Large-volume RT-LAMP enables extraction-free amplification of HIV RNA from fingerstick plasma

• Published in: Analytica chimica acta 2024-06, Vol.1307, p.342560-342560, Article 342560
• Main Authors: Wang, Qin, Gilligan-Steinberg, Shane D., Kim, Wookyeom, Kline, Enos C., Hull, Ian T., Lai, James J., Lutz, Barry R.
• Format: Article
• Language: English
• Subjects: Extraction-free amplification; Fingerstick blood; HIV Infections - blood; HIV Infections - diagnosis; HIV Infections - virology; HIV-1 - genetics; HIV-1 - isolation & purification; Humans; Inhibitor; Isothermal amplification; Limit of Detection; Molecular Diagnostic Techniques; Nucleic Acid Amplification Techniques - methods; Point-of-care; Reaction volume; RNA, Viral - blood
• ISSN: 0003-2670; 1873-4324
• DOI: 10.1016/j.aca.2024.342560

Point-of-care (POC) nucleic acid amplification tests (NAAT) can significantly expand testing coverage, which is critical for infectious disease diagnostics and monitoring. The development of various isothermal amplification techniques greatly simplifies NAATs, but the cumbersome nucleic acid extraction step remains a bottleneck for the POC. Alternatively, extraction-free amplification, where crude samples are directly added into the assay, substantially simplifies the workflow. However, sample dilution is often needed in extraction-free amplification to reduce assay inhibition from sample matrices. Since NAATs are typically run at small volumes around 20 μL, the input sample quantity is therefore limited, resulting in an inevitable sensitivity loss. Here we explore the potential to perform isothermal amplification in larger reaction volumes to accommodate larger sample quantities, thereby improving sensitivity in extraction-free amplification. We demonstrated the approach by developing large-volume reverse transcription loop-mediated isothermal amplification (RT-LAMP) for HIV RNA detection from fingerstick plasma. We found that LAMP at reaction volumes up to 1 mL maintained the same performance. We then identified plasma dilution conditions needed to maintain the limit of detection in RT-LAMP. Subsequently, using inactivated HIV virus, we showed the successful detection of 24 HIV RNA copies in a 500 μL RT-LAMP reaction in the presence of 20 μL plasma (fingerstick volumes), translating to a viral load of 1200 copies per mL. To reduce the increased reagent cost with expanded reaction volumes, we further identified lower-cost reagents with maintained assay performance. Moreover, we showed that large-volume LAMP, compared to 20 μL reactions, could tolerate higher concentrations of various inhibitors in the sample, such as albumin and GuSCN. NAATs are conventionally conducted at small reaction volumes. Here we demonstrated that LAMP can be run at large reaction volumes (over 100 μL) with maintained assay performance, allowing sample inhibition to be mitigated while accommodating larger sample quantities. The same strategy of expanding reaction volumes could be applied to other isothermal amplification methods and various POC applications, to streamline test workflows and/or improve assay sensitivity. [Display omitted] •LAMP at volumes up to 1 mL maintains the same performance as 20 μL reactions.•RT-LAMP shows the same amplification LoD with 4% plasma in the rea