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

被引:18
|
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
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