A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted Helminths

The balance of expense and ease of use vs. specificity and sensitivity in diagnostic assays for helminth disease is an important consideration, with expense and ease often winning out in endemic areas where funds and sophisticated equipment may be scarce. In this review, we argue that molecular diag...

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Main Authors: Jessica R. Grant, Nils Pilotte, Steven A. Williams
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-09-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2019.00883/full
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spelling doaj-8c77054cb8d74b6498e93c1766f0bdea2020-11-24T21:26:40ZengFrontiers Media S.A.Frontiers in Genetics1664-80212019-09-011010.3389/fgene.2019.00883468253A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted HelminthsJessica R. Grant0Nils Pilotte1Nils Pilotte2Steven A. Williams3Steven A. Williams4Department of Biological Sciences, Smith College, Northampton, MA, United StatesDepartment of Biological Sciences, Smith College, Northampton, MA, United StatesMolecular and Cellular Biology Program, University of Massachusetts, Amherst, MA, United StatesDepartment of Biological Sciences, Smith College, Northampton, MA, United StatesMolecular and Cellular Biology Program, University of Massachusetts, Amherst, MA, United StatesThe balance of expense and ease of use vs. specificity and sensitivity in diagnostic assays for helminth disease is an important consideration, with expense and ease often winning out in endemic areas where funds and sophisticated equipment may be scarce. In this review, we argue that molecular diagnostics, specifically new assays that have been developed with the aid of next-generation sequence data and robust bioinformatic tools, more than make up for their expense with the benefit of a clear and precise assessment of the situation on the ground. Elimination efforts associated with the London Declaration and the World Health Organization (WHO) 2020 Roadmap have resulted in areas of low disease incidence and reduced infection burdens. An accurate assessment of infection levels is critical for determining where and when the programs can be successfully ended. Thus, more sensitive assays are needed in locations where elimination efforts are approaching a successful conclusion. Although microscopy or more general PCR targets have a role to play, they can mislead and cause study results to be confounded. Hyper-specific qPCR assays enable a more definitive assessment of the situation in the field, as well as of shifting dynamics and emerging diseases.https://www.frontiersin.org/article/10.3389/fgene.2019.00883/fullsoil-transmitted helminthmolecular diagnosticsDNA diagnosticspolymerase chain reaction (PCR)quantitative PCR
collection DOAJ
language English
format Article
sources DOAJ
author Jessica R. Grant
Nils Pilotte
Nils Pilotte
Steven A. Williams
Steven A. Williams
spellingShingle Jessica R. Grant
Nils Pilotte
Nils Pilotte
Steven A. Williams
Steven A. Williams
A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted Helminths
Frontiers in Genetics
soil-transmitted helminth
molecular diagnostics
DNA diagnostics
polymerase chain reaction (PCR)
quantitative PCR
author_facet Jessica R. Grant
Nils Pilotte
Nils Pilotte
Steven A. Williams
Steven A. Williams
author_sort Jessica R. Grant
title A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted Helminths
title_short A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted Helminths
title_full A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted Helminths
title_fullStr A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted Helminths
title_full_unstemmed A Case for Using Genomics and a Bioinformatics Pipeline to Develop Sensitive and Species-Specific PCR-Based Diagnostics for Soil-Transmitted Helminths
title_sort case for using genomics and a bioinformatics pipeline to develop sensitive and species-specific pcr-based diagnostics for soil-transmitted helminths
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2019-09-01
description The balance of expense and ease of use vs. specificity and sensitivity in diagnostic assays for helminth disease is an important consideration, with expense and ease often winning out in endemic areas where funds and sophisticated equipment may be scarce. In this review, we argue that molecular diagnostics, specifically new assays that have been developed with the aid of next-generation sequence data and robust bioinformatic tools, more than make up for their expense with the benefit of a clear and precise assessment of the situation on the ground. Elimination efforts associated with the London Declaration and the World Health Organization (WHO) 2020 Roadmap have resulted in areas of low disease incidence and reduced infection burdens. An accurate assessment of infection levels is critical for determining where and when the programs can be successfully ended. Thus, more sensitive assays are needed in locations where elimination efforts are approaching a successful conclusion. Although microscopy or more general PCR targets have a role to play, they can mislead and cause study results to be confounded. Hyper-specific qPCR assays enable a more definitive assessment of the situation in the field, as well as of shifting dynamics and emerging diseases.
topic soil-transmitted helminth
molecular diagnostics
DNA diagnostics
polymerase chain reaction (PCR)
quantitative PCR
url https://www.frontiersin.org/article/10.3389/fgene.2019.00883/full
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