Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era
Pneumococcal serotyping is required for epidemiological surveillance to guide vaccination strategy. DNA-based approaches are more affordable, but the combination of sequetyping and sequential conventional multiplex polymerase chain reaction (cmPCR) may complement one another. A total of 101 isolates...
Published in: | Pertanika Journal of Tropical Agricultural Science |
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Universiti Putra Malaysia
2023
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2-s2.0-85176752278 Rahman N.A.A.; Desa M.N.M.; Masri S.N.; Taib N.M.; Sulaiman N.; Dzaraly N.D.; Hazman H. Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era 2023 Pertanika Journal of Tropical Agricultural Science 46 4 10.47836/pjtas.46.4.10 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85176752278&doi=10.47836%2fpjtas.46.4.10&partnerID=40&md5=1b55ce3f5aaaaa4cfab39245f5abb4a8 Pneumococcal serotyping is required for epidemiological surveillance to guide vaccination strategy. DNA-based approaches are more affordable, but the combination of sequetyping and sequential conventional multiplex polymerase chain reaction (cmPCR) may complement one another. A total of 101 isolates were subjected to sequetyping and sequential cmPCR following previously published protocols, and the outputs were compared. The sequetyping method determined up to the serotype level for 99 isolates (98%). On the other hand, the sequential cmPCR technique identified 91 isolates (90.1%), with 63 of them (62.4%) up to the serotype level. Sequetyping generated discrete serotypes for 6A/B, 11A/D, 15A/F, and 15B/C as 6A (n = 11), 6B (n = 10), 11A (n = 5), 15C (n = 1), and 15A (n = 1). In conclusion, the cpsB gene sequetyping method produced a comparable output with sequential cmPCR, further discriminating some sub-serogroups among the isolate collection. © 2023 Universiti Putra Malaysia. All rights reserved. Universiti Putra Malaysia 15113701 English Article All Open Access; Gold Open Access |
author |
Rahman N.A.A.; Desa M.N.M.; Masri S.N.; Taib N.M.; Sulaiman N.; Dzaraly N.D.; Hazman H. |
spellingShingle |
Rahman N.A.A.; Desa M.N.M.; Masri S.N.; Taib N.M.; Sulaiman N.; Dzaraly N.D.; Hazman H. Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era |
author_facet |
Rahman N.A.A.; Desa M.N.M.; Masri S.N.; Taib N.M.; Sulaiman N.; Dzaraly N.D.; Hazman H. |
author_sort |
Rahman N.A.A.; Desa M.N.M.; Masri S.N.; Taib N.M.; Sulaiman N.; Dzaraly N.D.; Hazman H. |
title |
Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era |
title_short |
Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era |
title_full |
Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era |
title_fullStr |
Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era |
title_full_unstemmed |
Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era |
title_sort |
Determination of Pneumococcal Serotypes by Sequetyping and Sequential Conventional Multiplex PCR in the Vaccine Era |
publishDate |
2023 |
container_title |
Pertanika Journal of Tropical Agricultural Science |
container_volume |
46 |
container_issue |
4 |
doi_str_mv |
10.47836/pjtas.46.4.10 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85176752278&doi=10.47836%2fpjtas.46.4.10&partnerID=40&md5=1b55ce3f5aaaaa4cfab39245f5abb4a8 |
description |
Pneumococcal serotyping is required for epidemiological surveillance to guide vaccination strategy. DNA-based approaches are more affordable, but the combination of sequetyping and sequential conventional multiplex polymerase chain reaction (cmPCR) may complement one another. A total of 101 isolates were subjected to sequetyping and sequential cmPCR following previously published protocols, and the outputs were compared. The sequetyping method determined up to the serotype level for 99 isolates (98%). On the other hand, the sequential cmPCR technique identified 91 isolates (90.1%), with 63 of them (62.4%) up to the serotype level. Sequetyping generated discrete serotypes for 6A/B, 11A/D, 15A/F, and 15B/C as 6A (n = 11), 6B (n = 10), 11A (n = 5), 15C (n = 1), and 15A (n = 1). In conclusion, the cpsB gene sequetyping method produced a comparable output with sequential cmPCR, further discriminating some sub-serogroups among the isolate collection. © 2023 Universiti Putra Malaysia. All rights reserved. |
publisher |
Universiti Putra Malaysia |
issn |
15113701 |
language |
English |
format |
Article |
accesstype |
All Open Access; Gold Open Access |
record_format |
scopus |
collection |
Scopus |
_version_ |
1809678020849434624 |