We report the development of three rapid, fully automated immunoassays allowing the differential diagnosis of acute viral hepatitis. These assays detect HBsAg, IgM antibody to hepatitis B core antigen (IgM anti-HBc) and IgM antibody to hepatitis A virus (IgM anti-HAV) using the IMx instrument system. All IMx assays were run in less than 45 minutes and all steps were fully automated including specimen dilution steps. Specimens from blood donors, diagnostic and hospital patients, and individuals with a variety of infectious and immune diseases were tested for IgM anti-HAV (n = 1473) or for IgM anti-HBc (n = 1606) or for HBsAg (n = 9700) by the IMx and commercially available EIA and RIA. Each IMx assay showed 99.8% agreement with current EIA. Reproducibility in all hepatitis IMx assays was significantly better than that observed with manual or semiautomated assays; within-run and between-run % CV ranged from 2.2 to 4.8 and 3.5 to 10.3 respectively. In 29 acute hepatitis B patients studied, HBsAg and IgM anti-HBc were detected in the first available patient bleed collected from 0 to 4 week from the onset of symptoms. IgM anti-HBc persisted at reactive levels in the IMx assay for 1 to 24 weeks (mean 12.1 +/- 5.3 weeks) after the patient presented with symptoms. In individuals exposed to hepatitis A, IgM anti-HAV was detectable by IMx by 40 days post exposure (average 33.5 days) and IgM had declined to unreactive levels in IMx for all patients by from 3 to 6 months post exposure. These data demonstrate the use of these rapid IMx assays for differentiation of acute hepatitis A and B.
Laboratory experiments were conducted in 55-L aquaria to evaluate the efficacy of the aquatic herbicide endothall and the fungal pathogen Mycoleptodiscus terrestris (Gerd.) Ostazeski, applied alone and in combination against hydrilla. Treatments included 0.25, 0.50, and 1.25 mg ae/L endothall, 100, 200, and 400 colony-forming units (CFU)/ml M. terrestris, simultaneous integrated treatments of 0.25, 0.50, and 1.25 endothall + 100 or 200 CFU/ml M. terrestris, sequential integrated treatments of 100 and 200 CFU/ml M. terrestris + 0.25 and 0.50 mg ae/L endothall, and untreated controls. By 42 d after treatment (DAT), all treatments had significantly reduced shoot biomass levels of hydrilla compared with the untreated controls. Combining the two lowest herbicide rates with M. terrestris provided better hydrilla control than either treatment alone. Based on these results, an outdoor mesocosm study was conducted to evaluate the efficacy and selectivity of endothall and the pathogen applied alone and in combination against hydrilla, Illinois pondweed, American pondweed, and vallisneria. Treatments included 0.25 and 0.50 mg ae/L endothall, 100 and 200 CFU/ml M. terrestris, integrated treatments of 0.25 and 0.50 mg ae/L endothall + 100 and 200 CFU/ml M. terrestris, and untreated controls. Unlike the laboratory results, none of the treatments controlled hydrilla 100%. The combined treatments worked better than either treatment applied alone. By 42 DAT, all the combined treatments except 0.25 mg ae/L endothall + 100 CFU/ml M. terrestris had reduced above-ground hydrilla biomass by ≥ 90% compared with the untreated controls. All nontarget species sustained varying amounts of injury from endothall and M. terrestris applied alone or in combination.
BackgroundIn 2009, a novel influenza virus (2009 pandemic influenza A (H1N1) virus (pH1N1)) caused significant disease in the United States. Most states, including Florida, experienced a large fall wave of disease from September through November, after which disease activity decreased substantially. We determined the prevalence of antibodies due to the pH1N1 virus in Florida after influenza activity had peaked and estimated the proportion of the population infected with pH1N1 virus during the pandemic.MethodsDuring November-December 2009, we collected leftover serum from a blood bank, a pediatric children's hospital and a pediatric outpatient clinic in Tampa Bay Florida. Serum was tested for pH1N1 virus antibodies using the hemagglutination-inhibition (HI) assay. HI titers ≥40 were considered seropositive. We adjusted seroprevalence results to account for previously established HI assay specificity and sensitivity and employed a simple statistical model to estimate the proportion of seropositivity due to pH1N1 virus infection and vaccination.ResultsDuring the study time period, the overall seroprevalence in Tampa Bay, Florida was 25%, increasing to 30% after adjusting for HI assay sensitivity and specificity. We estimated that 5.9% of the population had vaccine-induced seropositivity while 25% had seropositivity secondary to pH1N1 virus infection. The highest cumulative incidence of pH1N1 virus infection was among children aged 5–17 years (53%) and young adults aged 18–24 years (47%), while adults aged ≥50 years had the lowest cumulative incidence (11–13%) of pH1N1 virus infection.ConclusionsAfter the peak of the fall wave of the pandemic, an estimated one quarter of the Tampa Bay population had been infected with the pH1N1 virus. Consistent with epidemiologic trends observed during the pandemic, the highest burdens of disease were among school-aged children and young adults.
This technical note describes an outdoor mesocosm investigation conducted to evaluate the efficacy and selectivity of the herbicide fluridone (1-methyl-3-phenyl-5-[3-(trifluoromethyl)phenyl]-4(1H)-pyridinone) and the fungal pathogen Mycoleptodiscus terrestris (Gerd.) Ostazeski (Mt), applied alone and in combination with one another, against hydrilla (Hydrilla verticillata (L.f.) Royle), Eurasian watermilfoil (Myriophyllum spicatum L.), American pondweed (Potamogeton nodosus Poiret), and vallisneria (Vallisneria americana Michx.). Results of this research will determine the potential for integrating chemical and biological control tactics to improve the long-term management of nuisance aquatic weed species.
Growth chamber studies were conducted using 55-L aquariums to evaluate the efficacy of the herbicide triclopyr and the fungal pathogenMycoleptodiscus terrestris, applied alone and in combination against Eurasian watermilfoil. Treatments included 0.15, 0.40, and 1.50 mg acid equivalent (ae)/L triclopyr, 0.08, 0.16, and 0.32 ml/LM. terrestris, combinations of both agents at all rates, and an untreated control. Plants were exposed to all treatments for a 24-h contact time and plant biomass (shoot and roots) was recorded 6 wk after application. For both triclopyr andM. terrestrisapplied alone, plant control increased with treatment concentration. Compared with untreated plants, 1.50 mg/L triclopyr and 0.32 ml/LM. terrestrisreduced Eurasian watermilfoil by 100 and 91%, respectively. Lower doses of herbicide or pathogen were less effective and plant recovery was observed from surviving plant tissues (stems and root crowns). AlthoughM. terrestrisat 0.08 ml/L did not significantly reduce shoot or root biomass and 0.15 mg/L triclopyr provided only 53% control of plants, combining both agents at these rates reduced Eurasian watermilfoil by 90%. Results demonstrated that integrating low doses of triclopyr with an indigenous pathogen,M. terrestris, can improve control of Eurasian watermilfoil. Lower use rates of triclopyr would minimize impacts to sensitive nontarget vegetation, reduce application costs, and may minimize impacts of label-imposed use restrictions.
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