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Background: COVID-19 pandemic interrupted routine care for individuals living with HIV, putting them at risk of becoming virologically unsuppressed and ill. Often they are at high risk for exposure to SARS-CoV-2 infection and severe disease once infected. For this population, it is urgent to closely monitor HIV plasma viral load ( ) and screen for SARS-COV-2 infection.
Method: We have developed a non-proprietary method to isolate RNA from plasma, nasal secretions ( ), or both. HIV, SARS-CoV-2, and human RP targets in extracted RNA are then RT-qPCR to estimate the VL and classify HIV/SARS-CoV-2 status ( . ., HIV as VL failure or suppressed; SARS-CoV-2 as positive, presumptive positive, negative, or indeterminate). We evaluated this workflow on 133 clinical specimens: 40 plasma specimens (30 HIV-seropositive), 67 NS specimens (31 SARS-CoV-2-positive), and 26 pooled plasma/NS specimens (26 HIV-positive with 10 SARS-CoV-2-positive), and compared the results obtained using the in-house extraction to those using a commercial extraction kit.
Results: In-house extraction had a detection limit of 200-copies/mL for HIV and 100-copies/mL for SARS-CoV-2. In-house and commercial methods yielded positively correlated HIV VL (R : 0.98 for contrived samples; 0.81 for seropositive plasma). SARS-CoV-2 detection had 100% concordant classifications in contrived samples, and in clinical NS extracted by in-house method, excluding indeterminate results, was 95% concordant (25 positives, 6 presumptive positives, and 31 negatives) to those using the commercial method. Analysis of pooled plasma/NS showed R of 0.91 (contrived samples) and 0.71 (clinical specimens) for HIV VL correlations obtained by both extraction methods, while SARS-CoV-2 detection showed 100% concordance in contrived and clinical specimens.
Interpretation: Our low-cost workflow for molecular testing of HIV and SARS-CoV-2 could serve as an alternative to current standard assays for laboratories in low-resource settings.
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http://dx.doi.org/10.1101/2021.08.18.21256786 | DOI Listing |
Background: To improve the molecular diagnostic yield for Aspergillus spp. from respiratory samples, we developed and evaluated a new DNA extraction method directly from respiratory samples combined with in-house Aspergillus real-time PCR.
Methods: We developed a method using beads and resin, where a sample is centrifuged to separate the supernatant and pellet.
J Clin Microbiol
August 2025
The Atlanta Center for Microsystems-Engineered Point-of-Care Technologies, Atlanta, Georgia, USA.
Highly pathogenic avian influenza (HPAI) A(H5N1) clade 2.3.4.
View Article and Find Full Text PDFJCO Clin Cancer Inform
August 2025
Biofidelity Ltd, Cambridge, United Kingdom.
Purpose: Aspyre Lung is a targeted biomarker panel of 114 genomic variants across 11 guideline-recommended genes with simultaneous DNA and RNA for non-small cell lung cancer (NSCLC). In this study, we developed a machine learning algorithm to interpret fluorescence data outputs from Aspyre Lung, enabling the assay to be applied to both plasma and tissue samples.
Materials And Methods: Data for model training and testing were generated from over 13,500 DNA and RNA contrived samples, with variants spiked in at a variant allele frequency (VAF) of 0.
Hum Vaccin Immunother
December 2025
Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
A standardized multiplex immunoassay (MIA) to quantify group B (GBS) anti-capsular polysaccharide (CPS) IgG serum concentrations was adopted by the roup B Streptococcal ssay andardizati (GASTON) consortium as a standardized serological assay with the most immediate applications for facilitating the licensure of GBS vaccines. However, dried blood spot (DBS) samples offer advantages for immunological studies, including cost-effectiveness, ease of transport, and storage. To determine suitability of DBS as an alternative sample matrix to serum in MIA, a contrived GBS seropositive panel, including matched DBS and serum samples, was prepared using established methods.
View Article and Find Full Text PDFFront Cell Infect Microbiol
August 2025
Unit of Microbiology, The Great Romagna Hub Laboratory, Pievesestina, Italy.
Introduction: Bloodstream infections (BSIs) represent a significant public health concern, characterized by the presence of pathogens in the bloodstream, leading to serious conditions. Between 30 and 40% of BSIs evolve in sepsis, characterized by a life-threatening organ dysfunction and accompanied by a strong or dysregulated systemic immune or inflammatory response. A timely and accurate diagnosis of BSIs is crucial for ensuring effective management and treatment of critically ill patients.
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