ABSTRACT
We present results from an analysis of all data taken by the BICEP2, Keck Array, and BICEP3 CMB polarization experiments up to and including the 2018 observing season. We add additional Keck Array observations at 220 GHz and BICEP3 observations at 95 GHz to the previous 95/150/220 GHz dataset. The Q/U maps now reach depths of 2.8, 2.8, and 8.8 µK_{CMB} arcmin at 95, 150, and 220 GHz, respectively, over an effective area of ≈600 square degrees at 95 GHz and ≈400 square degrees at 150 and 220 GHz. The 220 GHz maps now achieve a signal-to-noise ratio on polarized dust emission exceeding that of Planck at 353 GHz. We take auto- and cross-spectra between these maps and publicly available WMAP and Planck maps at frequencies from 23 to 353 GHz and evaluate the joint likelihood of the spectra versus a multicomponent model of lensed ΛCDM+r+dust+synchrotron+noise. The foreground model has seven parameters, and no longer requires a prior on the frequency spectral index of the dust emission taken from measurements on other regions of the sky. This model is an adequate description of the data at the current noise levels. The likelihood analysis yields the constraint r_{0.05}<0.036 at 95% confidence. Running maximum likelihood search on simulations we obtain unbiased results and find that σ(r)=0.009. These are the strongest constraints to date on primordial gravitational waves.
ABSTRACT
We present results from an analysis of all data taken by the bicep2/Keck CMB polarization experiments up to and including the 2015 observing season. This includes the first Keck Array observations at 220 GHz and additional observations at 95 and 150 GHz. The Q and U maps reach depths of 5.2, 2.9, and 26 µK_{CMB} arcmin at 95, 150, and 220 GHz, respectively, over an effective area of ≈400 square degrees. The 220 GHz maps achieve a signal to noise on polarized dust emission approximately equal to that of Planck at 353 GHz. We take auto and cross spectra between these maps and publicly available WMAP and Planck maps at frequencies from 23 to 353 GHz. We evaluate the joint likelihood of the spectra versus a multicomponent model of lensed-ΛCDM+r+dust+synchrotron+noise. The foreground model has seven parameters, and we impose priors on some of these using external information from Planck and WMAP derived from larger regions of sky. The model is shown to be an adequate description of the data at the current noise levels. The likelihood analysis yields the constraint r_{0.05}<0.07 at 95% confidence, which tightens to r_{0.05}<0.06 in conjunction with Planck temperature measurements and other data. The lensing signal is detected at 8.8σ significance. Running a maximum likelihood search on simulations we obtain unbiased results and find that σ(r)=0.020. These are the strongest constraints to date on primordial gravitational waves.
ABSTRACT
The present studies demonstrate that antisera directed against Streptococcus pneumoniae type 14 is opsonic for group B streptococci type III in a neutrophile-mediated bactericidal assay. Specificity was demonstrated by the observations that group B streptococci type III and S. pneumoniae type 14 adsorbed the opsonic activity of anti-S. pneumoniae type 14 antisera. Group B streptococci strain 090R (devoid of type antigens) and S. pneumoniae type 3, did not remove the opsonic activity of anti-S. pneumoniae type 14 serum. In vivo studies using a suckling rat model of neonatal group B streptococcal type III sepsis demonstrated that antisera directed against S. pneumoniae type 14 was highly protective.
Subject(s)
Antibodies, Bacterial , Streptococcal Infections/therapy , Streptococcus agalactiae/immunology , Streptococcus pneumoniae/immunology , Animals , Antibody Specificity , Blood Bactericidal Activity , Cross Reactions , Disease Models, Animal , Immunotherapy , Neutrophils/immunology , Opsonin Proteins , Polysaccharides, Bacterial/immunology , RatsABSTRACT
Amniotic fluid specimens from 110 patients in labor were examined for neutrophils and bacteria. Patients with neutrophils in their amniotic fluid had significantly higher fever indices than patients with clear amniotic fluid. The highest fever indices were found in those patients who delivered by cesarean section after neutrophils were present in their amniotic fluid. Febrile morbidity was significantly reduced in a group of 24 such patients by giving prophylactic antibiotics.
Subject(s)
Amniotic Fluid/cytology , Bacteria , Labor, Obstetric , Neutrophils , Pregnancy Complications, Infectious/diagnosis , Adult , Amniotic Fluid/microbiology , Ampicillin/therapeutic use , Bacteria/isolation & purification , Bacterial Infections/drug therapy , Bacterial Infections/pathology , Cesarean Section , Delivery, Obstetric , Female , Fever/microbiology , Humans , Pregnancy , Pregnancy Complications, Infectious/drug therapyABSTRACT
Antisera were raised against intact crotoxin (Crotalus durissus terrificus), Mojave toxin (Crotalus scutulatus scutulatus) and concolor toxin (Crotalus viridis concolor), as well as the subunits of crotoxin. Double immunodiffusion and enzyme-linked immunosorbent assays (ELISA) demonstrated antigenic similarity between these three purified toxins and their subunits. Additionally, when crotoxin antisera were pre-incubated with each of the three toxins before injection, the lethal activity of all were neutralized equally well. Antiserum was considerably more effective in neutralizing crotoxin in vivo when the toxin was injected i.m. than when injected i.v. Antisera against both intact crotoxin and its basic subunit were an order of magnitude more effective than crotoxin acidic subunit antiserum in crotoxin neutralization. Purified phospholipase A2 from Crotalus adamanteus and Crotalus atrox showed weak cross-reactivity with antisera raised against intact crotoxin and its subunits in the ELISA. Our results suggest that crotalid neurotoxins can be detected and neutralized by polyclonal antibodies raised against any intact toxin or basic subunit in this group of homologous toxins.
Subject(s)
Crotalid Venoms/immunology , Crotoxin/immunology , Immune Sera/immunology , Animals , Cross Reactions , Crotoxin/toxicity , Enzyme-Linked Immunosorbent Assay , Immunodiffusion , Male , Mice , Mice, Inbred ICR , Neurotoxins/immunology , Neutralization Tests , RabbitsSubject(s)
Dog Diseases/etiology , Glossitis/veterinary , Acinetobacter/isolation & purification , Animals , Bacillus/isolation & purification , Biopsy , Dog Diseases/chemically induced , Dog Diseases/pathology , Dogs , Enterococcus faecalis/isolation & purification , Environment, Controlled , Escherichia coli/isolation & purification , Glossitis/chemically induced , Glossitis/etiology , Glossitis/pathology , Humidity , Iodine , Physical Exertion , Sunlight , Temperature , Tetracycline/adverse effects , Time Factors , Tongue/microbiology , Tongue/pathology , VietnamSubject(s)
Anti-Bacterial Agents/administration & dosage , Brucellosis/veterinary , Dog Diseases/drug therapy , Ampicillin/administration & dosage , Ampicillin/therapeutic use , Animals , Anti-Bacterial Agents/therapeutic use , Autopsy , Biopsy , Blood/microbiology , Bone Marrow/microbiology , Brucella/isolation & purification , Brucellosis/drug therapy , Brucellosis/immunology , Brucellosis/microbiology , Dogs , Female , Lymph Nodes/microbiology , Male , Streptomycin/administration & dosage , Streptomycin/therapeutic use , Tetracycline/administration & dosage , Tetracycline/therapeutic useSubject(s)
Cat Diseases , Mycetoma/veterinary , Streptomyces , Animals , Cat Diseases/etiology , Cat Diseases/pathology , Cat Diseases/surgery , Cats , Male , Mycetoma/etiology , Mycetoma/pathology , Mycetoma/surgerySubject(s)
Abscess/veterinary , Dog Diseases/etiology , Pseudomonas Infections/veterinary , Pseudomonas/isolation & purification , Abscess/etiology , Abscess/microbiology , Abscess/pathology , Abscess/surgery , Animals , Dogs , Male , Pseudomonas/pathogenicity , Pseudomonas Infections/etiology , Skin Diseases, Infectious/etiology , Skin Diseases, Infectious/veterinarySubject(s)
Ampicillin/therapeutic use , Brucellosis/veterinary , Dog Diseases/drug therapy , Tetracycline/therapeutic use , Administration, Oral , Ampicillin/administration & dosage , Animals , Antigens, Bacterial , Blood/microbiology , Bone Marrow/microbiology , Brucella/immunology , Brucella/isolation & purification , Brucellosis/drug therapy , Brucellosis/immunology , Brucellosis/microbiology , Dog Diseases/immunology , Dog Diseases/microbiology , Dogs , Female , Lymph Nodes/microbiology , Male , Tetracycline/administration & dosageSubject(s)
Adenocarcinoma/veterinary , Dog Diseases , Leukemoid Reaction/veterinary , Lung Neoplasms/veterinary , Pericardial Effusion/veterinary , Adenocarcinoma/complications , Adenocarcinoma/diagnostic imaging , Animals , Dog Diseases/diagnostic imaging , Dogs , Female , Leukemoid Reaction/etiology , Lung Neoplasms/complications , Lung Neoplasms/diagnostic imaging , Pericardial Effusion/diagnostic imaging , Pericardial Effusion/etiology , RadiographyABSTRACT
Eleven samples of Ottawa variety hard red winter wheat were inoculated with a standardized suspension of Salmonella montevideo. The contaminated wheat samples were placed in constant relative humidity (RH) chambers held at 25 C. Relative humidities were 7, 11, 22, 33, 43, 53, 62, 75, 84, 92, and 98%. Constant RH at 25 C was maintained with different saturated salt solutions in the sealed chambers. Periodic counts of viable S. montevideo cells per gram of wheat were made over a 28-week sampling period. Viable counts of S. montevideo on wheat held at 7, 11, and 22% RH decreased from an initial 10 cells/g of wheat to a final count of 10 cells/g in each sample. Samples stored at 33, 43, 53, and 62% RH decreased from 10 viable cells/g to 3.6 x 10, 10, 10, and 20 viable cells/g, respectively. No viable S. montevideo cells were detected in the samples held at 75, 84, 92, and 98% RH after 22, 16, 26, and 16 weeks, respectively.
ABSTRACT
Serological cross-reactions between certain streptococci and some serotypes of Streptococcus pneumoniae have been reported. These studies detail the serological cross-reactivity observed between hot HCl-extracted group b streptococcus type III (GBS III) antigens and S. pneumoniae type 14 (Pn 14) polysaccharide. Similar electrophoretic migration patterns of GBS III and Pn 14 were observed when either type-specific BGS III antisera or pneumococcal omniserum was utilized to precipitate these antigens. Both the GBS III antigen and the Pn 14 polysaccharide migrated toward the cathode, whereas all other pneumococcal polysaccharides migrated toward the anode. No cross-reactions were observed between GBS III antisera and the 11 other types of pneumococcal polysaccharides. Lines of identity were observed between type-specific GBS III antisera and monospecific Pn 14 antiserum with either GBS III antigens or purified Pn 14 polysaccharide. The cross-reacting antigens of GBS III and Pn 14 appear to be identical by immunodiffusion and immunoelectrophoresis.
Subject(s)
Antigens, Bacterial , Cross Reactions , Streptococcus agalactiae/immunology , Streptococcus pneumoniae/immunology , Immunodiffusion , ImmunoelectrophoresisABSTRACT
Miconazole, a broad-spectrum antimycotic agent with some antibacterial activity, has recently become available for experimental parenteral use in the United States. Its efficacy as an anticandidal drug was tested in adult Wistar rats. A previously established infectious dose of 5 x 10(6)Candida albicans was intravenously injected into 250- to 300-g animals. This dose was fatal to 95% (20/21) of placebo-treated control animals within the 2-week postinfection observation period. Only 4% (2/53) of rats receiving intramuscular miconazole treatment died. Miconazole therapy in Candida-infected rats at a dosage of 50 mg/kg per day resulted in 85% survival, and, although 100 mg/kg per day was 100% efficacious, it was a relatively large volume to give intramuscularly to a rat. Therefore, 75 mg/kg per day was used as a therapeutic dose, and it gave favorable results in this study. Histological examination of all placebo-treated animals revealed C. albicans and a marked inflammatory response in the kidney, brain, and heart. C. albicans organisms were observed to be very prominent in these tissues by using the Gomori methenamine silver stain, and were cultured from these organs. Miconazole-treated rats that were killed after surviving the 2-week observation period had minimal histopathological changes, and the organisms present did not exhibit the same staining characteristics, nor were they isolated like those in the placebo-treated group. Miconazole appears to be an efficacious drug for parenteral therapy, as demonstrated in this reproducible model of disseminated candidiasis in laboratory rats, and more extensive experimental studies are indicated.
Subject(s)
Candidiasis/drug therapy , Imidazoles/therapeutic use , Miconazole/therapeutic use , Animals , Candidiasis/microbiology , Candidiasis/pathology , Rats , Time FactorsABSTRACT
Sitophilus oryzae (L.), S. granarius (L.), Tribolium castaneum (Hbst.), Oryzaephilus surinamensis (L.), Rhyzopertha dominica (F.), Tenebroides mauritanicus (L.), and Cryptolestes pusillus (Schon.) transmitted Salmonella montevideo from wheat contaminated with 10(6) organisms/g to clean wheat. The insects were fed on the contaminated grain for 21 days and were then transferred to clean grain and allowed to feed for 21 days. They were subsequently transferred to two more samples of clean wheat. All species carried S. montevideo into the initial sample of clean wheat but not into a second or third sample. Progeny of the original insects that developed in the contaminated wheat exhibited less ability than the original adults to contaminate clean wheat. Data indicated that few S. montevideo could be carried by the stored-product insects in large masses of grain.
Subject(s)
Coleoptera , Food Contamination , Food Microbiology , Salmonella , Triticum , Agglutination Tests , Animals , Bacteriological Techniques , Indicators and Reagents , Salmonella/isolation & purificationABSTRACT
A micro-agglutination test for the antibodies to Brucella canis produced similar results to those obtained with the standard tube agglutination method in human and canine sera. The micromethod does provide an economical means of screening sera for the presence of antibodies.
Subject(s)
Agglutination Tests , Antibodies, Bacterial/analysis , Brucella/immunology , Animals , Brucellosis/diagnosis , Diagnosis, Differential , Dogs/immunology , Evaluation Studies as Topic , Guinea Pigs/immunology , Humans , Immune Sera , Immunologic Techniques , Rabbits/immunologyABSTRACT
Antisera directed against type-14 pneumococcus was opsonic for several strains of type-III group-B streptococcus. Furthermore, the polysaccharide antigen in the polyvalent pneumococcal vaccine reacted to form precipitation lines with antisera directed against type-14 pneumococcus and group-B streptococcus type III Immunisation with currently available pneumococcal vaccine may provide opsonic antibody against group-B streptococci and provide a method of preventing neonatal group-B streptococcal infections.
Subject(s)
Cross Reactions , Opsonin Proteins/immunology , Streptococcus agalactiae/immunology , Streptococcus pneumoniae/immunology , Animals , Antibodies, Bacterial/immunology , Antigens, Bacterial/immunology , Bacterial Vaccines/immunology , Blood Bactericidal Activity , Female , Humans , Immune Sera/immunology , Immunologic Deficiency Syndromes/prevention & control , Infant, Newborn , Infant, Newborn, Diseases/prevention & control , Neutrophils/immunology , Pneumococcal Infections/prevention & control , Precipitin Tests , Pregnancy , Pregnancy Complications, Infectious/prevention & control , Rabbits , Streptococcal Infections/prevention & controlABSTRACT
A blood culture technique that utilized small arterial blood samples or peripheral capillary blood was tested in beagle dogs and pig-tailed macaque monkeys. A bolus of 2.0 x 10(7)Escherichia coli (ATCC 25922) was injected intravenously into five animals of each species. Blood samples were taken before injection of the organisms and 10, 15, 20, 30, 60, and 120 min after injection. Arterial blood samples (2.0 and 0.2 ml) and peripheral capillary samples (0.14 ml) were taken at each sampling time. Pour plates were prepared from arterial blood for colony counts. All three blood sampling methods were equally effective in detecting sepsis when 10 or more organisms per ml of blood were present. Below this level, the 2.0-ml sample was more effective. Contamination of the peripheral sample with air or skin contaminants was a problem.