Evidence map›Paper›PMID 36295517›Full record

ArticleMedicina (Kaunas, Lithuania)2022

Designing mRNA- and Peptide-Based Vaccine Construct against Emerging Multidrug-Resistant

Muhammad Naveed, Jawad-Ul Hassan, Muneeb Ahmad, Nida Naeem, Muhammad Saad Mughal, Ali A Rabaan, Mohammed Aljeldah, Basim R Al Shammari, Mohammed Alissa, Amal A Sabour and 5 more

Open access · goldAbstract read
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
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

8 citing papers in PubMed, 14 citations in OpenAlex.

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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

15 authors at 9 institutions in 3 countries.

Muhammad NaveedDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore 54590, Pakistan.ORCID 0000-0002-4333-8226
Jawad-Ul HassanDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore 54590, Pakistan.
Muneeb AhmadDepartment of Medical Education, Rawalpindi Medical University, Rawalpindi 46000, Pakistan.
Nida NaeemDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore 54590, Pakistan.ORCID 0000-0003-3187-2779
Muhammad Saad MughalDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore 54590, Pakistan.ORCID 0000-0001-7461-6826
Ali A RabaanMolecular Diagnostic Laboratory, Johns Hopkins Aramco Healthcare, Dhahran 31311, Saudi Arabia.ORCID 0000-0002-6774-9847
Mohammed AljeldahDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hafr Al Batin, Hafr Al Batin 39831, Saudi Arabia.ORCID 0000-0001-5335-2809
Basim R Al ShammariDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hafr Al Batin, Hafr Al Batin 39831, Saudi Arabia.ORCID 0000-0002-3522-0607
Mohammed AlissaDepartment of Medical Laboratory Sciences, College of Applied Medical Sciences, Prince Sattam bin Abdulaziz University, Al-Kharj 11942, Saudi Arabia.ORCID 0000-0002-4045-0810
Amal A SabourDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Rana A AlaeqDepartment of Medical Laboratories Technology, Faculty of Applied Medical Science, Taibah University, Al Madinah Al Munawarh 42353, Saudi Arabia.ORCID 0000-0002-4080-5941
Maha A AlshiekheidDepartment of Botany and Microbiology, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Safaa A TurkistaniDepartment of Medical Laboratory, Fakeeh College for Medical Science, Jeddah 21134, Saudi Arabia.ORCID 0000-0002-8607-5251
Abdirahman Hussein ElmiDepartment of Medical Microbiology and Parasitology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian 16150, Malaysia.
Naveed AhmedDepartment of Biotechnology, Faculty of Science and Technology, University of Central Punjab, Lahore 54590, Pakistan.ORCID 0000-0003-1504-1705
University of Central Punjab · PKKing Saud University · SAUniversiti Sains Malaysia · MYUniversity of Hafr Al-Batin · SAAlfaisal University · SAPrince Sattam Bin Abdulaziz University · SARawalpindi Medical University · PKSoliman Fakeeh Hospital · SATaibah University · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Citrobacter freundii (C. freundii) is an emerging and opportunistic Gram-negative bacteria of the human gastrointestinal tract associated with nosocomial and severe respiratory tract infections. It has also been associated with pneumonia, bloodstream, and urinary tract infections. Intrinsic and adaptive virulence characteristics of C. freundii have become a significant source of diarrheal infections and food poisoning among immune-compromised patients and newborns. Impulsive usage of antibiotics and these adaptive virulence characteristics has modulated the C. freundii into multidrug-resistant (MDR) bacteria. Conventional approaches are futile against MDR C. freundii. Materials and Methods: The current study exploits the modern computational-based vaccine design approach to treat infections related to MDR C. freundii. A whole proteome of C. freundii (strain: CWH001) was retrieved to screen pathogenic and nonhomologous proteins. Six proteins were shortlisted for the selection of putative epitopes for vaccine construct. Highly antigenic, nonallergen, and nontoxic eleven B-cell, HTL, and TCL epitopes were selected for mRNA- and peptide-based multi-epitope vaccine construct. Secondary and tertiary structures of the multi-epitope vaccine (MEVC) were designed, refined, and validated. Results: Evaluation of population coverage of MHC-I and MHC-II alleles were 72% and 90%, respectively. Docking MEVC with TLR-3 receptor with the binding affinity of 21.46 (kcal/mol) occurred through the mmGBSA process. Further validations include codon optimization with an enhanced CAI value of 0.95 and GC content of about 51%. Immune stimulation and molecular dynamic simulation ensure the antibody production upon antigen interaction with the host and stability of the MEVC construct, respectively. Conclusions: These interpretations propose a new strategy to combat MDR C. freundii. Further, in vivo and in vitro trials of this vaccine will be valuable in combating MDR pathogens.

Indexed as

Citrobacter freundiiProteomicsAnti-Bacterial AgentsEpitopesHumansInfant, NewbornPeptidesProteomeRNA, MessengerToll-Like Receptor 3Vaccines, SubunitAnti-Bacterial AgentsEpitopesPeptidesProteomeRNA, MessengerToll-Like Receptor 3Vaccines, SubunitAMRantibiotic resistancebioinformaticsglobal hazardshealth issues

Identifiers

PMID36295517
PMCPMC9610710
OpenAlexW4297542704

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.