AI Article Synopsis

  • - This study evaluates the effectiveness of different diagnostic techniques—Kato-Katz (KK), sodium nitrate (NaNO3) flotation (FF), and quantitative polymerase chain reaction (qPCR)—for detecting soil-transmitted helminths (STHs) in terms of egg recovery rates (ERR) and limits of detection (LOD) among infected human stool samples.
  • - Results showed that qPCR was significantly more sensitive, detecting as low as 5 eggs per gram (EPG) compared to 50 EPG for both KK and FF, with the latter also having lower ERRs overall.
  • - The findings suggest that qPCR's superior diagnostic capabilities warrant consideration for broader use in monitoring and assessing the effectiveness of STH control programs

Article Abstract

Background: Monitoring the success of soil-transmitted helminth (STH) control programs relies on accurate diagnosis and quantitative assessment of infection prevalence and intensity. As preventative chemotherapeutic program coverage for STH expands, the necessity of gaining insights into the relative or comparative sensitivities, in terms of limits of detection (LOD) and egg-recovery-rates (ERR) for microscopy and quantitative polymerase chain reaction qPCR-based diagnostic techniques becomes imperative to inform suitability for their intended use for large scale STH monitoring and treatment efficacy studies.

Methodology/principal Findings: The diagnostic performance in terms of ERR and LOD of the Kato-Katz (KK) thick smear technique, sodium nitrate (NaNO3) faecal floatation (FF) and qPCR for the accurate detection and enumeration of STH eggs were calculated and expressed in eggs per gram (EPG), by experimentally seeding parasite-free human faeces with Ascaris spp., Trichuris spp. and Necator americanus eggs representing low, medium and high intensity infections. The efficiency of NaNO3 flotation was also calculated over a range of specific gravities (SpGr) for the optimum recovery of STH eggs. FF of SpGr 1.30 recovered 62.7%, 11% and 8.7% more Trichuris spp., Necator americanus and Ascaris spp. eggs respectively, than the recommended SpGr of 1.20. All diagnostic methods demonstrated strong direct correlation to the intensity of seeded EPG. KK and FF (SpGr 1.30) resulted in significant lower ERRs compared to qPCR (p <0.05). qPCR demonstrated significantly (p <0.05) greater sensitivity with an ability to detect as little as 5 EPG for all three STH, compared to 50 EPG by KK and FF (SpGr 1.30).

Conclusions/significance: This study compares the diagnostic parameters in terms of LOD and ERRs of STHs for the KK, FF and qPCR. These results indicate that the diagnostic performance of qPCR assays should be considered by control programs in the phase that aims to seek confirmation of transmission break and cessation of preventive chemotherapy in low-transmission settings, in line with the control targets of the WHO neglected tropical diseases 2030 Roadmap.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153506PMC
http://dx.doi.org/10.1371/journal.pntd.0009395DOI Listing

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