Molecular Basis of the Structure and Transmission of SARS-CoV, SARS-CoV-2, and MERS: A Review Report

Saima Naz1*, Ahmad Manan Mustafa Chatha2, Durali DANABAS3, Aqsa Arshad4

1Department of Zoology, Government Sadiq College Women University, Bahawalpur, Pakistan

2 Department of Entomology, Faculty of Agriculture and Environment, The Islamia University of Bahawalpur, Pakistan

3 Munzur University, Fisheries Faculty, Tunceli, Turkey

4Institute of Zoology, University of the Punjab Lahore, Pakistan

ABSTRACT

In late 2019, a new coronaviridae family member officially designated as “Severe Acute Respiratory Syndrome Coronavirus-2” (SARS-CoV-2) emerged and began to spread intensely, worldwide. Its rapid spread was declared as a pandemic by the World Health Organization (WHO) in March 2020. Within the coronaviridae family, SARS-CoV-2 is the third highly pathogenic virus that infects human beings, following the Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) and the Middle East Respiratory Syndrome Coronavirus (MERS-CoV). In this review, the molecular basis for the origin, mode of action, invasion, and organization of these viruses are discussed by using various models.  Moreover, the transmission pathways, replication mechanisms, and diagnostic strategies of these viruses are also discussed. The molecular basis of SARS and MERS helps to understand their infection patterns, pathogenic mechanisms with anecdotes on their diagnosis, and future directions. Expectedly, this study would serve the purpose of being a reliable source of information to scientists, clinicians, as well as the general public.

GRAPHICAL ABSTRACT

Keywords: mode of transmission, severe acute respiratory syndrome (SARS), Middle East respiratory syndrome (MERS), pathogenic mechanisms, structural comparison

1. INTRODUCTION

Coronaviruses (enveloped, large RNA viruses, + single‐stranded) reportedly infect both human beings and animals. Tyrrell and Bynoe [1] were the first to describe these viruses in patients suffering from common cold. On the basis of their morphological characteristics, such as their projecting surface which shows their resemblance with the solar corona and their spherical virion, these viruses were named coronaviruses (Latin: corona = crown). Major sub families of these viruses include alpha‐, beta‐, gamma‐ and delta‐. Out of these four, alpha‐ and beta‐ emanate from mammals, particularly from bats. While, the rest of the two originate from pigs and birds. Its genome size varies between 26 kb and 32 kb. Among the above subtypes of these viruses, beta‐ SARS-CoV-2/coronaviruses cause fatalities and serious diseases, while alpha‐coronaviruses are known for asymptomatic or mildly symptomatic inflammations in human beings. Moreover, a new disease related to a novel coronavirus (COVID-19) was reported in 2019 and confirmed as a great threat to human health globally. Public health emergency of an international concern was declared by WHO in 2020. During the first two months of the outbreak, its epidemic spread was reported across the various countries around the world [2]. The general structure of human coronavirus is shown in Figure 1.

 

Figure 1. Structure of Human Coronavirus

1.1. Types of Coronaviruses

A huge family of viruses (COVs) cause respiratory and intestinal illnesses in both animals and humans [3, 4]. They were known for causing cold infections/pneumonia in human beings. The emergence of severe acute respiratory syndrome (SARS, 2002–2003) and Middle East respiratory syndrome (MERS, 2012) in China and the Arabian Peninsula, respectively caused life threatening health hazards. Since December 2019, the world has been combating another virus namely SARS-CoV-2, which is responsible for the current spread of COVID-19, identified first in Wuhan, China  following serious pneumonia [5, 6]. Besides SARS AND MERS, some other types of coronaviruses are also depicted in Table 1.

Table 1. Types of Coronaviruses

#

Corona Virus Types

Natural Reservoir

Intermediate Host

Mode of Transmission

Names of Vaccines

Target organ

Lethality

Rate (%)

Reference

1

SARS-CoV-2

Horseshoe bats

Palm civets

Airborne particles

i. SinoVac

ii. CoronaVac

iii. COVAXIN

Lungs, Kidney, nervous system,

15%

[8]

2

MERS

Egyptian tomb bat

Dromedary camel

Aerosols transmission

i. Ribavirin

ii. interferon-α2a

iii. Lopinavir/ritonavir

Lungs, Kidney, nervous system,

34%

[9]

3

SARS

Horseshoe bats

Palm Civets

Droplets, aerosols and contacts

i. Ribavirin

ii. Methylprednisoloe

iii. Interferons, Lopinavir

iv. ribavirin, Pentaglobin

Lungs, nervous system

1-3%

[10]

4

HCoV-OC43

Rodent associated virus

Cattle or Swine

Seasonal outbreak

i. Pfizer bioNTech (BNT 162b2)

ii. Moderna (mRNA1237)

Gastroenteritis and respiratory tract infection.

34.69%

[11]

5

HCOV-HKU1

Rodents

Domestic animals

Airborne particles

ELISA-based IgG antibody

Mild upper respiratory disease

0 to 4.4%

[12]

6

HCOV- NL63

Humans

Human

Droplets aerosols

Sera vaccine

Respiratory system

Up to 10 %

[13]

7

HCOV-229E

African Hipposiderid Bats

Camelids

Diarrhea

Corticosteroids

Lungs and digestive system

10--27%

[14]

1.2. Coronaviruses Found in Human Beings

Seven coronaviruses (HCoVs) have been identified in human beings [5]. Out of these seven, four are more common, known for their mild respiratory attacks and show comparatively low risk in healthy human beings. On the other hand, they cause chronic illnesses in people with a weak immune system. The other three (SARS-CoV, SARS-CoV-2, and MERS) cause difficulty in breathing, often leading to death. In comparative study, SARS-CoV-2 was determined to be relatively less severe than severe acute respiratory syndrome (SARS-CoV) and Middle East respiratory syndrome (MERS) in terms of the severity of the infection it causes (COVID-19) but more severe than four other HCoVs.[6] Transmission of this virus was reported to human beings from animals. SARS CoV-2, MERS, and SARS originally came from bats but now several researchers believe that pangolin act as intermediate host for the transfer of SARS-CoV-2 to humans from its host species [7]. In the current review study, a comparison of the major types of viruses namely SARS-CoV and MERS is made. In addition, transmission mode, targeted organs, vaccination, and mortality of coronavirus is specified in Table 1.

1.2.1. Sources of Coronaviruses. Genome studies demonstrated bats and pangolins as major reservoir for the spread of this virus [15]. Faecal oral route, aerosol (especially emitted out during clinical trials), coughing, mucosa membrane when come in contact with surfaces like clothing and sneezing are the main sources of viral spread from one individual to another [16].  The study also[17] reported viral RNA discernment in stools which showed GI symptoms along with the expression of angiotensin converting enzyme (2) (ACE 2) [18]. So far, no evidence regarding trans-placental and intrauterine mode of transmission of these viruses has been outlined [19, 20]

1.3. Severe Acute Respiratory Syndrome (SARS)

The first sign of disease related to SARS‐CoV was pneumonia which helped in case detection. Recently, symptoms (gastrointestinal) and infections (asymptomatic) were also reported in young children [21]. Incubation period of about 5 days with a mean period of incubation of 3 days (ranging in days between 0 to 24)) were suggested by [22]. However, clinical indications begin after days (less than a week) in symptomatic persons showing GIT, cough, fatigue and fever symptoms. On admission, about 75% of patients showed serious chest and dyspnea symptoms, detected by a computer-based tomography analysis. It was observed that pneumonia appears in the 2nd or 3rd week of symptomatic inflammation and its predominant signs include decline in O2 saturation level. These results were evident through various techniques, such as imaging techniques, illustrating deterioration along with consolidation and exudation of alveoli [22].

1.3.1. Types of Severe Acute Respiratory Syndrome (SARS). Severe Acute Respiratory Syndrome (SARS) is a viral respiratory illness caused by the SARS coronavirus (SARS-CoV). There is only one known strain of the SARS virus, which emerged in 2002 and caused a global outbreak. The World Health Organization (WHO) refers to this strain as ‘SARS-CoV-1’ to distinguish it from other related coronaviruses. The SARS outbreak in 2002-2003 resulted in significant morbidity and mortality with over 8,000 reported cases and nearly 800 deaths, worldwide. Since then, there have been no reported cases of SARS-CoV-1 transmission to humans. It is important to note that SARS-CoV-2, the virus responsible for the ongoing COVID-19 pandemic, is a distinct and separate virus from SARS-CoV-1. SARS-CoV-2 belongs to the same family of coronaviruses but is genetically different from the SARS-CoV-1 virus.

1.4. Severe Acute Respiratory Syndrome (SARS-CoV)

SARS-CoV is a type of coronavirus that causes the illness known as SARS. It is a member of the coronaviridae family, which also includes other types of coronaviruses. SARS-CoV is an enveloped, single-stranded RNA virus with a relatively large genome. Primarily, scientists focused on civets and raccoon dogs, considering them the main reservoir of infection in case of SARS-CoV. During an experimentation for viral RNA detection, isolated samples taken from food market having civets depicted positive outcomes,  showing civet palm as a secondary host [23]. Other researches also concluded bats as a source of viral replication in their study since Rhinolophus bats possess antibodies (anti-SARS-CoV) [24]. The virus infects cells in the respiratory system, leading to symptoms such as high fever, cough, difficulty breathing, and pneumonia. In 2012 in Saudi Arabia, the emergence of  MERS were first  reported [25] showing their pertinence to β-coronavirus and in their case camels act as zoonotic source [26]. As far as its major sources of transmission were concerned, middle east respiratory syndrome was also detected in  species of bats  named Perimyotis and Pipistrellu [27] indicating them as a basic host and transmitting medium [28 , 29]. Snakes may be possible host in their transference, but some novel findings proved this wrong.

1.5. Structure of SARS 

Genome of SARS-CoV includes 29,727 nucleotides (in length) having 11 ORFs. These include 1) specified location and number of small open reading frames, 2) having 1 copy of Polypro, and 3) short anchoring of S protein. Figure 2a gives the systematic representation of genome organization of SARS.

 

Figure 2a. Schematic Representation of Genome Organization and Functional Domains of S protein SARS-CoV

Spike glycoprotein of this virus is a membranous protein (type 1) and makes a trimer formation. It usually has a trans-membranous segment which helps the trimer to anchor the viral membrane. Further, ectodomain plays a role in decorating its virion surface. On the cell surface of the host, it mostly binds to ACE2 enzyme (receptor angiotensin- converting enzyme 2) which is a receptor present on the host’s surface resulting in membrane fusion, while undergoing various rearrangements related to the structure [15]. This glycoprotein is reported to be glycosylated heavily with each promotor having glycosylation sites (22N linked) [30]. Various studies regarding the initial analysis of the strain (Wuhan-Hu-1) which outbreaks confirmed to be  amino acid residues (1273), with N-terminus signal peptide, binding receptor fragment S1 as well as S2 (fusion fragment) in it. Moreover, S1 is further divided into a huge number of domains, such as NTD, CTD1, CTD2 and RBD (N-terminal domain, C- terminal domains 1 and 2 and receptor binding domain).

1.6. Severe Acute Respiratory Syndrome (SARS-CoV-2)

SARS-CoV-2, also known as Severe Acute Respiratory Syndrome Coronavirus 2, is the virus responsible for the global COVID-19 pandemic. It is a novel coronavirus that was first identified in late 2019 in Wuhan, China. SARS-CoV-2 belongs to the same family of viruses as SARS-CoV but they are distinct viruses with different characteristics. SARS-CoV-2 is a positive-sense, single-stranded RNA virus. It has a spike protein on its surface that enables it to enter and infect human cells, particularly cells in the respiratory system. The virus primarily spreads through respiratory droplets when an infected person coughs, sneezes, talks, or breathes heavily. It can also spread by touching contaminated surfaces.

1.7. Structure and Transmission of Severe Acute Respiratory Syndrome (SARS-CoV and SARS-CoV-2)

The fatality rates of pneumonia of SARS-CoV, SARS-CoV-2, and MERS-CoV (2.9, 9.6, and ∼36 percentages, respectively) were reported [31]. OC43, NL63, HKU1, and 229E (HCoV-s) also have the capability to cause diseases, although they are self-limited and show mild symptoms [32]. The general structure of SARS-CoV-2 is shown in Figure 2b.


Figure 2b.  Structure of SARS-CoV-2

1.8. Genome Organization of SARS-CoV and CoV-2

Genomic organization of severe acute respiratory syndrome corona virus 2 encodes four virally structural proteins named spike (S), envelope (E), membrane (M), and nucleocapsid (N) proteins 3–5, follow the characteristic gene order [5’ -replicase (rep gene), (S), (E), (M), (N)-3’] having un-translated short regions at both terminals (Figure 1). For virus to enter the host cells, the above mentioned proteins along with the spike protein play a fundamental functional role. Non-structural protein is encoded by rep gene and constitutes about 2/3 of genome at 50 ends. Thoroughly, S protein acts as an important therapeutic target as it is in charge of receptor-binding and subsequent viral entry into the host cells [33]. Literature reported the roles of M and E proteins in viral assembly; however, RNA synthesis is carried out by (nucleocapsid) protein. Figure 2c shows the non-structural proteins.

 

Figure 2c: Summary Diagram Illustrating the Non-Structural Proteins of Severe Acute Respiratory Syndrome (SARS)

Table 2. Role of Different Proteins in SARS

#

Name of Proteins

Coding Genes

Amino Acids

Role of Protein in SARS

References

1

Non-Structural Proteins

NSP1

180

NSP1 obstructs the ribosome entry site of host mRNA and hence prevents translation.

NSP1 inhibits the assembly of antiviral components in host’s cell.

[34-36]

N-Terminal product of Viral Replicase

2

N-Terminal product

NSP2

639

NSP2 contains a Glutamine at 131 amino acid that is involved in formation of Hydrogen bond and also enhances the durability of SARS Coronavirus.

[37, 38]

3

Papain-like Proteinase

NSP3

1946

NSP3 interacts the formation of interferons in the immune system of the host which results in malfunctioning of host’s Natural defense process against SARS-CoV-2.

[39, 40]

4

Membrane-spanning protein containing transmembrane domain 2

NSP4

501

NSP4 works in coordination with NSP3

NSP6 protein for formation of vesicle that acts as a site of replication of virus.

[41]

5

Proteinase and main proteinase

NSP5

307

NSP5 causes the cleavage of 11 different regions that release NSP4 to NSP16 in SARS-CoV-2 and is also involved in self-proteolysis.

[42, 43]

6

Putative Transmembrane domain

NSP6

291

Many features of autophagy induction by NSP6 suggested that the protein activates the omega some pathway normally used by cells to generate auto phagosomes from the ER in response to starvation.

[43, 44]

7

RNA-dependent RNA Polymerase

NSP7

84

A complex of NSP8 (next section) and NSP12, along with NSP7 is required in order for NSP8 to have RNA polymerase activity.

[44, 45]

8

Multimeric-RNA polymerase; replicase single-stranded

NSP8

199

NSP7 and NSP8 are catalytic NSP12 cofactors that are essential for a highly active NSP12 polymerase complex and have a role in the stability of NSP12 RNA binding regions.

NSP8 from human coronavirus 229E has been shown to be an oligo(U)-templated poly-adenyl-transferase with strong (mono/oligo) adenylate transferase activity. NSP8 has N-terminal and C-terminal D/Ex D/E conserved motifs. The N-terminal motif is critical for RNA polymerase activity as these residues are part of the Mg2-binding active site.

[44, 46-48]

9

RNA binding viral protein

NSP9

114

NSP9 plays major role in Coronavirus replication cycle.

NSP9 also interferes with many proteins that are important for producing viral replication complex.

[49]

10

A growth-factor-like protein with two zinc-binding motifs.

NSP10

140

NSP10 interacts with NSP16 and triggers its methyl transferase activity.

It results in the insertion of a cap at the 5' end of SARS-COV mRNA, preventing the host immune system from breaking down viral RNA via 3'-5' exonuclease activity.

[50]

11

RNA polymerase that is RNA dependent

NSP12

932

NSP12 is in charge of viral genome replication and transcription.

[51, 52]

12

RNA dependent

RNA Polymerase

(pol/Rd Rp)

NSP13

607

Cryo-electron microscopy investigations have recently revealed the architecture of the NSP13 replication and transcription complex, which contains two copies of NSP13 that engage with NSP8 via the N-terminal ZBD.

One of the NSP13 protomers interacts with NSP12 further and is placed in the route of downstream RNA with its RNA binding site.

[53]

13

Exoribonuclease domain

(Exon/NSP14)

NSP14

527

NSP14 -Exon is also involved in other viral life cycle processes, such as viral genome recombination and interference with host innate immune response.

Furthermore, the presence of NSP14-Exon may provide coronavirus specific resistance to nucleoside analogue medicines, posing a significant challenge to the development of NSP12(RNA-dependent polymerase)-targeted nucleoside inhibitors.

[54]

14

NSP15-AI and NSP15B-NendoU

NSP15

346

NSP15 is responsible for protein interference with the innate immune response; however, other investigations show that the mechanism is independent of endonuclease activity.

There is additional evidence that NSP15 degrades viral RNA in order to conceal it from host defense. Nonetheless, NSP15 is required for coronavirus biology.

[55]

15

2-o-ribose methyl transferase

NSP16

298

NSP16 play an essential role in coronavirus mRNA cap 2-o-ribose methylation and that the presence of N7-methyl guanosine is a prerequisite for NSP16 for binding. The purpose of this activity is one of the camouflages as a mean of evading detection by the host immune system.

[56]

16

Accessory Proteins

Induced double membrane vesicles

ORF3a

275

ORF3a is a Viroporin, an integral membrane protein that can act as an ion channel, potentially promoting virus release. Moreover, this protein interacts with caveolin potentially regulating different phase of viral cycle.

[57-59]

17

Spike protein

ORF6

61

SARS-CoV-2 orf6 showed the highest suppression on both primary interferon production and interferon signalling among the 27 viral proteins.

Orf6-deleted SARS-CoV-2 may be considered for the development of intranasal live-but-attenuated vaccine against COVID-19

[60,61]

18

Membrane protein

ORF7a

122

Their absence from other genomes implies that they may play specialized roles in SARS-COV replication, assembly, or virulence.

[62, 63]

19

Membrane protein

ORF7b

44

ORF7b's apoptosis-inducing function in cells. Cytokine levels and host innate immune responses were also studied, including the expression of interferon regulatory transcription factor (IRF)-3, signal transducer and activator of transcription (STAT)-1, interferon (IFN)-, tumors necrosis factor (TNF)-, and interleukin (IL)-6.

[64, 65]

20

Spike protein

ORF10

38

ORF10, which has been suggested to play a role in immune evasion. ORF10 overexpression significantly reduced the expression of type I interferon.

SARS-CoV-2-infected HeLa cells expressed genes and interferon-stimulated genes in vitro

[66]

 1.9. Transmission of SARS-CoV and CoV-2

The main sources of transmission are droplets and aerosols, with the respiratory route of transmission to be the most prevalent [67]. The authors [68] during their SARS-CoV-2 RNA detection in the stool of persons with COVID-19 pneumonia confirmed oral-fecal route as an active transmission source. So, biosorbents having a role in the inactivation of viruses should be examined [15]. The validation of RNA detection has been observed on mobile phone and door handle surfaces. This means that a person who comes in contact with these inanimate coverings and an infected persons may also have the chance of getting infection [69].

 Keeping in consideration vertical transmission, 9 pregnant women with confirm corona cases showed no mother to baby transmission. In addition, breastfeeding transmission was not proved as no severe acute respiratory syndrome was detected in milk of mother. During an experimentation, an infant with the highest level of IgM against this virus was given birth and after two hours delivery period IgM A.B with IgG A.B were analyzed in the newborn baby. PCR technique performed on nasopharyngeal swabs (consecutively) for a period of two hours – sixteen days showed negative results. The levels of Il-6 as well as IL-10 were also raised. So, a hypothesis can be made on the consideration that if IgM is not capable of crossing placenta and making its way towards fetus, then the newly born can be infected via in utero even if we cannot take amniotic fluid for SARS-CoV-2 RNA testing [70]. The mode of transmission of SARS is diagrammatically shown in Figure 2d.

 

Fig 2d. Mode of transmission of SARS (Boone and Gerba 2007)

1.10. Risk factors of SARS

Clinical studies confirmed that elderly people having SARS along with chronic illnesses are more vulnerable to complications due to their low immunity [71], reportedly the failure of organs and occasionally, death [72 ,73].

1.11. Structure and Transmission of Middle East Respiratory Syndrome (MERS)

Middle East respiratory syndrome (MERS) is a respiratory syndrome and dromedary camels are known to be their initial source of origin. As far as its transmission to humans is concerned, it is still not known. Its name shows that this viral disease is predominant in region of Middle East, in comparison with the other parts of the world [74].

1.11.1. Structure.

It is a norovirus enveloped and usually decorated with (S) glycoprotein homotrimers that facilitate its entry into the host cells. Studies demonstrated that spike (S) antigen is present on viral surface and acts as a target in the neutralization of antibodies and designing of vaccines. In cryogenic electron microscopy technique performed for S ectodomain trimers of related COVID-19 and MERS-CoV structures revealed snapshots of this fundamental protein in perfusion [75]. During encountering targeted cells or viral biogenesis, the cleavage of MERS coronavirus occurs at junction point found in between subunits (S1 and S2) [76]. Moreover, the 2nd cleavage site S2 is processed on onseting of fusion of membrane and is found in S2 subunit upstream of fusion peptide. Both of these cleavage sites enhanced chances of viral entry and in modulation of cell tropism and host range [77].

1.11.2. Organization of Genome. Genome size of this virus varies in its nucleotide length of about (30, 119), replication gene containing non-structural proteins named NSP1 to NSP16 and poly (A) tail at 50 and 30 end of genome, respectively. A cap structure of about 50 terminal as well as spike, enveloped, nucleocapsid and membrane structural proteins are also seen in their genome organization. Moving inside of its structure, four kinds of accessory proteins can be seen, arranged as ORF4a, ORF4b, ORF3, ORF5 and ORF8, constituting about 10 kilo base at genome 30 end. These viruses genome does not encode for a protein hemagglutinin-esterase unlike other β-coronaviruses [78]. Various kind of accessory proteins found in both viruses (MERS-CoV having 5 proteins and SARS-CoV having 8) proved to be helpful in evading immune system. The major differences might lead the way towards the signaling and induction of IFNs type 1 with greater sensitivity. Schematic representation of the genome organization of MERS is shown in (Figure 3 a). Further, the role of different protein in MERS is shown in Table 3.

 

Figure 3a. Schematic Representation of Genome Organization and Functional Domains of S Protein for MERS

Table 3. Role of different proteins of MERS

#

Name of Proteins

Coding Genes

#Amino Acids

Role of Protein in SARS

References

1.

Structural proteins

Envelope protein

ORF6

(Open reading frame 6)

82

Formation of the virion

Potential ion channel activity that participates in viral budding and releases B cell epitopes that could be significant.

[79]

2.

Membrane (M) protein

ORF 7

(Open reading frame 7)

131

Development of viral envelope.

viral core by Interrelate with N protein n virion assembly.

[80]

3

Nucleocapsid protein

ORF8a

(Open reading frame 8a)

413

Major elements of nucleocapsid structure.

It is necessary for the assembly of viral replication.

Also necessary for post-translational-modification. modulating the host’s initial innate response

[81]

4

Spike protein

ORF2

(Open reading frame 2)

1353

Help in virus entry it’s binding to receptor an also take part in fusion

[82]

5

Accessory proteins

Accessory protein (AP3)

ORF3

(Open reading frame 3)

232

Virus multiplication,

Disease-causing

[83]

6

Accessory protein

(AP 4a)

ORF4a

(Open reading frame 4a)

325

Viral replication

interferon (IRF) antagonism

protein kinase R (PKR) antagonism

[84]

7

Accessory protein

(AP 4b)

ORF4b(Open reading frame 4b)

246

Control of nuclear factor kappa B (NFK B)

[85]

8

Accessory protein (AP5)

ORF5

(Open reading frame 5)

201

IFN (interferon) virus ,

formation of NF KB initial inflammation

[86]

9

Accessory protein AP5

ORF5

(Open reading frame 5)

201

interferon (IRF) counteract

Inhibition of nuclear factor kappa B (NF-KB)

[87]

10

Nonstructural protein

NSP 1 coding region

NSP1

(non-structural protein

180

Identification of the viral RNA needed for effective viral multiplication.

[88]

11

Papain-like protease (PL-pro)

NSP3

(Nonstructural protein)

1945

It causes cleavage at positions 1-3 to produce three nonstructural proteins (NSPs).

detected by protease domain

Replication of viruses

membranous proliferation

IFN (interferon) antagonist

DE-ubiquitination

DE-phosphorylation

Splicing of t-RNA to ADP ribose

[89]

12

Domain of transmembrane

NSP4

(Nonstructural protein)

500

Viral multiplication membrane growth rapidly.

[40]

13

Main chymotrypsin-like or 3C-like protease (3CL pro)

NSP5

(Nonstructural protein)

197

Persistence of the virus

The protein that can be reproduced at a particular site is proteolytically processed, and 3CLpro cleaves the remaining site4-16 keys functional enzymes such as   helicase

[90]

14

Domain of transmembrane

NSP6

(Nonstructural protein)

3637 to 3923

Membrane development occurs quickly, and is linked to NSP3 and NSP4.

[91]

15

Primase

NSP8

(Nonstructural protein)

198

Primase activity

[92]

16

Methyl transferase inhibition

NSP10

(Nonstructural protein)

148

Membrane proliferation that controls 2-O-Mtase action

[93]

17

Helicase protein

NSP9

(non-structural protein)

113

Have binding activity with Ribonucleic acid, and Deoxyribonucleic acid in SARS COV

[94]

18

RNA dependent-RNA polymerase

NSP12

(Non structural protein)

932

Virus multiplication and its transcription

[95]

19

Superfamily 1 helicase

NSP13

(Non -structural protein)

601

Viral replication and also affects virulence and tropism

[96]

20

N-7 metyltransferase

Nidovirales

endoribonuclease

NSP15

(Nom -structural protein)

346

Viral replication

Exoribonuclease activity

[97]


1.11.3. Transmission.

Due to its stability in environmental conditions, its transmission is reported either through fomite or contact. In addition, transmission through fluid transfusions is also possible. As compared to SARS-CoV2, its transmission from one human being to another is limited. The major source of its transmission is debatable. The transmission chances of virus in humans through improperly cooked meat and milk were proved by RNA detection of MERS-CoV in camel’s milk. Bat to human transfer was also proposed recently and it might be possible that this transmission is either through intermediate or direct host.

A study majorly centered on epidemiology and transmissibility of MERS-CoV, showed that this virus does not reach its pandemic potential and its transfer from one individual to another is still limited. RT-PCR technique confirmed various cases in Jordan and Saudi Arabia from the time period of September 1, 2012 to June 15, 2013 and the main reason found was health care factors and nosocomial transmission.   The mode of transmission of MERS is depicted in (Figure 3b).

 

Figure 3b. Mode of transmission of MERS

1.11.4. Associated Risk Factors (MERS).

Different genders and different age groups have varying risk factors of infection by MERS. Men show a greater probability of infection as compared to women in most cases of outbreak [98].  Culture as well as customs also play an important key role as found that men in Arabian Peninsula are more exposed to camel handling than women [99].  In terms of age associated risk factors, elderly people (above 65 years of age) had a mortality ratio (8 to 9 times) higher than others [100]. Similarly, perople with immunosuppression problem, diabetes, hypertension, and heart failure are associated with an increase of fatality ratio (7 to 8 times) [101].

Detailed description of (MERS) entrance in cell, its replication and release are shown in (Figure 3c).

 

Figure 3c. Mechanism of MERS Entry, Replication and Release

Pathogenicity of MERS is initiated with the interaction of S protein with DPP4 receptor and virus entry through the respiratory tract. The expression of DPP4 begins in the respiratory tract in the following cell types (endothelial and epithelial cells, bronchial epithelial cells [non-ciliate] and hematopoietic cells) [85]. DPP4 is found in smaller number on upper airway surface as compared to alveoli and distal airways on epithelial cells [102]. So, their limited abundance ratio in upper airway may restrict their human transmission. Moreover, some other organ surfaces, such as intestine, thymus liver, and their tissues have DPP4 in a widely expressed form.

1.12. Comparative Study Analysis of SARS and MERS

1.12.1. Symptoms. The medical illustration of corona patients showed or ranged in from asymptomatic to respiratory syndrome and even death [103].  Clear demonstration is still not available but clinical studies reported some symptoms, such as fatigue, cough, pain, and fever. Among them, dry coughing, tiredness, and fever fall under the main symptoms of SARS-CoV-2, representing about 59%, 70%, and 99% respectively of the reported symptoms. The highest associated risk factors are usually associated with more aged people having underlying illnesses. Most importantly, almost similar reports with minute differences were found in case of MERS and SARS individuals. These resemblances might be an indication that all corona viruses follow almost the same mechanisms for their targeted areas or persons [104]. 

 Table 4. Comparison of SARS and MERS

Characteristics

SARS-COV

MERS-COV

Reference

Nucleotides length

29,727

30,119

[8]

Accessory protein

8

5

[107]

Spike protein

1255

1353

[108]

Non-structural protein(NSP)

At least 5

16

[78]

Structural protein

4

4

[109]

year of the initial case report

2019

2012

[110]

Pathway of dominant cell entrance

Unclear

Cell membrane fusion

[107]

Origin

zoonotic origin

zoonotic origin

[111]

Common transmission methods

Aerosol, Droplet, and contact

Aerosol, Droplet, and contact

[112]

Where the 1st case was reported

China

Middle east

[113]

Natural reservoir

Chinese horseshoe bats

Camels

[114]

Incubation time

4.3‐5.1 days;

5.0‐6.5 days

[115]

Death rates

~15%

34.4%

[116]

Vaccine

                                 i.  Ribavirin,

                  ii.  Methylprednisolone

                            iii.  interferons,

                              iv.  Lopinavir

                                v.  Ribavirin

                          vi.  Pentaglobin.

                                i.  Ribavirin

                        ii.  interferon-α2a

               iii.  Lopinavir/ritonavir,

            iv.  Convalescent plasma

[117]

An attribute's gene order

5’-replicase, ORF1ab,spike(S) envelope (E) membrane (M) and nucleocapsid (N)-3’

[118]

 

1.12.2. Diagnosis.

After diagnosis with COVID-19, the period of recovery differs depending upon their health condition and severity of symptoms. People with mild condition of this virus have chances to recover within a week. However, severe patients have to experience alveoli damage as well as respiratory failure, which may lead to death. The rate of mortality persists more in elder people having symptoms of serious diseases such as heart failure, Parkinson’s disease, and brain tumor [105].

1.12.3. Mortality Rate.

Death rates caused by coronaviruses, namely MERS-CoV and SARS-CoV reaches upto 37% and 10% -15%, respectively. COVID-19 patient’s death rate varied in between 2% to 4% and reached upto 13%, showing that death rate in case of COVID-19 is lesser than SARS and MERS [106]. Further comparisons are show in Table 4.

1.13.Treatment and Recovery

1.13.1. Treatment and Recovery of SARS (CoV and CoV-2)

1.13.1.1. Protein Subunit Vaccine. Protein subunits vaccines comprise virally antigenic fragments formed by recombinant techniques. In comparison with other viral vaccines, they are safer, can be produced easily, and are well tolerated. However, their low immunogenicity is their major drawback. Therefore, the usage of over stimulatory molecules for fusion are usually preferred to overcome this drawback. No clinical trials have been performed regarding protein subunit vaccines yet. However, in preclinical models, they showed protective effects as well as antibody responses. In a report by scientists, it was observed that S protein some specific characteristics, namely its full length, extracellular domain, and trimeric nature (tri spike) which have a role in immunity and evoke protection against infections caused by SARS-CoV-2.  Regarding S protein vaccines which are RBD based, it was observed that they have the potential for induction of high titer neutralizing AB with obvious pathogenic consequences. This is because of a lack of non-neutralizing epitopes which are mostly found in S protein type vaccines. In a report on mice models having confirmed SARS infection, this RBD based vaccine not only showed no viral RNA detection in lungs but also instigated antibodies (S- specific) that can be maintained for a duration of about one year.

1.13.1.2. Monoclonal Antibodies.

During outbreak and pandemic period of COVID-19, monoclonal antibodies types (Casirivimab-Imdevimab and Bamlanivimab) are licensed for protecting the suffering individuals usually having mild to moderate conditions. Further, their use as a diagnostic reagent is still under consideration that they may be proved beneficial if used as vaccines in the future.

1.13.1.3. Interferons.

For the treatment of viral inflammations that are emerging, interferons are used. IFNs belong to a class of immunomodulators which are manufactured by cells during the detection of specific pathogens that act upon stimulated neighboring cells.

1.13.2. Treatment and Recovery of MERS.  At present, the proper treatment for MERS-CoV is still not available. However, therapeutic course of action is under development [119]. Antiviral agents including interferons and alisporivir, immunotherapy, and immunoglobulins (intravenous) are used [120]. Therapeutic potential of various drugs and their efficacy in restoration against this MERS virus needs some clinical trials. As one preclinical study showed the reduction of mice weight when they were infected with convalescent serum (taken from immune camels) confirming its potential as a therapeutic agent [121].

Reports proved monoclonal and polyclonal ABs such as chimeric camel (novel) and heavy ABs (in case of humans) to be protective during outbreak management in various animals’ model species [122]. Among agents which are anti-viral only ribavirin (high dose treatment) showed significant efficacy against MERS-CoV infection in France and Saudi Arabia, while others like cyclosporine and interferons expressed inhibitory effects [123]. MERS showed more sensitivity towards interferon-α treatment. In a clinical analysis performed on the usage of various interferons, recombinants (lopinavir-ritonavir and beta-1b) showed lower mortality as compared to placebo among the patients suffering from this syndrome. Additionally, more significant outcomes were observed when treatment was given 7 days after symptoms appeared [124].

Another immunosupressor Mycophenolate mofetil (MMF) reportedly showed efficacy against MERS-CoV when its prescribed doses were injected to humans. When MMF was used in combination with IFN-β1b, a synergistic effect was seen [125]. Comparatively, using Marmoset’s models which are primates (non-human) developed wounds showed a higher fatality ratio as compared to animals that remained untreated [125]. Silvestro is a molecule found in plants family (fava line) and is reported to have the ability to bind with IFN-β1b and increases the affinity of eIF4A for messenger RNA. In response to this binding, helicase activity is blocked and protein translation is also inhibited. One in vitro report also supported anti-MERS coronavirus activity of this molecule. However, in vivo report studies regarding this molecule’s efficacy have not been conducted and established yet.

2. CONCLUSION

Several reports as studied above for SARS-CoV and MERS-CoV showed a number of similarities in various parameters like their mode of action, entrance, replication, vaccination methods and most importantly origin. Still, new methodologies need to be developed especially for their treatment and vaccination procedures. There should be proper campaigns, awareness methods, and health centers to guide young generation regarding its up regulation and shortcomings in near future. In addition, molecular data analysis regarding these emerging viruses still lacking a lot of mechanisms which could serve as a vehicle in better understanding of their emergence and how they invade the person’s immune system. So, reliable strategies should be developed by community working persons and scholars to manage this kind of pandemic emergency situations to avoid generation collapse in future.

REFERENCES

  1. Tyrrell D, Bynoe M. Cultivation of viruses from a high proportion of patients with colds. Lancet. 1966;287(7428):76-77. https://doi.org/10.1016/s0140-6736(66)92364-6
  2. Koehorst, J.J., et al., GISAID Global Initiative on Sharing All Influenza Data. Phylogeny of SARS-like betacoronaviruses including novel coronavirus (nCoV). Oxford, 2017. 34(8): p. 1401-1403.
  3. Kennelly JC, Lane MP, Barker JA, et al. Genotoxic activity of 1-chloromethylpyrene in stomach epithelium in vivo: insensitivity of the stomach scintillation UDS assay. Carcinogenesis. 1993;14(4):637-643. https://doi.org/10.1093/CARCIN%2F14.4.637
  4. Case AD, Darden T, Cheatham T, et al. AMBER 11, University of California, San Francisco. 2010. 2010.
  5. Wu F, Zhao S, Yu B, et al. Author Correction: A new coronavirus associated with human respiratory disease in China. Nature. 2020;580(7803):e7. https://doi.org/10.1038/s41586-020-2202-3
  6. Zhang S, Zhao J, Yao M. A comprehensive and comparative evaluation of primers for metabarcoding eDNA from fish. Methods Ecol Evol. 2020;11(12):1609-1625. https://doi.org/10.1111/2041-210X.13485
  7. Guan WJ, Ni ZY, Hu Y, et al. Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med. 2020;382(18):1708-1720. https://doi.org/10.1056/NEJMoa2002032
  8. Abdelrahman Z, Li M, Wang X. Comparative review of SARS-CoV-2, SARS-CoV, MERS-CoV, and influenza a respiratory viruses. Front Immunol. 2020;11. https://doi.org/10.3389/fimmu.2020.552909
  9. Raj VS, Farag EA, Reusken CB, et al. Isolation of MERS coronavirus from a dromedary camel, Qatar, 2014. Emerg Infect Dis. 2014;20(8):1339-1342. https://doi.org/10.3201%2Feid2008.140663
  10. Chan PKS, Chan MCW. Tracing the SARS-coronavirus. J Thorac Dis. 2013;5 Suppl 2(Suppl 2):S118-S121. https://doi.org/10.3978/j.issn.2072-1439.2013.06.19
  11. Grifoni A, Weiskopf D, Ramirez SI. et al. Targets of T Cell responses to SARS-CoV-2 coronavirus in humans with COVID-19 disease and unexposed individuals. Cell. 2020;181(7):1489-1501. https://doi.org/10.1016/j.cell.2020.05.015
  12. Bisht H, Roberts A, Vogel L, et al. Severe acute respiratory syndrome coronavirus spike protein expressed by attenuated vaccinia virus protectively immunizes mice. Proc Natl Acad Sci USA. 2004;101(17):6641-6646. https://doi.org/10.1073/pnas.0401939101
  13. Abdul-Rasool S, Fielding BC. Understanding human coronavirus HCoV-NL63. Open Virol J. 2010;4:76-84. https://doi.org/10.2174/1874357901004010076
  14. Ismail MM, Cho KO, Ward LA, Saif LJ, Saif YM. Experimental bovine coronavirus in turkey poults and young chickens. Avian Dis. 2001;45(1):157-163. https://doi.org/10.2307/1593023
  15. Zhou P, Yang XL, Wang XG, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. 2020;579(7798):270-273. https://doi.org/10.1038/s41586-020-2951-z
  16. Chen L, Zhong L. Genomics functional analysis and drug screening of SARS-CoV-2. Genes Dis. 2020;7(4):542-550. https://doi.org/10.1016/j.gendis.2020.04.002
  17. Rothan HA, Byrareddy SN. The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak. J Autoimmun. 2020;109:e102433. https://doi.org/10.1016/j.jaut.2020.102433
  18. Zhang H, Kang Z, Gong H, et al. The digestive system is a potential route of 2019-nCov infection: A bioinformatics analysis based on single-cell transcriptomes. bioRxiv. 2020. https://doi.org/10.1101/2020.01.30.927806
  19. Chen L, Zhong L. Genomics functional analysis and drug screening of SARS-CoV-2. Genes Dis. 2020;7(4):542-550. https://doi.org/10.1016/j.gendis.2020.04.002
  20. Schwartz DA. An analysis of 38 pregnant women with COVID-19, their newborn infants, and maternal-fetal transmission of SARS-CoV-2: Maternal coronavirus infections and pregnancy outcomes. Arch Pathol Lab Med. 2020;144(7):799-805. https://doi.org/10.5858/arpa.2020-0901-sa
  21. Chan JF, Lau SK, To KK, Cheng VC, Woo PC, Yuen KY. Middle East respiratory syndrome coronavirus: another zoonotic betacoronavirus causing SARS-like disease. Clin Microbiol Rev. 2015;28(2):465-522. https://doi.org/10.1128/cmr.00102-14
  22. Andersen KG, Rambaut A, Lipkin WI, Holmes EC, Garry RF. The proximal origin of SARS-CoV-2. Nat Med. 2020;26(4):450-452. https://doi.org/10.1038/s41591-020-0820-9.
  23. Kan B, Wang M, Jing H, et al. Molecular evolution analysis and geographic investigation of severe acute respiratory syndrome coronavirus-like virus in palm civets at an animal market and on farms. J Virol. 2005;79(18):11892-11900. https://doi.org/10.1128/JVI.79.18.11892-11900.2005
  24. Shi Z, Hu Z. A review of studies on animal reservoirs of the SARS coronavirus. Virus Res. 2008;133(1):74-87. https://doi.org/10.1016/j.virusres.2007.03.012
  25. Memish Z.A., Zumla A.I.,  Al-Hakeem R.F.,  Al-Rabeeah A.A.,  Stephens G.M., Family cluster of Middle East respiratory syndrome coronavirus infections. N Engl J Med. 2013;368(26): 2487-2494. https://doi.org/10.1056/nejmoa1303729
  26. Annan A, Baldwin HJ, Corman VM, et al. Human betacoronavirus 2c EMC/2012–related viruses in bats, Ghana and Europe. Emerg Infect Dis. 2013;19(3):456-459. https://doi.org/10.3201/eid1903.121503
  27. Huynh J, Li S, Yount B, et al. Evidence supporting a zoonotic origin of human coronavirus strain NL63. J Virol. 2012;86(23): 12816-12825. https://doi.org/10.1128/jvi.00906-12
  28. Lau SK, Li KS, Tsang AK, et al. Genetic characterization of Betacoronavirus lineage C viruses in bats reveals marked sequence divergence in the spike protein of pipistrellus bat coronavirus HKU5 in Japanese pipistrelle: Implications for the origin of the novel Middle East respiratory syndrome coronavirus. J Virol. 2013;87(15):8638-8650. https://doi.org/10.1128%2FJVI.01055-13
  29. Lu R, Zhao X,  Li J, et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: Implications for virus origins and receptor binding. Lancet. 2020;395(10224):565-574. https://doi.org/10.1016/S0140-6736(20)30251-8
  30. Watanabe Y, Allen JD, Wrapp D, Mclellan JS, Crispin M. Site-specific glycan analysis of the SARS-CoV-2 spike. Science. 2020;369(6501):330-333. https://doi.org/10.1126/science.abb9983
  31. Azhar EI, Hui DS, Memish ZA, Drosten C, Zumla A. The middle east respiratory syndrome (MERS). Infect Dis Clin North Am. 2019;33(4):891-905. https://doi.org/10.1016/j.idc.2019.08.001
  32. Corman VM, Muth D, Niemeyer D, Drosten C. Hosts and sources of endemic human coronaviruses. Adv Virus Res. 2018;100:163-188. https://doi.org/10.1016/bs.aivir.2018.01.001
  33. Du L, Yang Y, Zhou Y, Lu L, Li F, Jiang S. MERS-CoV spike protein: A key target for antivirals. Expert Opin Ther Targets. 2017;21(2):131-143. https://doi.org/10.1080/14728222.2017.1271415
  34. Subissi L, Posthuma CC, Collet A, et al. One severe acute respiratory syndrome coronavirus protein complex integrates processive RNA polymerase and exonuclease activities. Biol Sci. 2014;111(37):E3900-E3909. https://doi.org/10.1073/pnas.1323705111
  35. Bai Y, Yao L, Wei T, et al. Presumed asymptomatic carrier transmission of COVID-19. JAMA. 2020;323(14):1406-1407. https://doi.org/10.1001/jama.2020.2565
  36. Huang C, Lokugamage KG, Rozovics JM, Narayanan K, Semler BL, Makino S. SARS coronavirus nsp1 protein induces template-dependent endonucleolytic cleavage of mRNAs: Viral mRNAs are resistant to nsp1-induced RNA cleavage. PLoS Pathog. 2011;7(12):e1002433. https://doi.org/10.1371/journal.ppat.1002433
  37. Angeletti S, Benvenuto D, Bianchi M, Giovanetti M, Pascarella S, Ciccozzi M. COVID‐2019: The role of the nsp2 and nsp3 in its pathogenesis. J Med Virol. 2020;92(6):584-588. https://doi.org/10.1002/jmv.25719
  38. Cornillez-Ty CT, Liao L, Yates JR, Kuhn P, Buchmeier MJ. Severe acute respiratory syndrome coronavirus nonstructural protein 2 interacts with a host protein complex involved in mitochondrial biogenesis and intracellular signaling. J Virol. 2009;83(19):10314-10318. https://doi.org/10.1128/jvi.00842-09
  39. Khan MT, Zeb MT, Ahsan H, et al. SARS-CoV-2 nucleocapsid and Nsp3 binding: An in silico study. Arch Microbiol. 2021;203(1):59-66. https://doi.org/10.1007%2Fs00203-020-01998-6
  40. Lei J, Kusov Y, Hilgenfeld R. Nsp3 of coronaviruses: Structures and functions of a large multi-domain protein. Antiviral Res. 2018;149:58-74. https://doi.org/10.1016/j.antiviral.2017.11.001
  41. Hagemeijer MC, Ulasli M, Vonk AM, Reggiori F, Rottier PJ, De Haan CA. Mobility and interactions of coronavirus nonstructural protein 4. J Virol. 2011;85(9):4572-4577. https://doi.org/10.1128/jvi.00042-11
  42. Yang H, Xie W, Xue X, et al. Design of wide-spectrum inhibitors targeting coronavirus main proteases. PLoS Biol. 2005;3(11):e428. https://doi.org/10.1371/journal.pbio.0030324
  43. Cottam EM, Whelband MC, Wileman T. Coronavirus NSP6 restricts autophagosome expansion. Autophagy. 2014;10(8):1426-41. https://doi.org/10.4161/auto.29309
  44. Velthuis AJT, Worm SHVD, Snijder EJ. The SARS-coronavirus nsp7+nsp8 complex is a unique multimeric RNA polymerase capable of both de novo initiation and primer extension. Nucleic Acids Res. 2012;40(4):1737-1747. https://doi.org/10.1093/nar/gkr893
  45. Shi Z, Gao H, Bai XC, Yu H. Cryo-EM structure of the human cohesin-NIPBL-DNA complex. Science. 2020;368(6498):1454-1459. https://doi.org/10.1126/science.abb0981
  46. Kirchdoerfer RN, Ward AB. Structure of the SARS-CoV nsp12 polymerase bound to nsp7 and nsp8 co-factors. Nat Commun. 2019;10(1):e2342. https://doi.org/10.1038/s41467-019-10280-3
  47. Tvarogová J, Madhugiri R, Bylapudi G, Ferguson LJ, Karl N, Ziebuhr J. Identification and characterization of a human coronavirus 229E nonstructural protein 8-associated RNA 3'-terminal adenylyltransferase activity. J Virol. 2019;93(12):e00291-19. https://doi.org/10.1128/jvi.00291-19
  48. Yadav R, Chaudhary JK, Jain N, et al. Role of structural and non-structural proteins and therapeutic targets of SARS-CoV-2 for COVID-19. Cells. 2021;10(4):e821. https://doi.org/10.3390/cells10040821
  49. Sutton G, Fry E, Carter L, et al. The nsp9 replicase protein of SARS-coronavirus, structure and functional insights. Structure. 2004;12(2):341-53. https://doi.org/10.1016/j.str.2004.01.016
  50. Bouvet M, Imbert I, Subissi L, Gluais L, Canard B, Decroly E. RNA 3'-end mismatch excision by the severe acute respiratory syndrome coronavirus nonstructural protein nsp10/nsp14 exoribonuclease complex. Proc Natl Acad Sci USA. 2012;109(24):9372-9377. https://doi.org/10.1073/pnas.1201130109
  51. Kirchdoerfer RN, Ward AB. Structure of the SARS-CoV nsp12 polymerase bound to nsp7 and nsp8 co-factors. Nat Commun. 2019;10(1):e2342. https://doi.org/10.1038/s41467-019-10280-3
  52. Dominguez Andres, A., et al., SARS-CoV-2 ORF9c Is a Membrane-Associated Protein that Suppresses Antiviral Responses in Cells. 2020: p. 2020.08.18.256776. https://doi:10.1101/2020.08.18.256776
  53. Yan L, Zhang Y, Ge J, et al. Architecture of a SARS-CoV-2 mini replication and transcription complex. Nat Commun. 2020;11:e5874. https://doi.org/10.1038/s41467-020-19770-1
  54. Gribble J, Stevens LJ, Agostini ML, et al. The coronavirus proofreading exoribonuclease mediates extensive viral recombination. PLoS Pathog. 2021;17(1):e1009226. https://doi.org/10.1371/journal.ppat.1009226
  55. Deng X, Hackbart M, Mettelman RC, et al. Coronavirus nonstructural protein 15 mediates evasion of dsRNA sensors and limits apoptosis in macrophages. Proc Natl Acad Sci USA. 2017;114(21):e4251-e4260. https://doi.org/10.1073/pnas.1618310114
  56. Wang Y, Sun Y, Wu A, et al. Coronavirus nsp10/nsp16 methyltransferase can be targeted by nsp10-derived peptide in vitro and in vivo to reduce replication and pathogenesis. J Virol. 2015;89(16):8416-8427. https://doi.org/10.1128/jvi.00948-15
  57. Tomaszewski T, Devries RS, Dong M, et al. New pathways of mutational change in SARS-CoV-2 proteomes involve regions of intrinsic disorder important for virus replication and release. Evol Bioinform. 2020;16:1-18. https://doi.org/10.1177/1176934320965149
  58. Kern DM, Sorum B, Mali SS, et al. Cryo-EM structure of the SARS-CoV-2 3a ion channel in lipid nanodiscs. bioRxiv. 2021:573–582. https://doi.org/10.1101/2020.06.17.156554
  59. Nelson CW, Ardern Z, Goldberg TL, et al. Dynamically evolving novel overlapping gene as a factor in the SARS-CoV-2 pandemic. Elife. 2020;9:e59633. https://doi.org/10.7554%2FeLife.59633
  60. Yuen CK, Lam JY, Wong WM., et al., SARS-CoV-2 nsp13, nsp14, nsp15 and orf6 function as potent interferon antagonists. Emerg Microbes Infect. 2020;9(1):1418-1428. https://doi.org/10.1080/22221751.2020.1780953
  61. Gunalan V, Mirazimi A, Tan YJ. A putative diacidic motif in the SARS-CoV ORF6 protein influences its subcellular localization and suppression of expression of co-transfected expression constructs. BMC Res Notes. 2011;4:e446. https://doi.org/10.1186/1756-0500-4-446
  62. de Haan, C.A., et al., Coronaviruses as vectors: position dependence of foreign gene expression. J Virol, 2003. 77(21): p. 11312-23.
  63. De Haan CAM, Genne LV, Stoop JN, Volders H, Rottier PJ. Coronaviruses as vectors: Position dependence of foreign gene expression. J Virol. 2003;77(21):11312-11323. https://doi.org/10.1128/jvi.77.21.11312-11323.2003
  64. Morante S, Penna LG, Rossi G, Stellato FJFIMB. SARS-CoV-2 virion stabilization by Zn binding. Front Mol Biosci. 2020;7:e222. https://doi.org/10.3389/fmolb.2020.00222
  65. Yang R, Zhao Q, Rao J, et al. SARS-CoV-2 accessory protein ORF7b mediates tumor necrosis factor-α-induced apoptosis in cells. Front Microbiol. 2021;12:e654709. https://doi.org/10.3389/fmicb.2021.654709
  66. Schaecher SR, Mackenzie JM, Pekosz AJJOV. The ORF7b protein of severe acute respiratory syndrome coronavirus (SARS-CoV) is expressed in virus-infected cells and incorporated into SARS-CoV particles. J Virol. 2007;81(2):718-731. https://doi.org/10.1128/JVI.01691-06
  67. Bojkova D, Klann K, Koch B, et al. Proteomics of SARS-CoV-2-infected host cells reveals therapy targets. Nature. 2020;583(7816):469-472. https://doi.org/10.1038/s41586-020-2332-7
  68. Leung NHL, Chu DKW, Shiu EYC, et al. Respiratory virus shedding in exhaled breath and efficacy of face masks. Nat Med. 2020;26(5):676-680. https://doi.org/10.1038/s41591-020-0843-2
  69. Memish ZA, Alsahly A, Masri MA, et al. Sparse evidence of MERS‐C o V infection among animal workers living in Southern Saudi Arabia during 2012. Influenza Other Respir Viruses. 2015;9(2):64-67. https://doi.org/10.1111%2Firv.12287
  70. Han Q, Lin Q, Ni Z, You L. Uncertainties about the transmission routes of 2019 novel coronavirus. Influenza Other Respir Viruses. 2020;14(4):470-471. https://doi.org/10.1111/irv.12735
  71. Chen H, Guo J, Wang C, et al. Clinical characteristics and intrauterine vertical transmission potential of COVID-19 infection in nine pregnant women: A retrospective review of medical records. Lancet. 2020;395(10226):809-815. https://doi.org/10.1016/s0140-6736(20)30360-3
  72. Richardson CR, Franklin B, Moy ML, Jackson EA. Advances in rehabilitation for chronic diseases: Improving health outcomes and function. BMJ. 2019;365:el2191. https://doi.org/10.1136/bmj.l2191
  73. Harrison SL, Fazio-Eynullayeva E, Lane DA, Underhill P, Lip GY. Comorbidities associated with mortality in 31,461 adults with COVID-19 in the United States: A federated electronic medical record analysis. PLoS Med. 2020;17(9):e1003321. https://doi.org/10.1371%2Fjournal.pmed.1003321
  74. Kontis V, Mathers CD, Rehm J, et al. Contribution of six risk factors to achieving the 25× 25 non-communicable disease mortality reduction target: A modelling study. Lancet. 2014;384(9941):427-437. https://doi.org/10.1016/S0140-6736(14)60616-4
  75. Memish ZA, Perlman S, Van Kerkhove MD, Zumla A. Middle East respiratory syndrome. Lancet. 2020;395(10229):1063-1077. https://doi.org/10.1016/S0140-6736(19)33221-0
  76. Gui M, Song W, Zhou H, et al. Cryo-electron microscopy structures of the SARS-CoV spike glycoprotein reveal a prerequisite conformational state for receptor binding. Cell Res. 2017;27(1):119-129. https://doi.org/10.1038/cr.2016.152
  77. Park JW, Lee KJ, Lee KH, et al. Hospital outbreaks of middle east respiratory syndrome, Daejeon, South Korea, 2015. Emerg Infect Dis. 2017;23(6):898-905. https://doi.org/10.3201%2Feid2306.160120
  78. Millet JK, Whittaker GR. Host cell entry of Middle East respiratory syndrome coronavirus after two-step, furin-mediated activation of the spike protein. Proc Natl Acad Sci USA. 2014;111(42):15214-15219. https://doi.org/10.1073/pnas.1407087111
  79. Yin Y, Wunderink RG. MERS, SARS and other coronaviruses as causes of pneumonia. Respirology. 2018;23(2):130-137. https://doi.org/10.1111/resp.13196
  80. Surya W, Li Y, Verdià-Bàguena C, Aguilella VM, Torres J. MERS coronavirus envelope protein has a single transmembrane domain that forms pentameric ion channels. Virus Res. 2015;201:61-66. https://doi.org/10.1016/j.virusres.2015.02.023
  81. Forni D, Cagliani R, Clerici M, Sironi M. Molecular evolution of human coronavirus genomes. Trends Microbiol. 2017;25(1):35-48. https://doi.org/10.1016/j.tim.2016.09.001
  82. Lin SC, Ho CT, Chuo WH, Li S, Wang TT, Lin CC. Effective inhibition of MERS-CoV infection by resveratrol. BMC Infect Dis. 2017;17(1):e144. https://doi.org/10.1186/s12879-017-2253-8
  83. Li F, Li W, Farzan M, Harrison SC. Structure of SARS coronavirus spike receptor-binding domain complexed with receptor. Science. 2005;309(5742):1864-1868. https://doi.org/10.1126/science.1116480
  84. Liu J, Sun Y, Qi J, et al. The membrane protein of severe acute respiratory syndrome coronavirus acts as a dominant immunogen revealed by a clustering region of novel functionally and structurally defined cytotoxic T-lymphocyte epitopes. J Infect Dis. 2010;202(8):1171-1180. https://doi.org/10.1086/656315
  85. >Menachery VD, Mitchell HD, Cockrell AS, et al. MERS-CoV accessory ORFs play key role for infection and pathogenesis. mBio. 2017;8(4):e00665. https://doi.org/10.1128/mBio.00665-17
  86. Terada Y, Kawachi K, Matsuura Y, Kamitani W. MERS coronavirus nsp1 participates in an efficient propagation through a specific interaction with viral RNA. Virology. 2017;511:95-105. https://doi.org/10.1016/j.virol.2017.08.026
  87. Oudshoorn D, Rijs K, Limpens R, et al. Expression and cleavage of Middle East respiratory syndrome coronavirus nsp3-4 polyprotein induce the formation of double-membrane vesicles that mimic those associated with coronaviral RNA replication. mBio. 2017;8(6):e01658. https://doi.org/10.1128/mBio.01658-17
  88. Báez-Santos YM, John SES, Mesecar AD. The SARS-coronavirus papain-like protease: structure, function and inhibition by designed antiviral compounds. Antiviral Res. 2015;115:21-38. https://doi.org/10.1016/j.antiviral.2014.12.015
  89. Angelini MM, Akhlaghpour M, Neuman BW, Buchmeier MJ. Severe acute respiratory syndrome coronavirus nonstructural proteins 3, 4, and 6 induce double-membrane vesicles. mBio. 2013;4(4):e00524-13. https://doi.org/10.1128/mBio.00524-13
  90. Chan JF, Lau SK, To KK, Cheng VC, Woo PC, Yuen KY. Middle East respiratory syndrome coronavirus: another zoonotic betacoronavirus causing SARS-like disease. Clin Microbiol Rev. 2015;28(2):465-522. https://doi.org/10.1128/CMR.00102-14
  91. Aouadi W, Blanjoie A, Vasseur JJ, Debart F, Canard B, Decroly E. Binding of the methyl donor s-adenosyl-l-methionine to Middle East respiratory syndrome coronavirus 2'-O-Methyltransferase nsp16 promotes recruitment of the allosteric activator nsp10. J Virol. 2017;91(5):e02217-16. https://doi.org/10.1128/jvi.02217-16
  92. Kandeel M, Altaher A. Synonymous and biased codon usage by MERS CoV papain-like and 3CL-proteases. Biol Pharm Bull. 2017;40(7):1086-1091. https://doi.org/10.1248/bpb.b17-00168
  93. Deng X, Hackbart M, Mettelman RC, et al. Coronavirus nonstructural protein 15 mediates evasion of dsRNA sensors and limits apoptosis in macrophages. Proc Natl Acad Sci USA. 2017;114(21):e4251-e4260. https://doi.org/10.1073/pnas.1618310114
  94. Adedeji AO, Lazarus H. Biochemical characterization of Middle East respiratory syndrome coronavirus helicase. mSphere. 2016;1(5):e00235-16.
  95. https://doi.org/10.1128/mSphere.00235-16 Wippich F, Bodenmiller B, Trajkovska MG, Wanka S, Aebersold R, Pelkmans L. Dual specificity kinase DYRK3 couples stress granule condensation/dissolution to mTORC1 signaling. Cell. 2013;152(4):791-805. https://doi.org/10.1016/j.cell.2013.01.033
  96. Kim K, Tandi T, Choi JW, Moon J, Kim M. Middle East respiratory syndrome coronavirus (MERS-CoV) outbreak in South Korea, 2015: epidemiology, characteristics and public health implications. J Hosp Infect. 2017;95(2):207-213.
  97. https://doi.org/10.1016/j.jhin.2016.10.008Sha J, Li Y, Chen X, et al. Fatality risks for nosocomial outbreaks of Middle East respiratory syndrome coronavirus in the Middle East and South Korea. Arch Virol. 2017;162(1):33-44. https://doi.org/10.1007/s00705-016-3062-x
  1. Thabet F, Chehab M, Bafaqih H, Almohaimeed S. Middle East respiratory syndrome coronavirus in children. Saudi Med J. 2015;36(4):484-486. https://doi.org/10.15537%2Fsmj.2015.4.10243
  2. Alraddadi BM, Watson JT, Almarashi A, et al. Risk factors for primary Middle East respiratory syndrome coronavirus illness in humans, Saudi Arabia, 2014. Emerg Infect Dis. 2016;22(1):49-55. https://doi.org/10.3201/eid2201.151340
  3. Memish Z, Al-Tawfiq J, Makhdoom H, et al. Screening for Middle East respiratory syndrome coronavirus infection in hospital patients and their healthcare worker and family contacts: A prospective descriptive study. Clin Microbiol Infect. 2014;20(5):469-474.https://doi.org/10.1111/1469-0691.12562 
  4. Lupia T, Scabini S, Pinna SM, Perri GD, Rosa FGD, Corcione S. 2019 novel coronavirus (2019-nCoV) outbreak: A new challenge. J Glob Antimicrob Resist. 2020;21:22-27. https://doi.org/10.1016/j.jgar.2020.02.021
  5. Huang C, Wang Y, Li X, et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395(10223):497-506. https://doi.org/10.1016/S0140-6736(20)30183-5
  6. Espinosa OA, Zanetti ADS, Antunes EF, Longhi FG, Matos TAD, Battaglini PF. Prevalence of comorbidities in patients and mortality cases affected by SARS-CoV2: A systematic review and meta-analysis. Rev Inst Med Trop Sao Paulo. 2020;62:e43. https://doi.org/10.1590%2FS1678-9946202062043
  1. Perlman S. Another decade, another coronavirus. N Engl J Med. 2020;382(8):760-762. https://doi.org/10.1056/nejme2001126
  2. Song Z, Xu Y, Bao L, et al. From SARS to MERS, thrusting coronaviruses into the spotlight. Viruses. 2019;11(1):e59. https://doi.org/10.3390/v11010059
  3. Marra MA, Jones SJ, Astell CR, et al. The Genome sequence of the SARS-associated coronavirus. Science. 2003;300(5624):1399-1404. https://doi.org/10.1126/science.1085953
  4. Rota PA, Oberste MS, Monroe SS, et al. Characterization of a novel coronavirus associated with severe acute respiratory syndrome. Science. 2003;300(5624):1394-1399. https://doi.org/10.1126/science.1085952
  5. Luo GG, Gao SJ. Global health concerns stirred by emerging viral infections. J Med Virol. 2020;92(4):399-400. https://doi.org/10.1002/jmv.25683
  6. Al-Tawfiq JA, Zumla A, Memish ZA. Travel implications of emerging coronaviruses: SARS and MERS-CoV. Travel Med Infect Dis. 2014;12(5):422-428.  https://doi.org/10.1016/j.tmaid.2014.06.007 
  7. Addleman S, Leung V, Asadi L, Sharkawy A, Mcdonald J. Mitigating airborne transmission of SARS-CoV-2. Can. Med. Assoc. J. 2021;193(26):E1010-E1011. https://doi.org/10.1503/cmaj.210830
  8. Masood N, Malik SS, Raja MN, Mubarik S, Yu C. Unraveling the epidemiology, geographical distribution, and genomic evolution of potentially lethal coronaviruses (SARS, MERS, and SARS CoV-2). Front Cell Infect Microbiol. 2020;10:e499. https://doi.org/10.3389/fcimb.2020.00499
  9. Gong SR, Bao LL. The battle against SARS and MERS coronaviruses: Reservoirs and Animal Models. Animal Model Exp Med. 2018;1(2):125-133. https://doi.org/10.1002/ame2.12017
  1. Jiang X, Rayner S, Luo MH. Does SARS-CoV-2 has a longer incubation period than SARS and MERS? J Med Virol. 2020;92(5):476-478. https://doi.org/10.1002/jmv.25708
  2. Aleebrahim-Dehkordi, E., et al., Human Coronaviruses SARS-CoV, MERS-CoV, and SARS-CoV-2 in Children. J Pediatr Nurs. 2021. 56: p. 70-79. https://doi: 10.1016/j.pedn.2020.10.020
  3. Li YD, Chi WY, Su JH, Ferrall L, Hung CF, Wu TC. Coronavirus vaccine development: From SARS and MERS to COVID-19. J Biomed Sci. 2020;27:e104. https://doi.org/10.1186/s12929-020-00695-2
  4. Du L, He Y, Zhou Y, Liu S, Zheng BJ, Jiang S. The spike protein of SARS-CoV — a target for vaccine and therapeutic development. Nat Rev Microbiol. 2009;7(3):226-236. https://doi.org/10.1038/nrmicro2090
  5. de Wit E, van Doremalen N, Falzarano D, Munster VJ. SARS and MERS: Recent insights into emerging coronaviruses. Nat Rev Microbiol. 2016;14(8):523-534. https://doi.org/10.1038/nrmicro.2016.81
  6. Mustafa S, Balkhy H, Gabere MN. Current treatment options and the role of peptides as potential therapeutic components for Middle East Respiratory Syndrome (MERS): A review. J Infect Public Health. 2018;11(1):9-17. https://doi.org/10.1016/j.jiph.2017.08.009
  7. Mariamenatu AH, Abdu EM. Convalescent plasma as a therapeutic agent for SARS-CoV, MERS-CoV and SARS-CoV-2: A scoping review. J Acute Dis. 2021;10(2):47-56. https://doi.org/10.4103/2221-6189.312152
  8. Andreano E, Nicastri E, Paciello I. Extremely potent human monoclonal antibodies from COVID-19 convalescent patients. Cell. 2021;184(7):1821-1835. https://doi.org/10.1016/j.cell.2021.02.035.
  9. Rabaan AA, Ahmed SHA, Shah R, et al. MERS-CoV: Epidemiology, molecular dynamics, therapeutics, and future challenges. Ann Clin Microbiol Antimicrob. 2021;20(1):e8. https://doi.org/10.1186/s12941-020-00414-7
  10. Malhani AA, Enani MA, Askari FSS, et al. Combination of (interferon beta-1b, lopinavir/ritonavir and ribavirin) versus favipiravir in hospitalized patients with non-critical COVID-19: A cohort study. PLoS One. 2021;16(6):e0252984. https://doi.org/10.1371/journal.pone.0252984
  11. Liatsos GD. Controversies' clarification regarding ribavirin efficacy in measles and coronaviruses: Comprehensive therapeutic approach strictly tailored to COVID-19 disease stages. World J Clin Cases. 2021;9(19):5135-5178. https://doi.org/10.12998/wjcc.v9.i19.5135
  12. Millet JK, Whittaker GR, Host cell proteases: Critical determinants of coronavirus tropism and pathogenesis. Virus Res. 2015;202:120-134. https://doi.org/10.1016/j.virusres.2014.11.021
  13. Yang Y, Zhang L, Geng H, et al. The structural and accessory proteins M, ORF 4a, ORF 4b, and ORF 5 of Middle East respiratory syndrome coronavirus (MERS-CoV) are potent interferon antagonists. Protein Cell. 2013;4(12):951-961. https://doi.org/10.1007/s13238-013-3096-8

 

 

 

* Corresponding Author: saima.naz@gscwu.edu.pk