RESUMEN
To elucidate the host genetic loci affecting severity of SARS-CoV-2 infection, or Coronavirus disease 2019 (COVID-19), is an emerging issue in the face of the current devastating pandemic. Here, we report a genome-wide association study (GWAS) of COVID-19 in a Japanese population led by the Japan COVID-19 Task Force, as one of the initial discovery GWAS studies performed on a non-European population. Enrolling a total of 2,393 cases and 3,289 controls, we not only replicated previously reported COVID-19 risk variants (e.g., LZTFL1, FOXP4, ABO, and IFNAR2), but also found a variant on 5q35 (rs60200309-A at DOCK2) that was associated with severe COVID-19 in younger (<65 years of age) patients with a genome-wide significant p-value of 1.2 x 10-8 (odds ratio = 2.01, 95% confidence interval = 1.58-2.55). This risk allele was prevalent in East Asians, including Japanese (minor allele frequency [MAF] = 0.097), but rarely found in Europeans. Cross-population Mendelian randomization analysis made a causal inference of a number of complex human traits on COVID-19. In particular, obesity had a significant impact on severe COVID-19. The presence of the population-specific risk allele underscores the need of non-European studies of COVID-19 host genetics.
RESUMEN
The aim of this in vitro study was to determine the maximum inhibitory dilution (MID) of four cetylpyridinium chloride (CPC)-based mouthwashes: CPC+Propolis, CPC+Malva, CPC+Eucaliptol+Juá+Romã+Propolis (Natural Honey) and CPC (Cepacol), against 28 Staphylococcus aureus field strains, using the agar dilution method. Decimal dilutions ranging from 1/10 to 1/655,360 were prepared and added to Mueller Hinton Agar. Strains were inoculated using Steers multipoint inoculator. The inocula were seeded onto the surface of the culture medium in Petri dishes containing different dilutions of the mouthwashes. The dishes were incubated at 37 degrees C for 24 h. For readings, the MID was considered as the maximum dilution of mouthwash still capable of inhibiting microbial growth. The obtained data showed that CPC+Propolis had antimicrobial activity against 27 strains at 1/320 dilution and against all 28 strains at 1/160 dilution, CPC+Malva inhibited the growth of all 28 strains at 1/320 dilution, CPC+Eucaliptol+Juá+Romã+Propolis inhibited the growth of 2 strains at 1/640 dilution and all 28 strains at 1/320 dilution, and Cepacol showed antimicrobial activity against 3 strains at 1/320 dilution and against all 28 strains at 1/160 dilution. Data were submitted to Kruskal-Wallis test, showing that the MID of Cepacol was lower than that determined for the other products (p<0.05). In conclusion, CPC-mouthwashes showed antimicrobial activity against S. aureus and the addition of other substances to CPC improved its antimicrobial effect.
Asunto(s)
Antiinfecciosos Locales/farmacología , Cetilpiridinio/farmacología , Antisépticos Bucales/farmacología , Staphylococcus aureus/efectos de los fármacos , Antiinfecciosos Locales/administración & dosificación , Cetilpiridinio/administración & dosificación , Ciclohexanoles/administración & dosificación , Relación Dosis-Respuesta a Droga , Combinación de Medicamentos , Eucaliptol , Malva , Pruebas de Sensibilidad Microbiana , Monoterpenos/administración & dosificación , Antisépticos Bucales/administración & dosificación , Aceites de Plantas/administración & dosificación , Própolis/administración & dosificaciónRESUMEN
The aim of this in vitro study was to determine the maximum inhibitory dilution (MID) of four cetylpyridinium chloride (CPC)-based mouthwashes: CPC+Propolis, CPC+Malva, CPC+Eucaliptol+Juá+Romã+Propolis (Natural Honey®) and CPC (Cepacol®), against 28 Staphylococcus aureus field strains, using the agar dilution method. Decimal dilutions ranging from 1/10 to 1/655,360 were prepared and added to Mueller Hinton Agar. Strains were inoculated using Steers multipoint inoculator. The inocula were seeded onto the surface of the culture medium in Petri dishes containing different dilutions of the mouthwashes. The dishes were incubated at 37ºC for 24 h. For readings, the MID was considered as the maximum dilution of mouthwash still capable of inhibiting microbial growth. The obtained data showed that CPC+Propolis had antimicrobial activity against 27 strains at 1/320 dilution and against all 28 strains at 1/160 dilution, CPC+Malva inhibited the growth of all 28 strains at 1/320 dilution, CPC+Eucaliptol+Juá+Romã+Propolis inhibited the growth of 2 strains at 1/640 dilution and all 28 strains at 1/320 dilution, and Cepacol® showed antimicrobial activity against 3 strains at 1/320 dilution and against all 28 strains at 1/160 dilution. Data were submitted to Kruskal-Wallis test, showing that the MID of Cepacol® was lower than that determined for the other products (p<0.05). In conclusion, CPC-mouthwashes showed antimicrobial activity against S. aureus and the addition of other substances to CPC improved its antimicrobial effect.
Asunto(s)
Antiinfecciosos Locales/farmacología , Cetilpiridinio/farmacología , Antisépticos Bucales/farmacología , Staphylococcus aureus/efectos de los fármacos , Antiinfecciosos Locales/administración & dosificación , Cetilpiridinio/administración & dosificación , Ciclohexanoles/administración & dosificación , Relación Dosis-Respuesta a Droga , Combinación de Medicamentos , Malva , Pruebas de Sensibilidad Microbiana , Monoterpenos/administración & dosificación , Antisépticos Bucales/administración & dosificación , Aceites de Plantas/administración & dosificación , Própolis/administración & dosificaciónRESUMEN
Molecular methods that permit the simultaneous detection and quantification of a large number of microbial species are currently employed in the evaluation of complex ecosystems. The checkerboard DNA-DNA hybridization technique enables the simultaneous identification of distinct bacterial species in a large number of dental samples. The original technique employed digoxigenin-labeled whole genomic DNA probes which were detected by chemiluminescence. In this study, we present an alternative protocol for labeling and detecting whole genomic DNA probes in the Checkerboard DNA-DNA hybridization method. Whole genomic DNA was extracted from five bacterial species and labeled with fluorescein. The fluorescein labeled whole genomic DNA probes were hybridized against whole genomic DNA or subgingival plaque samples in a checkerboard hybridization format, followed by chemiluminescent detection. Our results reveal that fluorescein is a viable and adequate alternative labeling reagent to be employed in the checkerboard DNA-DNA hybridization technique.
Asunto(s)
Fluoresceína , Hibridación de Ácido Nucleico/métodos , Coloración y Etiquetado/métodos , Sondas de ADN/química , Genoma Bacteriano/genética , LuminiscenciaRESUMEN
A recent innovation in medical field is the use of DNA probes in microbiological diagnosis of the oral cavity. Thus, this study has the objective to present the mainly characteristics of Checkerboard DNA-DNA Hybridization method for bacterial pathogens identification related to periimplantitis, commonly disease found in the oral cavity, as wells as, to show the uses and applications of this technique.
Una innovación reciente en medicina es la utilización de sondas de DNA para diagnóstico microbiológico. Este trabajo tiene como objetivo, presentar las principales características del método Checkerboard DNA-DNA Hybridization para la identificación de bacterias patógenas associadas a periimplantite en la cavidad oral, mostrando las diferentes utilizaciones y aplicaciones de esta técnica.