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Comparative evaluation of fluorescent in situ hybridization and Giemsa microscopy with quantitative real-time PCR technique in detecting malaria parasites in a holoendemic region of Kenya.
Osoga, Joseph; Waitumbi, John; Guyah, Bernard; Sande, James; Arima, Cornel; Ayaya, Michael; Moseti, Caroline; Morang'a, Collins; Wahome, Martin; Achilla, Rachel; Awinda, George; Nyakoe, Nancy; Wanja, Elizabeth.
Affiliation
  • Osoga J; Malaria Diagnostics Center, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya. JOsoga@iavi.org.
  • Waitumbi J; Basic Sciences Laboratory, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Guyah B; Biomedical Sciences and Technology Department, School of Public Health and Community Development, Maseno University, Box Private Bag, Maseno, Kenya.
  • Sande J; Malaria Diagnostics Center, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Arima C; Malaria Diagnostics Center, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Ayaya M; Malaria Diagnostics Center, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Moseti C; Malaria Diagnostics Center, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Morang'a C; Malaria Diagnostics Center, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Wahome M; Basic Sciences Laboratory, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Achilla R; Malaria Diagnostics Center, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Awinda G; Basic Sciences Laboratory, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Nyakoe N; Basic Sciences Laboratory, Kenya Medical Research Institute/United States Army Medical Research Directorate-Kenya, Box 54, Kisumu, 40100, Kenya.
  • Wanja E; United States Army Medical Research Directorate-Armed Forces Research Institute of Medical Sciences, Bangkok, 10400, Thailand.
Malar J ; 16(1): 297, 2017 07 24.
Article in En | MEDLINE | ID: mdl-28738868
ABSTRACT

BACKGROUND:

Early and accurate diagnosis of malaria is important in treatment as well as in the clinical evaluation of drugs and vaccines. Evaluation of Giemsa-stained smears remains the gold standard for malaria diagnosis, although diagnostic errors and potential bias estimates of protective efficacy have been reported in practice. Plasmodium genus fluorescent in situ hybridization (P-Genus FISH) is a microscopy-based method that uses fluorescent labelled oligonucleotide probes targeted to pathogen specific ribosomal RNA fragments to detect malaria parasites in whole blood. This study sought to evaluate the diagnostic performance of P-Genus FISH alongside Giemsa microscopy compared to quantitative reverse transcription polymerase chain reaction (qRT-PCR) in a clinical setting.

METHOD:

Five hundred study participants were recruited prospectively and screened for Plasmodium parasites by P-Genus FISH assay, and Giemsa microscopy. The microscopic methods were performed by two trained personnel and were blinded, and if the results were discordant a third reading was performed as a tie breaker. The diagnostic performance of both methods was evaluated against qRT-PCR as a more sensitive method.

RESULTS:

The number of Plasmodium positive cases was 26.8% by P-Genus FISH, 33.2% by Giemsa microscopy, and 51.2% by qRT-PCR. The three methods had 46.8% concordant results with 61 positive cases and 173 negative cases. Compared to qRT-PCR the sensitivity and specificity of P-Genus FISH assay was 29.3 and 75.8%, respectively, while microscopy had 58.2 and 93.0% respectively. Microscopy had a higher positive and negative predictive values (89.8 and 68.0% respectively) compared to P-Genus FISH (56.0 and 50.5%). In overall, microscopy had a good measure of agreement (76%, k = 0.51) compared to P-Genus FISH (52%, k = 0.05).

CONCLUSION:

The diagnostic performance of P-Genus FISH was shown to be inferior to Giemsa microscopy in the clinical samples. This hinders the possible application of the method in the field despite the many advantages of the method especially diagnosis of low parasite density infections. The P-Genus assay has great potential but application of the method in clinical setting would rely on extensive training of microscopist and continuous proficiency testing.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmodium / In Situ Hybridization, Fluorescence / Real-Time Polymerase Chain Reaction / Malaria / Microscopy Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: Malar J Journal subject: MEDICINA TROPICAL Year: 2017 Type: Article Affiliation country: Kenya

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmodium / In Situ Hybridization, Fluorescence / Real-Time Polymerase Chain Reaction / Malaria / Microscopy Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Country/Region as subject: Africa Language: En Journal: Malar J Journal subject: MEDICINA TROPICAL Year: 2017 Type: Article Affiliation country: Kenya