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ArticleMolecular biology reports2025

Comparative viral load analysis of torque Teno virus and Torque teno mini virus in COVID-19 infected and non-infected individuals in the United Arab Emirates.

Gayathri Arumughan Kanu, Raed Abu Odeh, Zamberi Sekawi, Zulkefley Othman

Abstract readComparative Study
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Article in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Gayathri Arumughan KanuFaculty of Medicine and Health Sciences, Department of Biomedical Sciences, Universiti Putra Malaysia, Serdang, Malaysia.ORCID http://orcid.org/0000-0001-7825-245X
Raed Abu OdehDepartment of Medical Laboratory Sciences, College of Health Sciences, University of Sharjah, Sharjah, United Arab Emirates.ORCID http://orcid.org/0000-0001-9123-6956
Zamberi SekawiFaculty of Medicine and Health Sciences, Department of Biomedical Sciences, Universiti Putra Malaysia, Serdang, Malaysia.ORCID http://orcid.org/0000-0002-5387-9640
Zulkefley OthmanFaculty of Medicine and Health Sciences, Department of Biomedical Sciences, Universiti Putra Malaysia, Serdang, Malaysia. zulkefley_os@upm.edu.my.ORCID http://orcid.org/0000-0001-6973-0747

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTorque teno virus (TTV) and Torque teno mini virus (TTMV) are highly prevalent, non-pathogenic viruses from the Anelloviridae family that commonly circulate in healthy individuals. Their replication dynamics are closely linked to the host immune status, with viral loads typically increasing during immune suppression or dysregulation associated with viral infections, transplantation, or chronic inflammation. Emerging evidence suggests that TTV may serve as a biomarker of immune competence, with increasing interest in its role during SARS-CoV-2 infection. This study investigated the presence of TTV and TTMV among the study samples, viral load (VL), and demographic associations of TTV and TTMV in COVID-19 infected and non-infected individuals in the United Arab Emirates (UAE).

methodsWe analysed 278 plasma samples, 139 COVID-19 infected samples and 139 non-infected samples, via species-specific nested PCR targeting conserved genomic regions downstream of the TATA box in the range of nucleotide positions 99–227 for TTV and 178–303 for TTMV. In-house clones constructed from non-infected COVID-19 samples served as positive controls for the detection and quantification of TTV and TTMV. Real-time qPCR was used to quantify the viral loads. Furthermore, demographic data, including age, BMI, and COVID-19 symptoms, were gathered, and statistically analysed.

resultsThe TTV-VL was significantly higher in COVID-19 infected individuals (p < 0.001), whereas the TTMV-VL was not significantly different between the groups (p = 0.948). No statistically significant correlation was found between TTV-VL and age or BMI in individual groups, although age-based subgroup analysis revealed notable differences in the co-infected study samples. In co-infected individuals (those harbouring both TTV and TTMV), TTV-VL remained significantly elevated in the COVID-19 infected groups, whereas TTMV-VL remained non-significant.

conclusionOur findings demonstrate that TTV-VL is elevated in association with COVID-19 infection, suggesting its potential as a marker of immune modulation during SARS-CoV-2 infection. In contrast, TTMV-VL appears to be unaffected by COVID-19 status, indicating different replication dynamics between these related viruses during immune challenge. This study advances our knowledge of the clinical relevance of TTV as a biomarker of immune function and offers the first thorough analysis of anelloviruses viral loads in UAE study samples in the context of COVID-19.

Indexed as

COVID-19DNA Virus InfectionsTorque teno virusViral LoadAdultFemaleHumansMaleMiddle AgedSARS-CoV-2United Arab EmiratesCOVID-19Demographic analysisTTMVTTVUAEViral cloningViral load

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