Evidence map›Paper›PMID 40225260›Full record

ArticleIranian journal of public health2025

Phylogenetic and Mutational Analysis of the Tax Gene in the Human T-Lymphotropic Virus 1-Associated HAM/TSP in Comparison with Asymptomatic Careers.

Farzad Babakhani, Atefeh Bahavar, Soosan Zare, Mohammad Ali Sahraian, Abbas Rahimi Foroushani, Seyed Mohammad Jazayeri, Mahdi Mohammaditabar, Ghazaleh Molaverdi, Sayed-Hamidreza Mozhgani, Mehdi Norouzi

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Article in Iranian journal of public health, 2025. 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

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Epidemiology and Clinical Outcomes of HTLV-1: A Comprehensive Narrative Review of Endemic and Nonendemic Regions.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2026
    Review
  4. Phylogenetic and Mutational Analysis of theIranian journal of public health · 2025
    Article
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Farzad BabakhaniDepartment of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Atefeh BahavarDepartment of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Soosan ZareSina Hospital, University of Tehran, Tehran, Iran.
Mohammad Ali SahraianMS Research Centre, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Abbas Rahimi ForoushaniDepartment of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Seyed Mohammad JazayeriNon-Communicable Diseases Research Center, Alborz University of Medical Sciences, Karaj, Iran.
Mahdi MohammaditabarStudent Research Committee, Alborz University of Medical Sciences, Karaj, Iran.
Ghazaleh MolaverdiStudent Research Committee, Alborz University of Medical Sciences, Karaj, Iran.
Sayed-Hamidreza MozhganiDepartment of Microbiology, School of Medicine, Alborz University of Medical Sciences, Karaj, Iran.
Mehdi NorouziResearch Center for Clinical Virology, Tehran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Human T-lymphotropic virus 1 (HTLV-1) is a member of the Retroviridae family that can cause two groups of diseases: HTLV-1-associated myelopathy/tropical spastic paraparesis (HAM/TSP) and adult T-cell leukemia/lymphoma (ATLL). Despite HTLV having seven different subtypes, cosmopolitan subtype A is responsible for most HTLV-1-related disorders and is the most widely dispersed type globally, including in the Middle East, known to be an endemic area for the virus. Therefore, due to the importance of determining the subtypes of this virus, we aimed to explore the subtypes of HTLV-1 in Iran. Methods: In this cross-sectional study, we screened 140 Blood samples for HAM/TSP infection and approximately 4,500 samples for asymptomatic carriers (ACs) from Sina Hospital, Iran between 2020 and 2021. Positive samples were used for phylogenetic and mutational analysis to compare ACs and HAM/TSP cases via the Tax segment of HTLV. To identify the genotype of positive samples, the Maximum Likelihood method was used to construct the phylogenetic tree based on the positive samples. Results: All Iranian isolates were clustered as HTLV-1a subgroups. Moreover, all of our samples have undergone positive selection pressure. Furthermore, we detected unique mutations in Iranian HAM/TSP and ACs sequences. Conclusion: All of the Iranian Tax proteins are under positive selection pressure with respect to Japanese isolates. Interestingly, we detect specific mutation patterns in the sequences. Positions 51, 82, 109, 172, 232, and 339 in the aa sequence have undergone mutations specific to Iranian HTLV-1; and in positions 22 and 146 aa we detected mutations unique to ACs and HAM/TSP, respectively.

Indexed as

Human T-lymphotropic virus 1 (HTLV-1)Mutational analysisPhylogenetic analysis

Identifiers

PMID40225260
PMCPMC11992914

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