| Literature DB >> 34664166 |
Rokeya Akter1, Md Habibur Rahman2, Tanima Bhattacharya3, Deepak Kaushik4, Vineet Mittal5, Jatin Parashar5, Kuldeep Kumar6, Md Tanvir Kabir7, Priti Tagde8.
Abstract
In the light of thousands of infections and deaths, the World Health Organization (WHO) has declared the outbreak of coronavirus disease (COVID-19) a worldwide pandemic. It has spread to about 22 million people worldwide, with a total of 0.45 million expiries, limiting the movement of most people worldwide in the last 6 months. However, COVID-19 became the foremost health, economic, and humanitarian challenge of the twenty-first century. Measures intended to curb the pandemic of COVID-19 included travel bans, lockdowns, and social distances through shelter orders, which will further stop human activities suddenly and eventually impact the world and the national economy. The viral disease is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). After SARS-CoV-2 virus and Middle East respiratory syndrome (MERS)-related CoV, COVID-19 is the third most significant lethal disease to humans. According to WHO, COVID-19 mortality exceeded that of SARS and MERS since COVID-19 was declared an international public health emergency. Genetic sequencing has recently established that COVID-19 is close to SARS-CoV and bat coronavirus which has not yet been recognized as the key cause of this pandemic outbreak, its transmission, and human pathogen mechanism. This review focuses on a brief introduction of novel coronavirus pathogens, including coronavirus in humans and animals, its taxonomic classification, symptoms, pathogenicity, social impact, economic impact, and potential treatment therapy for COVID-19.Entities:
Keywords: COVID-19; Economy; Emerging pathogens; Novel coronavirus; Potential treatment; Social impact
Mesh:
Year: 2021 PMID: 34664166 PMCID: PMC8523003 DOI: 10.1007/s11356-021-16809-8
Source DB: PubMed Journal: Environ Sci Pollut Res Int ISSN: 0944-1344 Impact factor: 4.223
Fig. 1The symptoms of SARS-CoV-2
Fig. 2The illustrations of mink as a possible reservoir host of SARS-CoV-2 and transmission of CoV strain
Fig. 3Characteristics of Nidovirales
Fig. 4Structure of the coronavirus: (1) spike (S), (2) membrane protein (M), (3) envelope protein (E), (4) lipid bilayer, (5) nucleocapsid (N)
Classification of host, virus, disease, and cellular response classes of coronavirus
| Group | Host category | Name of the virus | Cellular responses | Types of disease | Reference |
|---|---|---|---|---|---|
| I (Animal pathogens) | Cat | Canine coronavirus, FeCoV, FIPV | Canine and feline APN | Respiratory, enteric and neurologic infection, and hepatitis | (Sood et al. |
| Pig | TGEV, PRCoV | Porcine APN | Respiratory and enteric infection | (Sood et al. | |
| Human | 229E and NL-63 | Human APN and ACE2 | Respiratory infections | (Ijaz et al. | |
| II (Veterinary pathogens) | Cow | BCoV | Neu5,9Ac2-containing moiety | Enteric infection | (Sood et al. |
| Human | OC43, HKU1, and SARS-CoV | Neu5,9Ac2-containing moiety | Respiratory infection, possibly enteric infection | (Saletti et al. | |
| Pig | Hemagglutinating encephalomyocarditis | Neu5,9Ac2-containing moiety | Respiratory, enteric and neurologic infection, and hepatitis | (Sood et al. | |
| Mouse | MHV | Murine CEACAM1 | Enteric and neurologic infection and hepatitis | (Miura et al. | |
| III (Avian pathogens) | Chicken | IBV | Not determined | Respiratory infection, hepatitis | (Dai & Gao |
| Turkey | Turkey coronavirus | Not determined | Respiratory and enteric infection | (Bayram et al. |
Fig. 5Illustration of coronavirus causing severe acute respiratory syndrome in animals
Antiviral medicines for COVID-19
| Intervention | Class | Type and mechanisms of action | Recommendations | Reference |
|---|---|---|---|---|
| Remdesivir | Antiviral | Remdesivir is a drug contact to combat the invasion of RNA polymerases | Tests in clinical studies | (M. F. Hossain et al. |
| Favipiravir | Antiviral | Favipiravir blocks viral polymerase RNA and thus stops viral replication | Completed clinical studies proved efficacy | (M. H. Rahman et al. |
| Convalescent plasma | Antiviral | Curated plasma contains defensive antibodies against SARS-CoV-2 | Confirmed effectiveness | (M. F. Hossain et al. |
| Lopinavir | Antiviral | HIV-approved protease inhibitors are lopinavir/ritonavir | Inconsistency in clinical trial findings | (Horby et al. |
| EIDD-2801 | Antiviral | Drives mutagenesis and impedes viral replication integration throughout RNA synthesis EDI-2801 | Clinical testing prepared | (M. H. Rahman et al. |
| Ritonavir | Antiviral | Ritonavir is HIV-approved protease inhibitor | Inconsistency in clinical trial findings | (Owa et al. |
| Ivermectin | Antiviral | To suppress the replication of the pseudorabies virus by inhibiting nuclear import of UL42 | Confirmed effectiveness | (Sharun, Dhama, et al. |
| Oseltamivir | Antiviral | Antiviral action is showed through selectively targeting conservative catalytic domain of RNA-dependent RNA polymerase (RdRp) | Completed clinical studies proved efficacy | (Rosa et al. |
| Umifenovir | Antiviral | To block the virus-cell membrane fusion | Completed clinical studies proved efficacy | (Pécheur et al. |
| Favipiravir | Antiviral | Antiviral action is showed through selectively targeting conservative catalytic domain of RdRp, interrupting nucleotide incorporation process amid viral RNA replication | Confirmed effectiveness | (Furuta et al. |
| GC376 | Protease inhibitor | Blocks virus replication | Confirmed effectiveness | (Sharun et al. |
| GC373 | Protease inhibitor | Blocks virus replication | Confirmed effectiveness | (Sharun et al. |
List of vaccines approved for their emergency use
| Vaccine | Type | Shot | Age group | Adverse effects |
|---|---|---|---|---|
| Pfizer-BioNTech | mRNA vaccine | 2 shots, 21 days apart | 16 and older | Chills, pain, headache, tiredness, and swelling at the injection site |
| Moderna | mRNA | 2 shots, 28 days apart | Adults 18 and older | Chills, pain, headache, tiredness, and swelling at injection site |
| Janssen | Viral vector | Single shot | Adults 18 and older | Fatigue, fever headache, injection site pain, or myalgia |
| Oxford-AstraZeneca | Viral vector | 2 shots, 4–12 weeks apart | Adults 18 and older | Tenderness, redness, pain, warmth, itching, swelling at the injection site |
| Novavax | Protein adjuvant | 2 shots, 3 weeks apart | 12–84 years old | Pain at the site of injection, fatigue, and fever |