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One-step PCR: A novel protocol for determination of pfhrp2 deletion status in Plasmodium falciparum.
- Source :
-
PloS one [PLoS One] 2020 Jul 23; Vol. 15 (7), pp. e0236369. Date of Electronic Publication: 2020 Jul 23 (Print Publication: 2020). - Publication Year :
- 2020
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Abstract
- Histidine-rich protein 2 (HRP2) detecting rapid diagnostic tests (RDTs) have played an important role in enabling prompt malaria diagnosis in remote locations. However, emergence of pfhrp2 deleted parasites is threatening the efficacy of RDTs, and the World Health Organization (WHO) has highlighted surveillance of these deletions as a priority. Nested PCR is used to confirm pfhrp2 deletion but is costly and laborious. Due to spurious amplification of paralogue pfhrp3, the identity of nested exon 1 PCR product must be confirmed by sequencing. Here we describe a new one-step PCR method for detection of pfhrp2. To determine sensitivity and specificity, all PCRs were performed in triplicate. Using photo-induced electron transfer (PET) PCR detecting 18srRNA as true positive, one-step had comparable sensitivity of 95.0% (88.7-98.4%) to nested exon 1, 99.0% (94.6-99.9%) and nested exon 2, 98.0% (93.0-99.8%), and comparable specificity 93.8% (69.8-99.8%) to nested exon 1 100.0% (79.4-100.0%) and nested exon 2, 100.0% (74.4-100.0%). Sequencing revealed that one step PCR does not amplify pfhrp3. Logistic regression models applied to measure the 95% level of detection of the one-step PCR in clinical isolates provided estimates of 133p/μL (95% confidence interval (CI): 3-793p/μL) for whole blood (WB) samples and 385p/μL (95% CI: 31-2133 p/μL) for dried blood spots (DBSs). When considering protocol attributes, the one-step PCR is less expensive, faster and more suitable for high throughput. In summary, we have developed a more accurate PCR method that may be ideal for the application of the WHO protocol for investigating pfhrp2 deletions in symptomatic individuals presenting to health care facilities.<br />Competing Interests: Authors Gireesh Subramaniam and Jasmine Padilla are employed by the Oak Ridge Institute for Science and Education (ORISE). ORISE provided support in the form of salary for authors GS and JP, but did not have any additional role role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Competing Interests statement: Authors Sophie Jones and Dhruviben Patel are employed by Williams Consulting LLC. There are no patents, products in development or marketed products to declare. This does not alter our adherence to all the PLOS ONE policies on sharing data and materials. Authors Gireesh Subramaniam and Jasmine Padilla are employed by the Oak Ridge Institute for Science and Education (ORISE). There are no patents, products in development or marketed products to declare. This does not alter our adherence to all the PLOS ONE policies on sharing data and materials.
- Subjects :
- Diagnostic Tests, Routine
Gene Deletion
Humans
Malaria, Falciparum genetics
Malaria, Falciparum parasitology
Plasmodium falciparum pathogenicity
Antigens, Protozoan genetics
Malaria, Falciparum diagnosis
Plasmodium falciparum genetics
Polymerase Chain Reaction methods
Protozoan Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 15
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 32702040
- Full Text :
- https://doi.org/10.1371/journal.pone.0236369