Monkeypox virus has evolved into two separate clades: West Africa and Congo Basin ^[1][12]. Different epidemiological and clinical characteristics distinguish the diseases caused by the two MPXV clades. The Congo Basin strain has a fatality rate of 10% ^[2][13]. West Africa has a fatality rate of approximately 1%, with a higher mortality rate among patients with HIV co-infection ^[3][14]. From 1986 to 1992, only 13 incidents were reported of monkeypox, and none were recorded from 1993 to 1995 ^[4][15]. In 1997, a total of 88 individuals were confirmed to have monkeypox (MPX) infection, whereas in 1996, there was a sudden increase in the number of MPXV-infected human cases reported in  Democratic Republic of the Congo (DRC) ^[4][5]RC [15,16]. MPX outbreak occurred in the United States in 2003. This is the first outbreak of MPX outside of Africa, and it has been linked to the importation of marmots from Africa into the United States. A total of 47 people have been detected in five states ^[6][7][17,18]. From September to December of 2005, Sudan reported ten confirmed cases and nine suspected cases of MPXV due to an outbreak of MPX ^[8][19]. Between 2006 and 2007, human MPX infection was again detected in DRC. Since the 1980s, MPX transmission has increased by 20, while smallpox vaccination reduces disease risk by 21 ^[9][20].

In addition, monkeypox from Central Africa inhibits T-cell receptor-mediated activation, suppressing proinflammatory cytokine production within human cells from earlier infected monkeypox patients ^[10][21]. The MPXV inhibitor supplementing the enzymes or gene inhibits enzymes missing in West African strains and has been recognized as an essential immune modulating factor contributing to the increased virulence of Central African strains ^[11][22]. Additionally, the central African strain selectively regulates host responses, particularly in host cell death ^[12][23]. Infection with central African monkeypox appears to preferentially inhibit the transcription of genes essential in host immunity, according to transcriptional research ^[9][13][20,24].

The Orthopoxvirus genus of the Poxviridae family includes numerous zoonotic infections, particularly monkeypox ^[14][25]. To replace monkeypox, the WHO will adopt the new preferred name, “Mpox” ^[15][26]. Poxviruses’ primary hosts are lemmings, rabbits, and primates, which can be infrequently passed to humans, allowing the incidence of human-to-human transmission ^[16][27]. The Poxviridae family is divided into two taxonomic groups: Entomopoxvirinae and Chorodopoxvirinae. The subfamily classification depends upon whether the virus infects insects, as in Entemopovirinae, or vertebrates, as in Chorodopoxvirinae ^[17][28].

DNA viruses usually increase and express their genomes in the nucleus, making substantial use of cellular proteins; unfortunately, this is not the case for poxviruses ^[18][19][29,30]. The main portion of the genome will contain genes participating the important function, such as virus assembly and transcription, while some are located at termini which participate in virus–host interactions ^[20][31]. Poxviruses encode more than 150 genes, and 49 genes are common across all sequence members of the provirus family, while 90 are frequent inside the subfamily of chorodopoxviruses ^[21][32]. Further, poxvirus genera are divided into eight vertebrates: Yatapoxvirus, Orthopoxvirus, Caprioxviru, Molluscipoxvirus, Suipoxvirus, Capripoxvirus, Avpoxvirus, and Parapoxvirus (Figure 1). These viruses share the same DNA sequence with the same antigens for reactivity ^[22][33].

Poxviruses contain the human smallpox virus, declared eradicated in 1980 by the World Health Organization. Other poxviruses that can infect humans include the cowpox virus, smallpox virus, and Akhmeta virus, as well as viruses from different animal species that can cause a pandemic when combined with the monkeypox virus. The monkeypox virus is the most prevalent of these in humans. Bovine pox is another zoonotic disease with a large population in the animal kingdom, a clear relationship to livestock exposure in humans with variable prevalence and severity and a progression of several weeks. Paraboxvirus is a viral genus in the poxvirus family that includes species widespread among sheep, goats, cattle, camels, and the cervix. They are emollients in humans (breast nodules) infected by oral or pharyngeal (papular stomatitis) or skin contact (cellular dermatitis), typically with a moderate granulomatous reaction, causing a variety of clinical manifestations in animals.

Moreover, Paraboxvirus results in the formation of large nodular or vascular lesions. The species generates less immunity than Orthopoxviruses, increasing the likelihood of reinfection. Molluscum contagiosum is a common disease in humans, children, and adults caused by species of the genus Molluscipoxvirus, with specific human swellings and erythematous papules mimicking soft tumors, usually with few and variable numbers of immunizations. In the planting area, it is mainly distributed in roots, trunk, and limbs. Immunity is self-limited. The spreading of Molluscum contagiosum disease via direct contact with the genital lesions is facilitated by sexual contact and is also spread by Candida.

In contrast to other viruses, smallpox viruses have a much lower mutation ability than RNA viruses, such as influenza viruses. However, these viruses have extensive genetic ability, which explains their ability to attack and evade the virus and the immune system ^[23][24][34,35].

Poxvirus mature structure (Figure 2) has a distinctive dumbbell-shaped nucleoprotein core composed of a double-stranded DNA genome ^[6][17]. Monkeypox virions consist of 30 structural and membrane viral proteins, virus-encoded DNA-dependent RNA polymerase, and associated transcription enzymes ^[25][26][46,47]. The virus genome comprises 197,000 bp and contains hairpin termini along with >190 non-overlapping open reading frames (ORFs) ^[27][28][48,49]. The genome’s highly conserved central coding region is guarded by variable ends comprising inverted terminal repeats. At least ninety open reading frames (ORFs) are required for the virion’s replication and morphogenesis. Many non-essential ORFs play a role in the differences in poxvirus host tropism, immunomodulation, and pathogenesis, with many ORFs yet to be functionally categorized ^[29][50].

The pathogenicity and pathophysiology of the monkeypox virus begin with virus transmission, which starts with close contact of animal to human or human-to-human. Smallpox and monkeypox infect through the host’s respiratory or oropharyngeal mucosa. The virus enters through the inoculation site and begins replication in the respiratory and oropharyngeal mucosa. Viruses spread to the local lymph nodes in primary viremia. However, these viruses enter lymph nodes and organs via blood circulation in secondary viremia. This process represents the incubation period of 7 to 14 or 21 days ^[30][39].

External virion proteins, cellular glycosaminoglycans on the target cell’s surface, and extracellular matrix components are most likely involved in monkeypox virion attachment. Poxviruses enter host cells via a low-pH endosomal pathway or direct fusion with the plasma membrane at neutral pH, releasing the viral core in the cytoplasm. A complex of 12 non-glycosylated viral membrane proteins is required for intracellular mature virions and enveloped extracellular virions to fuse with the cell ^[31][51]. Following entry, the virus-encoded multi-subunit DNA-dependent RNA polymerase initiates viral transcription, followed by the translation of early, intermediate, and late proteins on host ribosomes ^[32][52]. Poxvirus DNA synthesis occurs in cytoplasmic structures known as “factories”, which gradually transition from compact DNA-containing structures wrapped in Endoplasmic reticulum membranes to crescent-shaped structures where virion assembly takes place. While most mature virions remain within the cell (intracellular mature virions), some are transported via microtubules and enveloped by two Endoplasmic reticulum or Golgi-derived membranes. These enveloped virions can either initiate actin polymerization, which propels the particle on an actin tail toward an adjacent cell, or exit the cell via cytoplasmic membrane fusion and become enveloped extracellular virions (Figure 3) ^[33][53].