key: cord-0805020-vo87ug59 authors: Torabi, Raheleh; Ranjbar, Reza; Halaji, Mehrdad; Heiat, Mohammad title: Aptamers, the bivalent agents as probes and therapies for coronavirus infections: A systematic review date: 2020-07-04 journal: Mol Cell Probes DOI: 10.1016/j.mcp.2020.101636 sha: 498cc5fd1b1fe1a659e8b60c0d93024ea8bb7ca7 doc_id: 805020 cord_uid: vo87ug59 The recently known coronavirus, SARS-CoV-2, has turn into the greatest global health challenge, affecting a large number of societies. The lack of specific treatment and gold-standard diagnostic system has made the situation more complicated. Efforts have led to production of several diagnostic kits that are associated with limitations such as inadequate sensitivity and accuracy. Aptamers as multipotent biological probes could be promising candidates to design sensitive and specific biosensors. Although few studies have introduced specific aptamer types of coronavirus, they may help us select the best approach to obtain specific aptamers for this virus. On the other hand, some of already-introduced aptamers have shown the inhibitory effects on coronavirus that could be applied as therapeutics. The present study has provided a systematic overview on use of aptamer-based biosensors and drugs to diagnose and treat coronavirus. Coronaviruses (CoVs) are respiratory viruses that can cause infections (e.g. common cold and pneumonia) in mammals and birds. There are six types of CoVs (HCoVs) that may affect the humans: HCoV-229E, HCoV-OC43, HCoV-NL63, HCoV-HKU1, SARS-CoV and MERS-CoV. The causes of two major outbreaks in the first two decades of the contemporary century belong to the beta CoVs including Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) that was an epidemic in 2002 to 2003, and the Middle East Respiratory Syndrome Coronavirus (MERS-CoV), that has been epidemic since 2012. The latest onslaught of beta CoVs subfamily has been conducted by SARS-CoV-2 since December 12, 2019. COVID-19, the disease of this fighter virus, is now a vigorous threat to global health security [1] . World Health Organization (WHO) is concerned about the global public health and high-risk health systems since there are currently no specific vaccines or drugs to prevent or treat COVID-19 [2] . However, many efforts are being made to tackle this spiked virus. The important bottlenecks for the management of COVID-19 are diagnostics and therapeutics. The common diagnostic test for COVID-19 is real-time reverse transcription polymerase chain reaction (RT-PCR) [3] . Regarding some reports the one-step rRT-PCR assays based on specific TaqMan probes have had a detection limit as few as 4 to 10 copies of RNA template per reaction [4] [5] . However most of these tests show low sensitivity and specificity, so they do not work well enough to be routinely used. Thus, it is critical to invent new potent diagnostic tools. The other traditional laboratory-based assays like virus culture, enzyme-linked immunosorbent assay (ELISA), western blotting, and serological antibody detection methods require virus isolation or DNA/RNA extraction that make them time-consuming and increasing the probability of virus spreading. These techniques also require expensive laboratory equipment and expert operators. These constrictions raise the response time and expenses which impact the quality of patient care [6] . Unlike the common laboratory assays, biosensors can produce quantitative signals proportional to the analyte concentration by the interaction of chemical or biological receptors with targets. Antibodies are applied as detector elements in the most viral biosensors. However, nucleic acids are recently recruited as the receptors which transduce signals to detect targets. DNA biosensors could detect a great variety of molecules with high affinity and specificity [7] . Aptamer, one of the novel DNA receptors, is a single-stranded folded RNA or ssDNA that can bind and detect various nucleic and non-nucleic acid molecules with high affinity and specificity. The application of aptamer probes for virus detection has increased in recent years. Aptamers could detect any viral infection markers, including viral genes, proteins, and antibodies. By applying some approaches, aptasensors can discriminate infected host cells from uninfected ones or active from inactive viral forms [8] . The highly mutated characteristic of viral genomes can lead to variability, and escaping from the host immune response makes most of drugs inefficient. Aptamers are novel potent candidates, which can treat viral infections by modulating the immune response, inhibiting the viruses penetrating the cells, or disrupting the replication enzymes. Furthermore, a variety types of modifiers, drugs and dyes could easily conjugate the aptamers without altering their primary properties to increase their in vivo stability and bioactivity [8] . Despite the eligibility and the effects of aptamer as a diagnostic candidate for COVID-19, as well as their considerable advantages over similar molecules such as siRNA and monoclonal antibodies [8] , there are some challenges toward the widespread use of aptamers for therapeutic purposes. The first challenge is the renal clearance which limits the circulation time of aptamers due to its low molecular weight that could be solved by conjugating with high weigh molecules. Also, the toxicological information regarding aptamers in humans is very limited. However aptamers have several advantages over antibodies, such as higher stability, simple synthesis, and modification. Among the isolated aptamers, Pegaptanib (Macugen) is the only aptameric drug used for the treatment of neovascular (wet) age-related macular degeneration (AMD) that has been able to gain clinical and marketing approvals. Therefore, it is critical to continue the studies to find applicable therapeutic antiviral aptamers [9] . The present systematic review aimed to describe diagnostic and therapeutic approaches found by aptamer as a versatile tool for rapid diagnostics and therapeutics for coronaviruses. All stages of this review followed the published protocol by Liberati et al [10] . The metaanalysis protocol was not applied due to the very limited available evidence on the topic and due to the urgency of the matter. In this review, these designs were considered for inclusion. Introduction of DNA and RNA aptamers for coronavirus • Application of DNA and RNA aptamers for the diagnosis or therapy of coronavirus No publication date, language, or publication status restrictions were imposed. Studies were identified by searching through electronic databases and scanning the reference lists of articles. The sources of the literature review encompassed Scopus, Pubmed, and Google scholars. The last search was run on June 21, 2020. The following terms were used to search all the trials, registers, and databases: SARS AND We included the entire original and review articles that had been designed or applied aptamers for coronaviruses. Then, in an unblended and standardized manner, we evaluated the eligibility of the articles by looking at the titles, abstracts, and full-text reports to determine inclusion and exclusion decisions and extract data from all eligible studies. To ascertain the validity of studies, pairs of reviewers worked independently and with adequate reliability determined the validity, efficiency, and application of aptamers. Finally, we used the MFold program to predict secondary structures of coronaviruses aptamers based on the Zuker algorithm [11] . After searching in Scopus, Pubmed, and Google scholar databases, a total of 41 studies involving aptamer and coronavirus were identified in this review. Then, after adjusting for duplicates and discarding articles that did not meet the criteria, three main articles on diagnostic aptamers against coronaviruses and two other studies on therapeutic aptamers remained. No reprinted relevant studies were obtained ( Figure 1 ). As we explored, there were only three published original research articles about diagnostic aptamers for coronaviruses (Table 1) . SARS-CoV nucleocapsid (N) protein forms a helical core in the viral envelope that plays a critical role during the viral life cycle. It can improve the efficiency of subgenomic viral RNA transcription [12] . According to the studies, N protein can be tracked in serum for the early detection of SARS-CoV [13] . Ahn et al. used a SELEX procedure to isolate two RNA aptamers (aptamer-1 and aptamer-2) binding specifically to the C-terminal region of SARS-CoV N protein with low dissociation constants (0.81 nM, and 3.35 nM, respectively). The result showed that aptamer-1 binds to N protein with a higher affinity than aptamer-2. They also applied SPR to confirm this result which appeared to be better than the antibody against N protein (KD = 1.65 nM for aptamer-1 vs KD = 2.1 µM for antibody). To fabricate a detection system for N protein, Ahn et al. used a streptavidin-coated 96-well plate for immobilization of aptamer. After incubating N protein, a polyclonal antibody was applied to the captured agent and then a labeled monoclonal antibody to signal production. The detection limit of this method was 20 pg/ml (420 fM) of N protein [14] which was similar to that of ELISA with polyclonal and monoclonal antibodies [15] . Moreover, they used a polyclonal antibody and the FITC-conjugated secondary antibody to establish a nanoarray chip assay with a detection limit of 42 fM which was ten times more sensitive than previous chemiluminescence assay [14] . In the second study, Cho et al., isolated a single-stranded DNA (ssDNA) aptamer with specific binding to N protein of SARS-CoV with a high affinity (Kd = 4.93±0.30 nM). They applied the selected aptamer in western blot analysis, showing that this aptamer could be a worthy recognizer element instead of the monoclonal antibodies [16] . Since, SARS-CoV N protein is more than 90% homologous with protein sequence of SARS-CoV-2, a research group decided to investigate the affinity of the previously reported SARS-CoV N protein aptamers by Cho et al. [16] and modified variants against SARS-CoV-2 N protein by Enzyme-Linked Aptamer Binding Assay (ELAA). They immobilized SARS-CoV-2 N protein into the 96-well-plate and then added 5-biotinylated aptamers. Subsequently, the avidin-HRP was applied to recognize the biotin signal by measuring the absorbance using tetramethylbenzidine as substrate. Their results showed that all aptamers could specifically bind to SARS-CoV-2 N protein [17] . It has been identified that SARSCoV-2 infects the human respiratory epithelial cells via ( Figure 2 ). Despite of all efforts, scientists have not yet discovered the first line drug against COVID-19. NTPase/Helicase could be considered as a potent target to develop agents against SARS-CoV [20, 21] . These drugs can bind to the helicase and inhibit its activity through blocking the binding to nucleic acids [22] . Nonstructural Protein 10 (nsP10) is an enzyme with NTPase/Helicase activity which can threaten the life of SARS-CoV as its Achilles heel. In this line, we found two published original research articles about the therapeutic aptamers against coronaviruses ( Table 2 ). In the first research, Shum et al. isolated two different DNA aptamers in structure, G-quadruplex, and non-G-quadruplex, via Ni-NTA magnetic beads SELEX. Both of these aptamers had a positive effect on ATPase activity with low Km values. However, only the non-G-quadruplex one inhibits the SARS-CoV helicase activity to unwind nucleic acids. The aptamers could bind to the binding sites of helicase and change their conformation [23] . The MFold program was applied to predict the secondary structures of these DNA aptamers [11] (Figure 3 ). In the second research, Jang et al., presented specific RNA aptamers against nsP10. They used the conventional SELEX to find RNA aptamers against NTPase/Helicase in SARS-CoV from an RNA library, which resulted in an enriched RNA aptamer pool (ES15 RNA). This aptameric pool could decrease the unwinding of nucleic acid and ATPase activity of the helicase (IC50 =1.2 nM) [24] . They pointed out that the inhibitory effect of these RNA aptamers was derived from AG-rich conserved sequence which could be considered as anti-SARS-CoV agents ( Figure 3 ). Currently, the major approaches to detect SARS-CoV-2 are nucleic acid amplification-based diagnostic methods. These methods show high sensitivity and specificity to detect nucleic acid targets. They could easily differentiate among strains and species with no need for viable organism. These methods can be set up easily and get high level approval for clinical diagnostic applications [25] . However, using these methods can cause some limitations and technical problems [26] . Apart from being high cost, the major problem is that these methods may have a large number of false positive and negative results caused by low RNA stability, DNA/RNA contaminants, and the presence of enzymes inhibitors in biological samples [27, 28] . Also, these methods may detect both active and inactive viruses that could lead to false positive results. Thus, the results could not certainly differentiate between patients, vectors, recovered individuals and samples. Accordingly, a challenge has arisen among scientists since recovered people from COVID-19, continue to test positive without showing symptoms that interfere with medical decision making [29] [30] [31] . The efficiency of RT-PCR, which is now the standard diagnosis methods for SARS-CoV-2, relies on the adequate viral RNA (viral load) and it changes significantly between patients and even, during the course of the infection within a single individual [32] . These constraints have justified applying other efficient techniques such as aptamer-based platforms. Some of the advantages and disadvantages of these two competitors are summarized in Table 3 . In this study, we intended to implement a comprehensive systematic review study on all isolated aptamer molecules against coronaviruses. However, we did not use the meta-analysis protocol due to the very limited available evidence on the topic and the urgency of the matter. Few high-affinity and specific aptamers have been reported for diagnosis and treatment of coronaviruses; however, only one study has reported the isolation of aptamer against SARS-CoV-2 [18] . Due to structural similarities among coronaviruses, it may possible to fabricate the aptamer-based detection systems or aptamer-based drugs for SARS-CoV-2 according to previously isolated aptamers for other coronaviruses. As one of the main coronavirus proteins, the SARS-CoV N protein, has a great similarity with that in SARS-CoV-2 [33] . An N protein specific RNA aptamer was isolated and applied in aptamer-antibody hybrid immunoassays with a very low detection limit (2 pg/ml of N protein) by Ahn et al. [14] . Cho et al., also reported another type of aptamer (ssDNA aptamer), which showed high affinity compatible with western blot analysis [16] . It could be assumed that these two reported specific aptamers of SARS-CoV N protein could provide a platform to detect N protein of SARS-CoV-2 through evaluation by experimental analysis, SELEX modeling and molecular dynamic simulation [34] . Some modifications in sequence and structure of aptamers may produce specific aptamer for SARS-CoV-2 N protein. Accordingly combination of therapeutic aptamers with other novel technologies such as nanobiotechnolgy [38] . COVID-19 is a dangerous threat to public health, global disciples, and economics. The first step to treat this viral disease is a rapid and accurate diagnosis that can prevent its contagion. Recently, Nucleic acid aptamers have been confirmed to be useful as medications and diagnostic probes [39] . According to the previous studies and from a general point of view, it seems that the aptamer molecules could be effective anti-coronavirus agents in both diagnosis and treatment. Although no aptamers have been isolated for SARS-Cov-2 until now, it seems that modeling of other coronavirus aptamers can be helpful to find an appropriate shortcut to achieve the best targets and subsequently the best antidote or diagnostic assays. The Helicase enzyme has an important role in viral replication and proliferation. Therefore, it could be considered as a potent target to develop the coronavirus therapeutic aptamers [23, 24] . N protein could be also a potent target to detect and inhibit COVID-19 due to its crucial role in the synthesis of viral RNA and SARS detection. By applying aptamers as sensitive diagnostic elements, we will be able to fabricate rapid, sensitive, low-cost, and user-friendly diagnostic tools of small volume clinical samples. 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