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1.
Emerg Infect Dis ; 30(2): 245-254, 2024 02.
Article in English | MEDLINE | ID: mdl-38270128

ABSTRACT

During January-August 2021, the Community Prevalence of SARS-CoV-2 Study used time/location sampling to recruit a cross-sectional, population-based cohort to estimate SARS-CoV-2 seroprevalence and nasal swab sample PCR positivity across 15 US communities. Survey-weighted estimates of SARS-CoV-2 infection and vaccine willingness among participants at each site were compared within demographic groups by using linear regression models with inverse variance weighting. Among 22,284 persons >2 months of age and older, median prevalence of infection (prior, active, or both) was 12.9% across sites and similar across age groups. Within each site, average prevalence of infection was 3 percentage points higher for Black than White persons and average vaccine willingness was 10 percentage points lower for Black than White persons and 7 percentage points lower for Black persons than for persons in other racial groups. The higher prevalence of SARS-CoV-2 infection among groups with lower vaccine willingness highlights the disparate effect of COVID-19 and its complications.


Subject(s)
COVID-19 , Vaccines , Adult , Child , Humans , COVID-19/epidemiology , SARS-CoV-2 , Cross-Sectional Studies , Prevalence , Seroepidemiologic Studies
2.
Dalton Trans ; 53(20): 8584-8592, 2024 May 21.
Article in English | MEDLINE | ID: mdl-38687325

ABSTRACT

The impressive photoluminescence properties of all inorganic cesium lead halide perovskite quantum dots (PeQDs) make them highly intriguing for fluorescence chemosensor applications. Herein, a ratiometric dual emitting perovskite-based sensor was designed by synthesizing fluorescent CsPbBr3 PeQDs in situ within a matrix of Eu-BDC (Eu(III) benzene-1,4-dicarboxylate). The results presented here establish the suggested sensor's quick and selective turn-on PL response to volatile primary aliphatic amine derivatives. In the presence of amines, the designed CsPbBr3/Eu-BDC sensor exhibits an enhancement of the PL signal of CsPbBr3 at 518 nm and the Eu-BDC signal at 615 nm served as a standard for constructing the ratiometric sensing system. Thereby, a visual color change from red to green was observed with the incremental addition of methylamine to the probe. A low detection limit of 0.083 ppm was determined for methylamine. In both the solution and vapor phases, this ratiometric sensor responds to a variety of primary aliphatic amines with very quick and strong fluorescence. Moreover, the sensor was effectively used for monitoring meat spoilage owing to the emission of biogenic amine vapor from meat products.

3.
Microbiol Spectr ; : e0030724, 2024 Jul 09.
Article in English | MEDLINE | ID: mdl-38980027

ABSTRACT

Detection of HIV infection may be challenging in persons using long-acting cabotegravir (CAB-LA) pre-exposure prophylaxis (PrEP) due to viral suppression and reduced/delayed antibody production. We evaluated two point-of-care tests for detecting HIV infection in persons who received CAB-LA in the HPTN 083 trial. Samples were obtained from 12 participants who received CAB-LA and had delayed detection of HIV infection using HIV rapid tests and an antigen/antibody test (52 plasma samples; 18 dried blood spot [DBS] samples). Plasma samples were tested with the Xpert HIV-1 Viral Load XC test (Xpert VL-XC); DBS samples were tested with the total nucleic acid Xpert HIV-1 Qual XC test (Xpert Qual-XC). Results from these assays were compared to results from three reference, laboratory-based, plasma RNA assays (Aptima HIV-1 Qualitative assay [Aptima Qual]; Aptima HIV-1 Quant DX Assay [Aptima Quant]; cobas HIV-1/HIV-2 Qualitative Test [cobas]). HIV RNA was detected with all four plasma assays for all samples with viral loads (VLs) ≥ 200 copies/mL; the number of samples with VLs < 200 copies/mL with HIV RNA detected was: Xpert VL-XC: 19/26 (73.1%); Aptima Qual: 17/26 (65.4%); Aptima Quant: 17/26 (65.4%); and cobas: 12/21 (57.1%). The Xpert Qual-XC assay was positive for all DBS samples with VLs ≥ 200 copies/mL and 1/10 DBS with VLs < 200 copies/mL. The performance of the Xpert VL-XC assay was comparable to the reference assays for detecting HIV infection in these cases. The Xpert Qual-XC assay was less sensitive than plasma-based HIV RNA assays for detecting HIV in the setting of CAB-LA PrEP. IMPORTANCE: HIV RNA assays can detect HIV infections earlier than HIV rapid tests or Ag/Ab tests in persons using CAB-LA PrEP. Earlier HIV diagnosis could allow for earlier treatment initiation and reduced risk of INSTI resistance. POC tests may help detect HIV infection before CAB-LA administration and may be more accessible than laboratory-based assays in some settings. In this study, the POC Xpert VL-XC assay detected HIV RNA in most samples from individuals who received CAB-LA PrEP and had delayed detection of HIV infection with HIV rapid tests and an Ag/Ab test. The performance of this assay was similar to laboratory-based HIV RNA assays in this cohort. The POC Xpert Qual-XC assay detects both HIV RNA and DNA, with a higher viral load cutoff for RNA detection. This assay was negative for most lower viral load samples and did not offer an advantage for HIV screening in persons using CAB-LA PrEP.

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