Comparative study of HA and HNB staining RT-LAMP assays for peste des petits ruminants virus detection in West African Dwarf goats

• Published in: Tropical animal health and production 2023-12, Vol.55 (6), p.356-356, Article 356
• Main Authors: Muritala, Ismaila, Bemji, Martha N., Ozoje, Michael O., Ajayi, Olusola L., Oluwayinka, Eniope B., Sonibare, Adekayode O., James, Ikechukwu J., Ibeagha-Awemu, Eveline M.
• Format: Article
• Language: English
• Subjects: Animals; Assaying; Biomedical and Life Sciences; Comparative studies; Developing countries; Disease; Economic impact; Eradication; Goat Diseases - epidemiology; Goats; Hemagglutination; Infections; Laboratories; LDCs; Life Sciences; Mortality; Naphthols; Peste des petits ruminants; Peste-des-Petits-Ruminants - epidemiology; Peste-des-petits-ruminants virus; Phenotyping; Pneumonia; Regular Articles; Reverse transcription; Rinderpest; Sensitivity; Staining; Staining and Labeling - veterinary; The Gordon Scott Collection; Veterinary colleges; Veterinary medicine; Veterinary Medicine/Veterinary Science; Viral infections; Viruses; Zoology
• ISSN: 0049-4747; 1573-7438
• DOI: 10.1007/s11250-023-03747-5

Peste des petits ruminants (PPR) cause severe economic losses to many countries of the world where the disease is endemic. It has been targeted for global eradication by 2030 following the successful eradication of rinderpest in 2011. The proposed eradication program would benefit from efficient and relatively reliable diagnostic tools for early PPR virus (PPRV) detection. A total of 33 eight to 12 months old West African Dwarf (WAD) goats were used. Nineteen goats infected by commingling with two PPR virus–positive animals formed the infected group (PPRV-infected goats) while 14 non-infected goats formed the control group (CTG). The suitability of hydroxyl naphthol blue (HNB) staining of reverse transcription loop–mediated isothermal amplification (RT-LAMP) and haemagglutination (HA) assays was compared for their sensitivity to detect the PPRV in PPRV-infected goats and non-infected CTG. PPR disease severity in WAD goats at different days post infection (dpi) was evaluated by clinical scoring and haemagglutination titre (HAT). HNB staining RT-LAMP reaction and HA showed sensitivities of 100% and 73.68%, respectively, for PPRV detection. Expression of PPR clinical signs began from 3 dpi, attained peak at 5 dpi, thereafter showed irregular patterns till 24 dpi. Evaluation of HAT in PPRV-infected goats at 12 dpi ranged from 2 to 64 haemagglutination units (HAU), while CTG goats had 0 HAU. In conclusion, HA could be a good tool for rapid diagnosis of PPRV in a developing country setting. However, HNB staining RT-LAMP assay demonstrated high sensitivity for accurate diagnoses of PPRV and as an important diagnostic tool when precise phenotyping is desired.