Validation of a Rapid Rabies Diagnostic Tool for Field Surveillance in Developing Countries

PLoS Negl Trop Dis. 2016 Oct 5;10(10):e0005010. doi: 10.1371/journal.pntd.0005010. eCollection 2016 Oct.

Abstract

Background: One root cause of the neglect of rabies is the lack of adequate diagnostic tests in the context of low income countries. A rapid, performance friendly and low cost method to detect rabies virus (RABV) in brain samples will contribute positively to surveillance and consequently to accurate data reporting, which is presently missing in the majority of rabies endemic countries.

Methodology/principal findings: We evaluated a rapid immunodiagnostic test (RIDT) in comparison with the standard fluorescent antibody test (FAT) and confirmed the detection of the viral RNA by real time reverse transcription polymerase chain reaction (RT-qPCR). Our analysis is a multicentre approach to validate the performance of the RIDT in both a field laboratory (N'Djamena, Chad) and an international reference laboratory (Institut Pasteur, Paris, France). In the field laboratory, 48 samples from dogs were tested and in the reference laboratory setting, a total of 73 samples was tested, representing a wide diversity of RABV in terms of animal species tested (13 different species), geographical origin of isolates with special emphasis on Africa, and different phylogenetic clades. Under reference laboratory conditions, specificity was 93.3% and sensitivity was 95.3% compared to the gold standard FAT test. Under field laboratory conditions, the RIDT yielded a higher reliability than the FAT test particularly on fresh and decomposed samples. Viral RNA was later extracted directly from the test filter paper and further used successfully for sequencing and genotyping.

Conclusion/significance: The RIDT shows excellent performance qualities both in regard to user friendliness and reliability of the result. In addition, the test cassettes can be used as a vehicle to ship viral RNA to reference laboratories for further laboratory confirmation of the diagnosis and for epidemiological investigations using nucleotide sequencing. The potential for satisfactory use in remote locations is therefore very high to improve the global knowledge of rabies epidemiology. However, we suggest some changes to the protocol, as well as careful further validation, before promotion and wider use.

Publication types

  • Validation Study

MeSH terms

  • Africa / epidemiology
  • Animals
  • Antigens, Viral / isolation & purification
  • Brain / virology
  • Chad / epidemiology
  • Developing Countries*
  • Dog Diseases / diagnosis*
  • Dog Diseases / epidemiology
  • Dog Diseases / virology
  • Dogs
  • Epidemiological Monitoring*
  • Fluorescent Antibody Technique, Direct
  • Genotype
  • Immunologic Tests / methods*
  • Laboratories
  • Phylogeny
  • RNA, Viral / isolation & purification
  • Rabies / diagnosis
  • Rabies / epidemiology
  • Rabies / veterinary*
  • Rabies / virology
  • Rabies virus / genetics
  • Rabies virus / isolation & purification*
  • Real-Time Polymerase Chain Reaction
  • Reproducibility of Results
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sensitivity and Specificity

Substances

  • Antigens, Viral
  • RNA, Viral

Grants and funding

This study has been kindly funded by the Federal Food Safety and Veterinary Office, Switzerland (project number 1.11.07). This study was also supported in part by Santé publique France (formerly Institut de Veille Sanitaire—InVS) and by the Direction Générale de la Santé, France. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.