tetano
Editor, Senior Moderator
Viruses
. 2022 Jun 10;14(6):1263.
doi: 10.3390/v14061263.
Redesign and Validation of a Real-Time RT-PCR to Improve Surveillance for Avian Influenza Viruses of the H9 Subtype
Valentina Panzarin[SUP] 1 [/SUP], Sabrina Marciano[SUP] 1 [/SUP], Andrea Fortin[SUP] 1 [/SUP], Irene Brian[SUP] 1 [/SUP], Valeria D'Amico[SUP] 1 [/SUP], Federica Gobbo[SUP] 1 [/SUP], Francesco Bonfante[SUP] 1 [/SUP], Elisa Palumbo[SUP] 1 [/SUP], Yoshihiro Sakoda[SUP] 2 [/SUP], Kien Trung Le[SUP] 2 [/SUP], Duc-Huy Chu[SUP] 3 [/SUP], Ismaila Shittu[SUP] 4 [/SUP], Clement Meseko[SUP] 4 [/SUP], Abdoul Malick Haido[SUP] 5 [/SUP], Theophilus Odoom[SUP] 6 [/SUP], Mame Nahé Diouf[SUP] 7 [/SUP], Fidélia Djegui[SUP] 8 [/SUP], Mieke Steensels[SUP] 9 [/SUP], Calogero Terregino[SUP] 1 [/SUP], Isabella Monne[SUP] 1 [/SUP]
Affiliations
Abstract
Avian influenza viruses of the H9 subtype cause significant losses to poultry production in endemic regions of Asia, Africa and the Middle East and pose a risk to human health. The availability of reliable and updated diagnostic tools for H9 surveillance is thus paramount to ensure the prompt identification of this subtype. The genetic variability of H9 represents a challenge for molecular-based diagnostic methods and was the cause for suboptimal detection and false negatives during routine diagnostic monitoring. Starting from a dataset of sequences related to viruses of different origins and clades (Y439, Y280, G1), a bioinformatics workflow was optimized to extract relevant sequence data preparatory for oligonucleotides design. Analytical and diagnostic performances were assessed according to the OIE standards. To facilitate assay deployment, amplification conditions were optimized with different nucleic extraction systems and amplification kits. Performance of the new real-time RT-PCR was also evaluated in comparison to existing H9-detection methods, highlighting a significant improvement of sensitivity and inclusivity, in particular for G1 viruses. Data obtained suggest that the new assay has the potential to be employed under different settings and geographic areas for a sensitive detection of H9 viruses.
Keywords: H9Nx; avian influenza; molecular diagnosis; real-time RT-PCR; validation.
. 2022 Jun 10;14(6):1263.
doi: 10.3390/v14061263.
Redesign and Validation of a Real-Time RT-PCR to Improve Surveillance for Avian Influenza Viruses of the H9 Subtype
Valentina Panzarin[SUP] 1 [/SUP], Sabrina Marciano[SUP] 1 [/SUP], Andrea Fortin[SUP] 1 [/SUP], Irene Brian[SUP] 1 [/SUP], Valeria D'Amico[SUP] 1 [/SUP], Federica Gobbo[SUP] 1 [/SUP], Francesco Bonfante[SUP] 1 [/SUP], Elisa Palumbo[SUP] 1 [/SUP], Yoshihiro Sakoda[SUP] 2 [/SUP], Kien Trung Le[SUP] 2 [/SUP], Duc-Huy Chu[SUP] 3 [/SUP], Ismaila Shittu[SUP] 4 [/SUP], Clement Meseko[SUP] 4 [/SUP], Abdoul Malick Haido[SUP] 5 [/SUP], Theophilus Odoom[SUP] 6 [/SUP], Mame Nahé Diouf[SUP] 7 [/SUP], Fidélia Djegui[SUP] 8 [/SUP], Mieke Steensels[SUP] 9 [/SUP], Calogero Terregino[SUP] 1 [/SUP], Isabella Monne[SUP] 1 [/SUP]
Affiliations
- PMID: 35746734
- DOI: 10.3390/v14061263
Abstract
Avian influenza viruses of the H9 subtype cause significant losses to poultry production in endemic regions of Asia, Africa and the Middle East and pose a risk to human health. The availability of reliable and updated diagnostic tools for H9 surveillance is thus paramount to ensure the prompt identification of this subtype. The genetic variability of H9 represents a challenge for molecular-based diagnostic methods and was the cause for suboptimal detection and false negatives during routine diagnostic monitoring. Starting from a dataset of sequences related to viruses of different origins and clades (Y439, Y280, G1), a bioinformatics workflow was optimized to extract relevant sequence data preparatory for oligonucleotides design. Analytical and diagnostic performances were assessed according to the OIE standards. To facilitate assay deployment, amplification conditions were optimized with different nucleic extraction systems and amplification kits. Performance of the new real-time RT-PCR was also evaluated in comparison to existing H9-detection methods, highlighting a significant improvement of sensitivity and inclusivity, in particular for G1 viruses. Data obtained suggest that the new assay has the potential to be employed under different settings and geographic areas for a sensitive detection of H9 viruses.
Keywords: H9Nx; avian influenza; molecular diagnosis; real-time RT-PCR; validation.