Differentially expressed plasmatic microRNAs in Brazilian patients with Coronavirus disease 2019 (COVID-19): preliminary results

被引:19
作者
Nicoletti, Aline de Souza [1 ]
Visacri, Marilia Berlofa [1 ]
da Silva Correa da Ronda, Carla Regina [2 ]
do Nascimento Silva Vasconcelos, Pedro Eduardo [1 ]
Franca Quintanilha, Julia Coelho [3 ]
de Souza, Rafael Nogueira [1 ]
Ventura, Deise de Souza [4 ]
Eguti, Adriana [4 ]
de Souza Silva, Lilian Ferreira [4 ]
Perroud Junior, Mauricio Wesley [1 ,4 ]
Catharino, Rodrigo Ramos [2 ,5 ]
Reis, Leonardo Oliveira [6 ]
dos Santos, Luiz Augusto [7 ]
Duran, Nelson [8 ]
Favaro, Wagner Jose [8 ]
Lancellotti, Marcelo [2 ]
da Costa, Jose Luiz [2 ]
Moriel, Patricia [2 ]
Pincinato, Eder de Carvalho [1 ]
机构
[1] Univ Estadual Campinas, Sch Med Sci, Campinas, SP, Brazil
[2] Univ Estadual Campinas, Fac Pharmaceut Sci, Candido Portinari St 200, BR-13083871 Campinas, SP, Brazil
[3] Univ North Carolina Chapel Hill, UNC Eshelman Sch Pharm, Chapel Hill, NC USA
[4] Hosp Estadual Sumare Dr Leandro Francheschini, Sumare, SP, Brazil
[5] Univ Estadual Campinas, Innovare Biomarkers Lab, Campinas, SP, Brazil
[6] Univ Estadual Campinas, UroSci Lab, Campinas, SP, Brazil
[7] Hosp Municipal Paulinia, Paulinia, SP, Brazil
[8] Univ Estadual Campinas, Lab Urogenital Carcinogenesis & Immunotherapy, Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
COVID-19; SARS-CoV-2; Biomarkers; Epigenomics; microRNAs;
D O I
10.1007/s11033-022-07338-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background Coronavirus disease 2019 (COVID-19) is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is known that host microRNAs (miRNAs) can be modulated to favor viral infection or to protect the host. Herein, we report preliminary results of a study aiming at identifying differentially expressed plasmatic miRNAs in Brazilian patients with COVID-19. Methods and results miRNAs were extracted from the plasma of eight patients with COVID-19 (four patients with mild COVID-19 and four patients with severe/critical COVID-19) and four healthy controls. Patients and controls were matched for sex and age. miRNA expression levels were detected using high-throughput sequencing. Differential miRNA expression and enrichment analyses were further evaluated. A total of 18 miRNAs were differentially expressed between patients with COVID-19 and controls. miR-4433b-5p, miR-6780b-3p, miR-6883-3p, miR-320b, miR-7111-3p, miR-4755-3p, miR-320c, and miR-6511a-3p were the most important miRNAs significantly involved in the PI3K/AKT, Wnt/beta-catenin, and STAT3 signaling pathways. Moreover, 42 miRNAs were differentially expressed between severe/critical and mild patients with COVID-19. miR-451a, miR-101-3p, miR-185-5p, miR-30d-5p, miR-25-3p, miR-342-3p, miR-30e-5p, miR-150-5p, miR-15b-5p, and miR-29c-3p were the most important miRNAs significantly involved in the Wnt/beta-catenin, NF-kappa beta, and STAT3 signaling pathways. Conclusions If validated by quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) in a larger number of participants, the miRNAs identified in this study might be used as possible biomarkers for the diagnosis and severity of COVID-19.
引用
收藏
页码:6931 / 6943
页数:13
相关论文
共 44 条
[1]   Micro-RNAs in the regulation of immune response against SARS CoV-2 and other viral infections [J].
Abu-Izneid, Tareq ;
AlHajri, Noora ;
Ibrahim, Abdallah Mohammad ;
Javed, Md. Noushad ;
Salem, Khairi Mustafa ;
Pottoo, Faheem Hyder ;
Kamal, Mohammad Amjad .
JOURNAL OF ADVANCED RESEARCH, 2021, 30 :133-145
[2]   Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19 [J].
Ackermann, Maximilian ;
Verleden, Stijn E. ;
Kuehnel, Mark ;
Haverich, Axel ;
Welte, Tobias ;
Laenger, Florian ;
Vanstapel, Arno ;
Werlein, Christopher ;
Stark, Helge ;
Tzankov, Alexandar ;
Li, William W. ;
Li, Vincent W. ;
Mentzer, Steven J. ;
Jonigk, Danny .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (02) :120-128
[3]   'The Double-Edged Sword' - An hypothesis for Covid-19-induced salivary biomarkers [J].
Adeoye, John ;
Thomson, Peter .
MEDICAL HYPOTHESES, 2020, 143
[4]   Predicting effective microRNA target sites in mammalian mRNAs [J].
Agarwal, Vikram ;
Bell, George W. ;
Nam, Jin-Wu ;
Bartel, David P. .
ELIFE, 2015, 4
[5]   MicroRNA Involvement in Signaling Pathways During Viral Infection [J].
Barbu, Madalina Gabriela ;
Condrat, Carmen Elena ;
Thompson, Dana Claudia ;
Bugnar, Oana Larisa ;
Cretoiu, Dragos ;
Toader, Oana Daniela ;
Suciu, Nicolae ;
Voinea, Silviu Cristian .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2020, 8
[6]   COVID-19: a meta-analysis of diagnostic test accuracy of commercial assays registered in Brazil [J].
Castro, Rodolfo ;
Luz, Paula M. ;
Wakimoto, Mayumi D. ;
Veloso, Valdilea G. ;
Grinsztejn, Beatriz ;
Perazzo, Hugo .
BRAZILIAN JOURNAL OF INFECTIOUS DISEASES, 2020, 24 (02) :180-187
[7]   Blood molecular markers associated with COVID-19 immunopathology and multi-organ damage [J].
Chen, Yan-Mei ;
Zheng, Yuanting ;
Yu, Ying ;
Wang, Yunzhi ;
Huang, Qingxia ;
Qian, Feng ;
Sun, Lei ;
Song, Zhi-Gang ;
Chen, Ziyin ;
Feng, Jinwen ;
An, Yanpeng ;
Yang, Jingcheng ;
Su, Zhenqiang ;
Sun, Shanyue ;
Dai, Fahui ;
Chen, Qinsheng ;
Lu, Qinwei ;
Li, Pengcheng ;
Ling, Yun ;
Yang, Zhong ;
Tang, Huiru ;
Shi, Leming ;
Jin, Li ;
Holmes, Edward C. ;
Ding, Chen ;
Zhu, Tong-Yu ;
Zhang, Yong-Zhen .
EMBO JOURNAL, 2020, 39 (24)
[8]   Prediction and Analysis of SARS-CoV-2-Targeting MicroRNA in Human Lung Epithelium [J].
Chow, Jonathan Tak-Sum ;
Salmena, Leonardo .
GENES, 2020, 11 (09) :1-12
[9]   COVID-19 vaccines: The status and perspectives in delivery points of view [J].
Chung, Jee Young ;
Thone, Melissa N. ;
Kwon, Young Jik .
ADVANCED DRUG DELIVERY REVIEWS, 2021, 170 (170) :1-25
[10]   The cytokine storm in COVID-19: An overview of the involvement of the chemokine/chemokine-receptor system [J].
Coperchini, Francesca ;
Chiovato, Luca ;
Croce, Laura ;
Magri, Flavia ;
Rotondi, Mario .
CYTOKINE & GROWTH FACTOR REVIEWS, 2020, 53 :25-32