Expression analysis of DDC, dACE2, and EPO genes in Moroccan COVID-19 patients: links to viral load and demographics

Authors

  • Oumaima Laazaazia Virology Unit, Viral Hepatitis Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco
  • Ahd Ouladlahsen Service des Maladies Infectieuses, CHU Ibn Rochd, Casablanca, Morocco https://orcid.org/0000-0003-4298-4610
  • Safaa Aqillouch Virology Unit, Viral Hepatitis Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco https://orcid.org/0009-0005-2439-220X
  • Haya Altawalah Department of Microbiology, Faculty of Medicine, Kuwait University, Kuwait
  • Rachid Noureddine Virology Unit, Viral Hepatitis Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco
  • M’hammed Sarih Service de Parasitologie et des Maladies Vectorielles, Institut Pasteur du Maroc, Casablanca, Morocco https://orcid.org/0000-0002-4375-0077
  • Pascal Pineau Institut Pasteur, Université Paris Cité, Unité “Organisation Nucléaire et Oncogenèse”, INSERM U993, Paris, France https://orcid.org/0000-0002-9407-1592
  • Abderrahmane Maaroufi Virology Unit, Viral Hepatitis Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco
  • Mustapha Lkhider Laboratory of Virology, Microbiology, Quality and Biotechnology/Ecotoxicology and Biodiversity, Hassan II University, Faculté des Sciences et Techniques, Mohammedia, Morocco https://orcid.org/0000-0002-4886-601X
  • Sayeh Ezzikouri Virology Unit, Viral Hepatitis Laboratory, Institut Pasteur du Maroc, Casablanca, Morocco https://orcid.org/0000-0002-3982-6163

DOI:

https://doi.org/10.3855/jidc.21079

Keywords:

COVID-19, SARS-CoV-2, DDC, dACE2, EPO

Abstract

Introduction: Interactions between host and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are incompletely understood. Studies have highlighted the roles of L-dopa decarboxylase (DDC), interferon-inducible truncated isoform of angiotensin-converting enzyme 2 (dACE2), and immunomodulatory hypoxia-regulated gene erythropoietin (EPO) in viral infections. This study investigated the expression levels of DDC, dACE2, and EPO in 136 coronavirus disease 2019 (COVID-19) patients and 88 controls.

Methodology: Real-time quantitative reverse transcription polymerase chain reaction (RT-qPCR) was used to quantify mRNA levels of DDC, dACE2, and EPO; and the SARS-CoV-2 viral load in nasopharyngeal swabs.

Results: Significantly elevated levels of dACE2 (p = 0.003), DDC (p = 0.004), and EPO (p = 0.006) were observed in patients compared to controls. No correlation with the viral load (DDC: r = 0.12, p = 0.136; EPO: r = 0.02, p = 0.802; dACE2: r = 0.05, p = 0.491), and no associations with age or gender (all p > 0.05) were noted. There were positive correlations between DDC and dACE2 mRNA levels in infected (r = 0.31, p = 0.0002) and uninfected individuals (r = 0.25, p = 0.015); and between DDC and EPO in infected (r = 0.22, p = 0.008) and uninfected individuals (r = 0.27, p = 0.010). There was a positive correlation between dACE2 and EPO mRNA levels in both groups (infected: r = 0.22, p = 0.007; uninfected: r = 0.38, p = 0.0002).

Conclusions: DDC, dACE2, and EPO may contribute to COVID-19 pathogenesis through mechanisms independent of viral load, age, or gender.

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Published

2025-09-30

How to Cite

1.
Laazaazia O, Ouladlahsen A, Aqillouch S, Altawalah H, Noureddine R, Sarih M, Pineau P, Maaroufi A, Lkhider M, Ezzikouri S (2025) Expression analysis of DDC, dACE2, and EPO genes in Moroccan COVID-19 patients: links to viral load and demographics. J Infect Dev Ctries 19:1299–1307. doi: 10.3855/jidc.21079

Issue

Section

Coronavirus Pandemic