Skip to main content
BMC Genomics logoLink to BMC Genomics
. 2021 Mar 26;22:219. doi: 10.1186/s12864-021-07444-1

Correction to: Identification of highly conserved, serotype-specific dengue virus sequences: implications for vaccine design

Li Chuin Chong 1, Asif M Khan 1,
PMCID: PMC7995763  PMID: 33771112

Correction to: BMC Genomics 20, 921 (2019)

https://doi.org/10.1186/s12864-019-6311-z

Following publication of the original article [1], the authors noted that some of the changes suggested during the proofing stage were missed. The authors highlight these below and includes a few additional changes for clarity:

1) In the background part of the Abstract section:

The published version of the sentence: “The former aims to limit the number of possible cross-reactive epitope variants in the population, while the latter aims to limit the cross-reactivity between the serotypes to favour a serotype-specific response.” should have been as follows: “The former pan-DENV sequence approach aims to limit the number of possible cross-reactive epitope variants in the population, while the current HCSS sequence approach aims to limit the cross-reactivity between the serotypes to favour a serotype-specific response.”

2) In the result part of the Abstract section:

The published version of the sentence: “Concatenating these resulted in a total of 337 HCSS sequences. DENV4 had the most number of HCSS nonamers; NS5, NS3 and E proteins had among the highest, with none in the C and only one in prM.” should have been as follows: “DENV4 had the most number of HCSS nonamers; NS5, NS3 and E proteins had among the highest across the serotypes, with the lowest in the C. Concatenating the 2,321 nonamers resulted in a total of 337 HCSS sequences.”

3) In the result part of the Abstract section:

The published version of the sentence: “HCSS sequences of a given serotype showed significant amino acid difference to all the variants of the other serotypes, supporting the notion of serotype-specificity.” should have been as follows: “Observation of select HCSS sequences of a given serotype showed significant amino acid difference to the variants of the other serotypes, supporting the notion of serotype-specificity.”

4) In the Introduction section:

The published version of the sentence: “The pan-DENV sequences may be of utility in the design of tetravalent vaccine to avoid regions of T-cell immunity that are highly variable across the four serotypes, except when they are serotype-specific [33, 36].” should have been as follows: “The pan-DENV sequences may be of utility in the design of a vaccine against the four serotypes to avoid regions of T-cell immunity that are highly variable across the serotypes, except perhaps when they are serotype-specific [33, 36].”

5) In the Method section:

The published version of the sentence: “The blast parameters (E-value less than 0.05) were used to evaluate the significance of the hits and select the sequences for each serotype protein.” should have been as follows: “The blast parameters (E-value less than 0.05, among others) were used to evaluate the significance of the hits and select the sequences for each serotype protein.”

6) In Table 3:

Table 3.

Nonamer positions depicting amino acid differences between an HCSS nonamer and the corresponding variants, within and between the serotypes. Only positions of mutual information value of 1 and low entropy values are shown. The reference HCSS nonamers shown at the top were arbitrarily chosen (match to DENV2), and additional HCSS nonamers, if present, are shown in bold. Data for two additional positions are shown in Supplementary Table 4.

Protein | Entropy Value NS1 | 0.12 NS2a | 0.11
HCSS Reference 146 NRAWNSLEV 154 202 LNPTAIFLT 210
DENV1 146 Q....IW.. 154 202 CK.LTM..I 210
146 Q....VW.. 154 202 CK.LPM..I 210
146 L....IW.. 154 202 CK.LTML.I 210
146 H....IW.. 154 202 CK.LTM.FI 210
146 Q....IWK. 154 202 CK.LTMY.I 210
146 Q..S.IW.. 154 202 CK.L.M..I 210
146 Q....IW.G 154 202 CK.L.ML.I 210
146 Q....I... 154 202 CK.LTM..V 210
146 Q...TIW.. 154 202 CK.STM..I 210
202 C..LTM..I 210
202 SK.LTM..I 210
202 CK.LTMYFI 210
202 CKTLTM..I 210
DENV2 146 ......... 154 202 ......... 210
146 S........ 154 202 .......I. 210
146 .......K. 154 202 .S....... 210
146 .......KG 154 202 ......L.. 210
146 ..T.D.... 154 202 ......YF. 210
146 .......KL 154
DENV3 146 S....VW.. 154 202 VP.LPL.IF 210
146 A....VW.. 154 202 VP.LPLLIF 210
146 L....VW.. 154 202 IP.LPL.IF 210
146 S..L.VW.. 154 202 .P.LPL.IF 210
202 VQ.LPL.IF 210
202 VS.LPL.IF 210
202 VP.SPL.IF 210
202 VPSLPL.IF 210
202 AQ.LPL.IF 210
DENV4 146 R........ 154 202 AQALPVY.M 210
146 R....F... 154
146 R.....F.. 154
146 R....FF.. 154

The published version of Table 3 contained formatting errors. The corrected version is as below.

Reference

  • 1.Chong LC, Khan AM. Identification of highly conserved, serotype-specific dengue virus sequences: implications for vaccine design. BMC Genomics. 2019;20:921. doi: 10.1186/s12864-019-6311-z. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from BMC Genomics are provided here courtesy of BMC

RESOURCES