Evidence map›Paper›PMID 41888742›Full record

ArticleBMC infectious diseases2026

Investigation of mRNA expressions in nasopharyngeal and oropharyngeal swab samples in active SARS-CoV-2 infection and after SARS-CoV-2 infection.

Burcu Çaykara Peran, Güler Öztürk, Sadrettin Pençe, Nurettin Yiyit, Burhanettin Yalçınkaya

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Article in BMC infectious diseases, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Burcu Çaykara PeranDepartment of Physiology, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye. burcu.caykaraperan@sbu.edu.tr.
Güler ÖztürkDepartment of Physiology, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Sadrettin PençeDepartment of Physiology, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Türkiye.
Nurettin YiyitYedikule Chest Diseases and Surgery Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye.
Burhanettin YalçınkayaTUBITAK National Metrology Institute (TUBITAK UME), Kocaeli, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSARS-CoV-2 enters host cells primarily through angiotensin-converting enzyme 2 (ACE2) and requires proteolytic activation by transmembrane serine protease 2 (TMPRSS2) or cysteine proteases cathepsin B and L (CTSB/L). The expression levels of these host factors may influence viral entry, tissue tropism, and disease severity. This study aimed to investigate differences in ACE2, TMPRSS2, CTSB, and CTSL gene expression in nasopharyngeal and oropharyngeal swab samples obtained from individuals during active SARS-CoV-2 infection and in the post-infection period. MATERIALS AND

methodsNasopharyngeal and oropharyngeal swab samples (active infection: n = 24; post-infection: n = 24) were collected and placed in viral transport medium. After RNA isolation was performed, complementary DNA synthesis was carried out with FIREScript RT cDNA Synthesis Mix with Oligo (dT), and gene expression was quantified using 5× HOT FIREPol EvaGreen qPCR Mix Plus (no ROX) (Solis BioDyne®). Relative expression levels were determined using the 2−ΔΔCT method.

resultsACE2 expression was 4.2-fold higher in the active infection group than in the post-infection group (p < 0.05), whereas TMPRSS2, CTSB, and CTSL expression did not differ significantly between groups (p > 0.05). Within the active infection group, CTSB expression was 10.4-fold higher in nasopharyngeal swabs compared to oropharyngeal swabs (p = 0.035). TMPRSS2 expression showed a non-significant trend toward a 3-fold reduction in nasopharyngeal samples (p = 0.051). In the post-infection group, CTSB expression was approximately 2-fold higher and CTSL expression 3-fold lower in nasopharyngeal versus oropharyngeal samples (p > 0.05). Notably, TMPRSS2 expression was significantly reduced (~ 7-fold) in nasopharyngeal compared to oropharyngeal swabs (p = 0.041).

conclusionsOur findings demonstrate that ACE2, TMPRSS2, CTSB, and CTSL exhibit dynamic and site-specific expression patterns during and after SARS-CoV-2 infection. The elevated ACE2 expression in active infection and differential regulation of proteases between nasopharyngeal and oropharyngeal sites suggest distinct host–virus interactions depending on anatomical localization.

Indexed as

COVID-19NasopharynxOropharynxRNA, MessengerAdultAngiotensin-Converting Enzyme 2Cathepsin BCathepsin LFemaleHumansMaleMiddle AgedPeptidyl-Dipeptidase ASARS-CoV-2Serine EndopeptidasesACE2 protein, humanAngiotensin-Converting Enzyme 2Cathepsin BCathepsin LCTSB protein, humanCTSL protein, humanPeptidyl-Dipeptidase ARNA, MessengerSerine EndopeptidasesTMPRSS2 protein, humanACE2CTSBCTSLSARS-CoV-2TMPRSS2

Identifiers

PMID41888742
PMCPMC13188349

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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.