Evidence map›Paper›PMID 35905113›Full record

ArticlePloS one2022

Analysis of multi-strain infection of vaccinated and recovered population through epidemic model: Application to COVID-19.

Olusegun Michael Otunuga

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

1 author.

Olusegun Michael OtunugaDepartment of Mathematics, Augusta University, Augusta, GA, United States of America.ORCID 0000-0002-8360-9094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work, an innovative multi-strain SV EAIR epidemic model is developed for the study of the spread of a multi-strain infectious disease in a population infected by mutations of the disease. The population is assumed to be completely susceptible to n different variants of the disease, and those who are vaccinated and recovered from a specific strain k (k ≤ n) are immune to previous and present strains j = 1, 2, ⋯, k, but can still be infected by newer emerging strains j = k + 1, k + 2, ⋯, n. The model is designed to simulate the emergence and dissemination of viral strains. All the equilibrium points of the system are calculated and the conditions for existence and global stability of these points are investigated and used to answer the question as to whether it is possible for the population to have an endemic with more than one strain. An interesting result that shows that a strain with a reproduction number greater than one can still die out on the long run if a newer emerging strain has a greater reproduction number is verified numerically. The effect of vaccines on the population is also analyzed and a bound for the herd immunity threshold is calculated. The validity of the work done is verified through numerical simulations by applying the proposed model and strategy to analyze the multi-strains of the COVID-19 virus, in particular, the Delta and the Omicron variants, in the United State.

Indexed as

COVID-19EpidemicsBasic Reproduction NumberHumansSARS-CoV-2

Identifiers

PMID35905113
PMCPMC9337708

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.