritrocitos/efectos de los fármacos , Proteínas Hemolisinas/metabolismo , Hemólisis , Streptococcus anginosus/metabolismo , Estreptolisinas/metabolismo , Animales , Bovinos , Pollos , Regulación hacia Abajo , Regulación Bacteriana de la Expresión Génica/efectos de los fármacos , Regulación Bacteriana de la Expresión Génica/efectos de la radiación , Prueba de Complementación Genética , Glucosa/metabolismo , Granulocitos/inmunología , Granulocitos/microbiología , Caballos , Humanos , Viabilidad Microbiana , Conejos , Streptococcus anginosus/inmunología , Streptococcus anginosus/fisiología , TemperaturaRESUMEN
The development of high-level daptomycin resistance (HLDR; MIC of ≥ 256 mg/liter) after exposure to daptomycin has recently been reported in viridans group streptococcus (VGS) isolates. Our study objectives were as follows: to know whether in vitro development of HLDR after exposure to daptomycin was common among clinical isolates of VGS and Streptococcus bovis; to determine whether HLDR also developed during the administration of daptomycin to treat experimental endocarditis caused by the daptomycin-susceptible, penicillin-resistant Streptococcus mitis strain S. mitis 351; and to establish whether combination with gentamicin prevented the development of HLDR in vitro and in vivo. In vitro studies were performed with 114 VGS strains (mitis group, 92; anginosus group, 10; mutans group, 8; and salivarius group, 4) and 54 Streptococcus bovis strains isolated from 168 consecutive patients with infective endocarditis diagnosed between 1995 and 2010. HLDR was only observed after 24 h of exposure to daptomycin in 27% of the mitis group, including 27% of S. mitis isolates, 47% of S. oralis isolates, and 13% of S. sanguis isolates. In our experimental model, HLDR was detected in 7/11 (63%) and 8/12 (67%) isolates recovered from vegetations after 48 h of daptomycin administered at 6 mg/kg of body weight/24 h and 10 mg/kg/24 h, respectively. In vitro, time-kill experiments showed that daptomycin plus gentamicin was bactericidal against S. mitis 351 at tested concentrations of 0.5 and 1 times the MIC and prevented the development of HLDR. In vivo, the addition of gentamicin at 1 mg/kg/8 h to both daptomycin arms prevented HLDR in 21 out of 23 (91%) rabbits. Daptomycin plus gentamicin was at least as effective as vancomycin plus gentamicin. In conclusion, HLDR develops rapidly and frequently in vitro and in vivo among mitis group streptococci. Combining daptomycin with gentamicin enhanced its activity and prevented the development of HLDR in most cases.
Asunto(s)
Antibacterianos/farmacología , Daptomicina/farmacología , Farmacorresistencia Bacteriana/efectos de los fármacos , Endocarditis Bacteriana/tratamiento farmacológico , Gentamicinas/farmacología , Infecciones Estreptocócicas/tratamiento farmacológico , Streptococcus mitis/efectos de los fármacos , Animales , Sinergismo Farmacológico , Quimioterapia Combinada , Endocarditis Bacteriana/complicaciones , Endocarditis Bacteriana/microbiología , Humanos , Pruebas de Sensibilidad Microbiana , Conejos , Especificidad de la Especie , Infecciones Estreptocócicas/complicaciones , Infecciones Estreptocócicas/microbiología , Streptococcus anginosus/efectos de los fármacos , Streptococcus anginosus/fisiología , Streptococcus bovis/efectos de los fármacos , Streptococcus bovis/fisiología , Streptococcus mitis/fisiología , Streptococcus mutans/efectos de los fármacos , Streptococcus mutans/fisiología , Vancomicina/farmacologíaRESUMEN
INTRODUCTION: Streptococcus anginosus group (SAG) bacteria are opportunistic pathogens and a major cause of pulpal infection and subsequent abscess formation. Understanding of the processes involved in SAG oral infections has been limited by the lack of an appropriate model system. METHODS: Cocultures of SAG bacteria and mammalian tooth slices were maintained using a combination of Dulbecco modified eagle medium and brain-heart infusion broth at 60 rpm, 37°C, 5% CO(2) for 4, 8, or 24 hours before histologic examination or staining with acridine orange/ethidium bromide. Tooth slices were also incubated as described with SAG bacteria stained with fluorescein diacetate. Pulps were extirpated from infected and sterile cultured tooth slices, messenger RNA was extracted and converted to complementary DNA, and polymerase chain reaction were performed for genes encoding tumor necrosis factor α, interleukin 1ß, and interleukin-6. RESULTS: SAG bacteria were able to adhere directly to the central region of the pulpal matrix in small foci that were associated with a localized matrix breakdown. Acridine orange-ethidium bromide staining and cell counts indicated a decrease in mammalian cell viability with increasing incubation times in the presence of SAG bacteria. The increased expression of tumor necrosis factor α and interleukin 1ß was detected in infected tooth slices. CONCLUSIONS: A novel ex vivo model system has been developed that allows coculture of SAG bacteria with a 3-dimensional organotypic tooth slice. The model allows observation of bacterial growth patterns and subsequent responses from host tissues. Therefore, it may be of future use in testing the efficacy of both antimicrobial and anti-inflammatory treatments for use in endodontic therapy.
Asunto(s)
Enfermedades de la Pulpa Dental/microbiología , Pulpa Dental/microbiología , Infecciones Estreptocócicas/microbiología , Streptococcus anginosus/fisiología , Streptococcus constellatus/fisiología , Naranja de Acridina , Animales , Adhesión Bacteriana/fisiología , Carga Bacteriana , Técnicas Bacteriológicas , Muerte Celular/fisiología , Supervivencia Celular/fisiología , Técnicas de Cocultivo , Medios de Cultivo , Pulpa Dental/patología , Enfermedades de la Pulpa Dental/patología , Dentina/microbiología , Dentina/patología , Etidio , Fibroblastos/patología , Fluoresceínas , Colorantes Fluorescentes , Incisivo/microbiología , Incisivo/patología , Interleucina-1beta/análisis , Interleucina-6/análisis , Masculino , Odontoblastos/patología , Técnicas de Cultivo de Órganos , Ratas , Ratas Wistar , Streptococcus anginosus/crecimiento & desarrollo , Streptococcus constellatus/crecimiento & desarrollo , Factores de Tiempo , Factor de Necrosis Tumoral alfa/análisisRESUMEN
Members of the Streptococcus anginosus group (SAGs) are significant pathogens. However, their pathogenic mechanisms are incompletely understood. This study investigates the adherence of SAGs to the matrix proteoglycans decorin and biglycan of soft gingival and alveolar bone. Recombinant chondroitin 4-sulphate(C4S)-conjugated decorin and biglycan were synthesised using mammalian expression systems. C4S-conjugated decorin/biglycan and dermatan sulphate (DS) decorin/biglycan were isolated from ovine alveolar bone and gingival connective tissue, respectively. Using surface plasmon resonance, adherence of the SAGs S. anginosus, Streptococcus constellatus and Streptococcus intermedius to immobilised proteoglycan was assessed as a function of real-time biofilm formation. All isolates adhered to gingival proteoglycan, 59% percent of isolates adhered to alveolar proteoglycans, 70% to recombinant decorin and 76% to recombinant biglycan. Higher adherence was generally noted for S. constellatus and S. intermedius isolates. No differences in adherence were noted between commensal and pathogenic strains to decorin or biglycan. DS demonstrated greater adherence compared to C4S. Removal of the glycosaminoglycan chains with chondroitinase ABC resulted in no or minimal adherence for all isolates. These results suggest that SAGs bind to the extracellular matrix proteoglycans decorin and biglycan, with interaction mediated by the conjugated glycosaminoglycan chain.
Asunto(s)
Adhesión Bacteriana , Biglicano/metabolismo , Decorina/metabolismo , Matriz Extracelular/microbiología , Streptococcus anginosus/fisiología , Streptococcus constellatus/fisiología , Streptococcus intermedius/fisiología , Animales , Biglicano/genética , Biglicano/aislamiento & purificación , Biopelículas/crecimiento & desarrollo , Decorina/genética , Decorina/aislamiento & purificación , Encía/química , Mandíbula/química , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Ovinos , Resonancia por Plasmón de SuperficieRESUMEN
BACKGROUND: The co-aggregation of oral bacteria leads to their clearance from the oral cavity. Poor oral hygiene and high saliva viscosity are common amongst the elderly; thus, they frequently suffer from pneumonia caused by the aspiration of oral microorganisms. OBJECTIVES: To examine the direct effect of saliva viscosity on the co-aggregation of oral streptococci with actinomyces. MATERIALS AND METHODS: Fifteen oral streptococcal and a single actinomyces strain were used. Co-aggregation was assessed by a visual assay in phosphate buffer and a spectrophotometric assay in the same buffer containing 0-60% glycerol or whole saliva. RESULTS: Nine oral streptococci co-aggregated with Actinomyces naeslundii ATCC12104 in the visual assay and were subsequently used for the spectrophotometric analysis. All tested strains displayed a decrease in co-aggregation with increasing amounts of glycerol in the buffer. The co-aggregation of Streptococcus oralis with A. naeslundii recovered to baseline level following the removal of glycerol. The per cent co-aggregation of S. oralis with A. naeslundii was significantly correlated with the viscosity in unstimulated and stimulated whole saliva samples (correlation coefficients: -0.52 and -0.48, respectively). CONCLUSION: This study suggests that saliva viscosity affects the co-aggregation of oral streptococci with actinomyces and that bacterial co-aggregation decreases with increasing saliva viscosity.
Asunto(s)
Actinomyces/fisiología , Saliva/fisiología , Streptococcus/fisiología , Actinomyces/efectos de los fármacos , Adulto , Tampones (Química) , Glicerol/administración & dosificación , Glicerol/farmacología , Humanos , Interacciones Microbianas/efectos de los fármacos , Interacciones Microbianas/fisiología , Persona de Mediana Edad , Fosfatos/química , Saliva/microbiología , Espectrofotometría , Streptococcus/efectos de los fármacos , Streptococcus anginosus/efectos de los fármacos , Streptococcus anginosus/fisiología , Streptococcus constellatus/efectos de los fármacos , Streptococcus constellatus/fisiología , Streptococcus gordonii/efectos de los fármacos , Streptococcus gordonii/fisiología , Streptococcus intermedius/efectos de los fármacos , Streptococcus intermedius/fisiología , Streptococcus mitis/efectos de los fármacos , Streptococcus mitis/fisiología , Streptococcus mutans/efectos de los fármacos , Streptococcus mutans/fisiología , Streptococcus oralis/efectos de los fármacos , Streptococcus oralis/fisiología , Streptococcus pneumoniae/efectos de los fármacos , Streptococcus pneumoniae/fisiología , Streptococcus sanguis/efectos de los fármacos , Streptococcus sanguis/fisiología , Viscosidad , Adulto JovenRESUMEN
Oral viridans group streptococci are the major commensal bacteria of the supragingival oral biofilm and have been detected in human atheromatous plaque. Atherosclerosis involves an ongoing inflammatory response, reportedly involving chronic infection caused by multiple pathogens. The aim of this study was to examine the invasion of human aortic endothelial cells (HAECs) by oral viridans group streptococci and the subsequent cytokine production by viable invaded HAECs. The invasion of HAECs by bacteria was examined using antibiotic protection assays and was visualized by confocal scanning laser microscopy. The inhibitory effects of catalase and cytochalasin D on the invasion of HAECs were also examined. The production of cytokines by invaded or infected HAECs was determined using enzyme-linked immunosorbent assays, and a real-time polymerase chain reaction method was used to evaluate the expression of cytokine messenger RNA. The oral streptococci tested were capable of invading HAECs. The number of invasive bacteria increased with the length of the co-culture period. After a certain co-culture period, some organisms were cytotoxic to the HAECs. Catalase and cytochalasin D inhibited the invasion of HAECs by the organism. HAECs invaded by Streptococcus mutans Xc, Streptococcus gordonii DL1 (Challis), Streptococcus gordonii ATCC 10558 and Streptococcus salivarius ATCC 13419 produced more cytokine(s) (interleukin-6, interleukin-8, monocyte chemoattractant protein-1) than non-invaded HAECs. The HAECs invaded by S. mutans Xc produced the largest amounts of cytokines, and the messenger RNA expression of cytokines by invaded HAECs increased markedly compared with that by non-invaded HAECs. These results suggest that oral streptococci may participate in the pathogenesis of atherosclerosis.
Asunto(s)
Aorta/microbiología , Citocinas/biosíntesis , Células Endoteliales/microbiología , Endotelio Vascular/microbiología , Mediadores de Inflamación/metabolismo , Boca/microbiología , Estreptococos Viridans/fisiología , Aorta/citología , Aterosclerosis/microbiología , Catalasa/farmacología , Células Cultivadas , Quimiocina CCL2/biosíntesis , Técnicas de Cocultivo , Citocalasina D/farmacología , Células Endoteliales/inmunología , Endotelio Vascular/citología , Humanos , Interleucina-6/biosíntesis , Interleucina-8/biosíntesis , Microscopía Confocal , Streptococcus/fisiología , Streptococcus anginosus/fisiología , Streptococcus gordonii/fisiología , Streptococcus intermedius/fisiología , Streptococcus mitis/fisiología , Streptococcus mutans/fisiología , Streptococcus oralis/fisiología , Estreptococos Viridans/efectos de los fármacos , Estreptococos Viridans/inmunología , VirulenciaRESUMEN
The terminology and classification of the Anginosus group streptococci has been inconsistent. We tested the utility of 16S rRNA gene and tuf gene sequencing and conventional biochemical tests for the reliable differentiation of the Anginosus group streptococci. Biochemical testing included Rapid ID 32 Strep, API Strep, Fluo-Card Milleri, Wee-tabs, and Lancefield antigen typing. Altogether, 61 Anginosus group isolates from skin and soft tissue infections and four reference strains were included. Our results showed a good agreement between 16S rRNA gene and tuf gene sequencing. Using the full sequence was less discriminatory than using the first part of the 16S rRNA gene. The three species could not be separated with the API 20 Strep test. Streptococcus intermedius could be differentiated from the other two species by beta-galactosidase (ONPG) and beta-N-acetyl-glucosaminidase reactions. Rapid ID 32 Strep beta-glucosidase reaction was useful in separating S. anginosus strains from S. constellatus. In conclusion, both 16S rRNA gene and tuf gene sequencing can be used for the reliable identification of the Anginosus group streptococci. S. intermedius can be readily differentiated from the other two species by phenotypic tests; however, 16S rRNA gene or tuf gene sequencing may be needed for separating some strains of S. constellatus from S. anginosus.
Asunto(s)
Técnicas Bacteriológicas/métodos , Streptococcus anginosus/clasificación , Streptococcus constellatus/clasificación , Streptococcus intermedius/clasificación , Técnicas de Tipificación Bacteriana/métodos , ADN Bacteriano/química , ADN Bacteriano/genética , ADN Ribosómico/química , ADN Ribosómico/genética , Humanos , Factor Tu de Elongación Peptídica/genética , ARN Ribosómico 16S/genética , Análisis de Secuencia de ADN , Enfermedades Cutáneas Bacterianas/microbiología , Infecciones de los Tejidos Blandos/microbiología , Infecciones Estreptocócicas/microbiología , Streptococcus anginosus/genética , Streptococcus anginosus/aislamiento & purificación , Streptococcus anginosus/fisiología , Streptococcus constellatus/genética , Streptococcus constellatus/aislamiento & purificación , Streptococcus constellatus/fisiología , Streptococcus intermedius/genética , Streptococcus intermedius/aislamiento & purificación , Streptococcus intermedius/fisiologíaRESUMEN
The ability of oral bacteria to enter a non-growing state is believed to be an important mechanism for survival in the starved micro-environments of the oral cavity. In this study, we examined the reactivation of nutrient-deprived cells of two oral bacteria in biofilms, Streptococcus anginosus and Lactobacillus salivarius. Non-growing cells were generated by incubation in 10 mM potassium phosphate buffer for 24 h and the results were compared to those of planktonic cultures. When both types of cells were shifted from a rich, peptone-yeast extract-glucose (PYG) medium to buffer for 24 h, dehydrogenase and esterase activity measured by the fluorescent dyes 5-cyano-2,3-ditolyl-tetrazolium chloride (CTC) and fluorescein diacetate (FDA), respectively, was absent in both species. However, the membranes of the vast majority of nutrient-deprived cells remained intact as assessed by LIVE/DEAD staining. Metabolic reactivation of the nutrient-deprived biofilm cells was not observed for at least 48 h following addition of fresh PYG medium, whereas the non-growing planktonic cultures of the same two strains were in rapid growth in less than 2 h. At 72 h, the S. anginosus biofilm cells had recovered 78 % of the dehydrogenase activity and 61 % of the esterase activity and the biomass mm(-2) had increased by 30-35 %. With L. salivarius at 72 h, the biofilms had recovered 56 % and 75 % of dehydrogenase and esterase activity, respectively. Reactivation of both species in biofilms was enhanced by removal of glucose from PYG, and S. anginosus cells were particularly responsive to yeast extract (YE) medium. The data suggest that the low reactivity of non-growing biofilm cells to the introduction of fresh nutrients may be a survival strategy employed by micro-organisms in the oral cavity.
Asunto(s)
Biopelículas/crecimiento & desarrollo , Medios de Cultivo/metabolismo , Cavidad Pulpar/microbiología , Lactobacillus/fisiología , Infecciones Estreptocócicas/microbiología , Streptococcus anginosus/fisiología , Biomasa , Medios de Cultivo/química , Placa Dental/microbiología , Humanos , Lactobacillus/crecimiento & desarrollo , Lactobacillus/aislamiento & purificación , Streptococcus anginosus/crecimiento & desarrollo , Streptococcus anginosus/aislamiento & purificaciónRESUMEN
INTRODUCTION: Autoinducer-2 (AI-2) is a widespread communication-signal molecule that allows bacteria to sense and react to environmental factors. In some streptococci AI-2 is reported to be involved in virulence expression and biofilm formation. It has earlier been shown that the alga Delisea pulchra produces bromated furanones, which prevent bacterial colonization of the algae. METHODS AND RESULTS: We have previously published a novel and simple synthesis of (Z)-5-bromomethylene-2(5H)-furanone. In this study we showed that our synthesized furanone inhibited biofilm formation and bioluminescence induction by Streptococcus anginosus, Streptococcus intermedius, and Streptococcus mutans, as well as bioluminescence induction by Vibrio harveyi BB152. CONCLUSION: We suggest that the effect is linked to interference with the AI-2 signaling pathway because adding furanone to the medium had no effect on the ability of the AI-2-defective S. anginosus luxS and S. intermedius luxS mutants to form biofilms.
Asunto(s)
4-Butirolactona/análogos & derivados , Biopelículas/efectos de los fármacos , Furanos/farmacología , Homoserina/análogos & derivados , Lactonas/antagonistas & inhibidores , Transducción de Señal/efectos de los fármacos , Streptococcus/fisiología , 4-Butirolactona/farmacología , Homoserina/antagonistas & inhibidores , Humanos , Luminiscencia , Boca/microbiología , Streptococcus/efectos de los fármacos , Streptococcus anginosus/efectos de los fármacos , Streptococcus anginosus/fisiología , Streptococcus intermedius/efectos de los fármacos , Streptococcus intermedius/fisiología , Streptococcus mutans/efectos de los fármacos , Streptococcus mutans/fisiología , Vibrio/efectos de los fármacosRESUMEN
Interactions between Enterococcus faecalis and other species found in root canal infections might be important for the development and persistence of periapical disease. The aim of this study was to investigate the coaggregation interactions between E. faecalis clinical isolates and species previously shown to survive and induce apical periodontitis in monkeys: Peptostreptococcus anaerobius, Prevotella oralis, Fusobacterium nucleatum, and Streptococcus anginosus. Intergeneric coaggregation assays were conducted in duplicate with observations scored immediately at 0 h, 1 h and 24 h after mixing of combinations of strains. All E. faecalis strains (n = 53) coaggregated with F. nucleatum; E. faecalis did not coaggregate with P. anaerobius or S. anginosus. One strain, E. faecalis E1, coaggregated with P. oralis, with aggregates visible at 1 h. Coaggregation interactions between E. faecalis and F. nucleatum observed in this study suggest a potential role for this combination in endodontic infections.
Asunto(s)
Adhesión Bacteriana/fisiología , Cavidad Pulpar/microbiología , Enterococcus faecalis/fisiología , Boca/microbiología , Periodontitis Periapical/microbiología , Animales , Técnicas Bacteriológicas , Enterococcus faecalis/clasificación , Fusobacterium nucleatum/fisiología , Haplorrinos , Peptostreptococcus/fisiología , Prevotella/fisiología , Streptococcus anginosus/fisiología , Factores de TiempoRESUMEN
The purpose of this study was twofold: first, to determine the influence on the healing of the periapical tissues when selected bacterial strains and combinations thereof remain after root canal treatment; and, second, the relationship to healing of the quality of the root filling. In eight monkeys, 175 root canals, previously infected with combinations of four or five bacterial strains and with radiographically verified apical periodontitis, were endodontically treated, bacteriologically controlled, and permanently obturated. After 2-2.5 yr, the periapical regions were radiographically and histologically examined. Of these teeth, 48 root canals were also examined for bacteria remaining after removal of the root fillings. When bacteria remained after the endodontic treatment, 79% of the root canals showed non-healed periapical lesions, compared with 28% where no bacteria were found. Combinations of residual bacterial species were more frequently related to non-healed lesions than were single strains. When no bacteria remained, healing occurred independently of the quality of the root filling. In contrast, when bacteria remained, there was a greater correlation with non-healing in poor-quality root fillings than in technically well-performed fillings. In root canals where bacteria were found after removal of the root filling, 97% had not healed, compared with 18% for those root canals with no bacteria detected. The present study demonstrates the importance of obtaining a bacteria-free root canal system before permanent root filling in order to achieve optimal healing conditions for the periapical tissues.
Asunto(s)
Fenómenos Fisiológicos Bacterianos , Periodontitis Periapical/terapia , Tejido Periapical/fisiopatología , Obturación del Conducto Radicular , Tratamiento del Conducto Radicular/métodos , Animales , Infecciones por Bacteroidaceae/fisiopatología , Cavidad Pulpar/microbiología , Enterococcus faecalis/fisiología , Femenino , Infecciones por Fusobacterium/fisiopatología , Fusobacterium nucleatum/fisiología , Infecciones por Bacterias Grampositivas/fisiopatología , Macaca fascicularis , Peptostreptococcus/fisiología , Periodontitis Periapical/microbiología , Periodontitis Periapical/fisiopatología , Tejido Periapical/microbiología , Prevotella/fisiología , Materiales de Obturación del Conducto Radicular/uso terapéutico , Irrigantes del Conducto Radicular/uso terapéutico , Preparación del Conducto Radicular/instrumentación , Infecciones Estreptocócicas/fisiopatología , Streptococcus anginosus/fisiología , Factores de Tiempo , Cicatrización de Heridas/fisiologíaRESUMEN
The autoinducer-2 signal (AI-2) produced by several Gram-positive and Gram-negative bacteria mediates interspecies communication. In this study we were able to identify an orthologue of luxS, required for the synthesis of AI-2 signals, in Streptococcus anginosus. Comparative analyses revealed conserved sequences in the predicted S. anginosus LuxS. Expression of luxS was highest during early exponential growth phase. Compared to other oral streptococci, conditioned media from growth of members of the anginosus group were the most efficient in inducing bioluminescence in Vibrio harveyi, indicative of AI-2 signalling. Disruption of luxS in S. anginosus resulted in a mutant deficient in biofilm formation, whereas no effect on planktonic growth rate was observed under various growth conditions. S. anginosus is part of the human flora found in biofilms of the oral cavity, as well as of the upper respiratory, gastrointestinal and urogenital tracts. Such habitats harbour large varieties of bacterial species, among which cell-cell communication may play an important role. S. anginosus has also been associated with purulent infections and cancer in the upper digestive tract. Knowledge about the molecular mechanisms involved in S. anginosus communication is important for understanding its commensalism and its pathogenic transition.
Asunto(s)
Proteínas Bacterianas/fisiología , Biopelículas/crecimiento & desarrollo , Liasas de Carbono-Azufre/fisiología , Transducción de Señal , Streptococcus anginosus/fisiología , Adaptación Fisiológica , Proteínas Bacterianas/genética , Liasas de Carbono-Azufre/genética , Medios de Cultivo Condicionados , Regulación Bacteriana de la Expresión Génica , Luciferasas de la Bacteria/metabolismo , Luminiscencia , Microscopía Electrónica de Rastreo , Mutagénesis Insercional , Transducción de Señal/genética , Streptococcus anginosus/genética , Vibrio/efectos de los fármacosRESUMEN
Viridans streptococci, including Streptococcus anginosus, are a common cause of infective endocarditis in humans. Adherence mechanisms involved in colonization of non-diseased native valves (present in 40% of native valve endocarditis) are unknown. We have previously shown that an endocarditis isolate of S. anginosus adheres to exposed basement membrane of human and porcine valve tissue in a laminin dependent manner. We now describe the partial purification of an 80 kDa putative laminin binding protein (PLBP) by biochemical methods. Amino acid sequence of PLBP peptides is similar to substrate binding proteins of ABC transporters in other Gram-positive cocci.