Evidence map›Paper›PMID 36910181›Full record

ArticleFrontiers in microbiology2023

Comparative mutational analysis of the Zika virus genome from different geographical locations and its effect on the efficacy of Zika virus-specific neutralizing antibodies.

Abdul Aziz, Muhammad Suleman, Abdullah Shah, Ata Ullah, Farooq Rashid, Sikandar Khan, Arshad Iqbal, Sisi Luo, Liji Xie, Zhixun Xie

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. An Overview of Zika Virus and Zika Virus Induced Neuropathies.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Abdul AzizMolecular Biology Research Center, School of Life Sciences, Central South University, Changsha, China.
Muhammad SulemanCentre for Biotechnology and Microbiology, University of Swat, Mingora, Pakistan.
Abdullah ShahDepartment of Biotechnology, Shaheed Benazir Bhutto University, Upper Dir, Pakistan.
Ata UllahNew Cross Hospital, The Royal Wolverhampton NHS Trust, Wolverhampton, United Kingdom.
Farooq RashidDivision of Infectious Diseases, Chongqing Public Health Medical Center, Chongqing, China.
Sikandar KhanDepartment of Biotechnology, Shaheed Benazir Bhutto University, Upper Dir, Pakistan.
Arshad IqbalCentre for Biotechnology and Microbiology, University of Swat, Mingora, Pakistan.
Sisi LuoDepartment of Biotechnology, Guangxi Veterinary Research Institute, Nanning, China.
Liji XieDepartment of Biotechnology, Guangxi Veterinary Research Institute, Nanning, China.
Zhixun XieDepartment of Biotechnology, Guangxi Veterinary Research Institute, Nanning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Zika virus (ZIKV), which originated in Africa, has become a significant global health threat. It is an RNA virus that continues to mutate and accumulate multiple mutations in its genome. These genetic changes can impact the virus's ability to infect, cause disease, spread, evade the immune system, and drug resistance. In this study genome-wide analysis of 175 ZIKV isolates deposited at the National Center for Biotechnology Information (NCBI), was carried out. The comprehensive mutational analysis of these isolates was carried out by DNASTAR and Clustal W software, which revealed 257 different substitutions at the proteome level in different proteins when compared to the reference sequence (KX369547.1). The substitutions were capsid (17/257), preM (17/257), envelope (44/257), NS1 (34/257), NS2A (30/257), NS2B (11/257), NS3 (37/257), NS4A (6/257), 2K (1/257), NS4B (15/257), and NS5 (56/257). Based on the coexisting mutational analysis, the MN025403.1 isolate from Guinea was identified as having 111 substitutions in proteins and 6 deletions. The effect of coexisting/reoccurring mutations on the structural stability of each protein was also determined by I-mutant and MUpro online servers. Furthermore, molecular docking and simulation results showed that the coexisting mutations (I317V and E393D) in Domain III (DIII) of the envelope protein enhanced the bonding network with ZIKV-specific neutralizing antibodies. This study, therefore, highlighted the rapid accumulation of different substitutions in various ZIKV proteins circulating in different geographical regions of the world. Surveillance of such mutations in the respective proteins will be helpful in the development of effective ZIKV vaccines and neutralizing antibody engineering.

Indexed as

Guillain–Barré syndromeMD simulationsmutational analysisneutralizing antibodiesZika virus

Identifiers

PMID36910181
PMCPMC9992208

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.