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Species of double-stranded DNA virus
Monkeypox virus (MPV, MPXV, or hMPXV) is a species of double-stranded DNA virus that causes monkeypox in humans and other mammals. Monkeypox virus is a zoonotic virus belonging to the orthopoxvirus genus, making it closely related to the variola (VARV), cowpox (CPX), and vaccinia (VACV) viruses. MPV is oval-shaped with a lipoprotein outer membrane. The genome is approximately 190 kb.
The variola and monkeypox virus are both orthopoxviruses, and so the smallpox vaccine is effective against monkeypox if given within 35 years before contracting the disease.[1] The clinical presentation of Monkeypox is similar to smallpox, but with a milder rash and lower mortality rate.[2][3][4] The virus is transmissible between animals and humans, by direct contact to the lesions or bodily fluids.[5] Monkeypox was given its name after being isolated from monkeys, but the majority of the carriers of this virus are rodents.
Variation in virulence of the virus has been observed in isolates from Central Africa, where strains are more virulent than those from Western Africa.[2] The two areas have distinct clades of the virus, termed cladeI, formerly the Congo Basin (Central African) clade, and cladeII, formerly the West African clade.[6] Though there are many natural hosts for the monkeypox virus, the exact reservoirs and how the virus is circulated in nature needs to be studied further.
Though the monkeypox virus has been circulating around the globe for the past several decades, first discovered in 1970, research on this virus is minimal compared to other orthodox viruses. Most of the what is known about the monkeypox virus is information pieced together from studies on different but related viruses, notably other orthopox viruses.[7]
MPV is part of the genus Orthopoxvirus, belonging to the Poxviridae family, which have been listed by the WHO as diseases with epidemic or pandemic potential.[8] There are two major clades one from the Congo Basin and the other one has been endemic to the West Africa region. The Congo Basin clade has been found to be more virulent and deadly with a reproductive number of 0.6 to 1.0.[9]
MPV is 96.3% identical to the variola virus in regards to its coding region, but it does differ in parts of the genome which encode for virulence and host range.[10] Through phylogenetic analysis, it was found that MPV is not a direct descendent of the variola virus.[10]
The monkeypox virus, like other poxviruses, is oval shaped, with a lipoprotein outer membrane. The outer membrane protects the enzymes, DNA, and transcription factors of the virus.[11] Typical DNA viruses replicate and express their genome in the nuclease of ekaryotic cells. They heavily rely on the host cells machinery; however, the monkeypox viruses rely mostly on the protein encoded in their genome that allow them to replicate in the cytoplasm.[12]
Genome of the monkeypox virus is around 200kb long coding for approximately 200 proteins. It has double stranded DNA which presents in a linear shape with covalently closed hairpin ends; the 3 and 5 ends are not free.[13] Similar to other poxviruses, the irons of monkey pox have large oval shaped envelopes. Within each viiron there is a core which holds the genome along with the enzymes that assist in dissolving the protein coat and replication.[14] The center of the genome codes for genes involved in key functions such as viral transcription and assembly; genes located on the extermities of the viral genome are associated more towards interactions between the virus and the host cell such as spike protein characteristics.[12]
The monkeypox DNA genome consists of approximately 197 kb with 190 non-overlapping Open Reading Frames (ORFs).[15] The monkeypox virus contains a conserved coding region, with variable inverted terminal repeats at each end.[15]
As shown in the image below, the monkeypox virus is relatively large compared to other viruses. This makes it harder for the virus to breach the defenses of the host defenses, such as crossing past gap junctions. Furthermore, the large size makes it harder for the virus to quickly replicate and evade immune response.[12] To evade host immune systems, and buy more time for replication; the monkeypox and other orthopox viruses has evolved to evade host immune cells by coding for both intracellular and extracellular modulatory proteins.
The monkeypox virus has multiple surface proteins that facilitate its entry into host cells; the virus can use 11-12 transmembrane proteins to merge with the host cells. It likely binds to glycosaminoglycans or laminin on the cell surface.[16]Due to it being a DNA virus with a relatively low reproduction number, the virus is less likely to mutate compared to RNA viruses such as SARS-COV-2.[9]
As an Orthopoxvirus, MPV replication occurs entirely in the cell cytoplasm within 'factories'- created from the host rough endoplasmic reticulum (ER)- where viral mRNA transcription and translation also take place.[17][18] The factories are also where DNA replication, gene expression, and mature virions (MV) are created.[19]
MVs are able to bind to the cell surface with the help of viral proteins.[20] Virus entry into the host cell plasma membrane is dependent on a neutral pH, otherwise entry occurs via a low-pH dependent endocytic route.[20] The MV of the monkeypox virus has an Entry Fusion Complex (EFC), allowing it to enter the host cell after attachment.[20]
Translation of mRNA into structural virions occurs using the host ribosomes.[17] Gene expression begins when MPV releases viral proteins and enzymatic factors that disable the cell.[3] Mature virions are infectious, however, they will stay inside the cell, until they are transported from the factories to the Golgi/endosomal comportment.[19] Protein synthesis allows for the ER membrane of the factory to dismantle, while small two lipid bilayer membranes will appear to encapsulate the genomes of new virions, now extracellular viruses (EVs).[3][17][19] The VPS52 and VPS54 genes of the GARP complex, which is important for transport, are necessary for wrapping the virus, and formation of EVs.[19] DNA concatemers process the genomes, which appear in new virions, along with other enzymes, and genetic information needed for the replication cycle to occur.[3] EVs are necessary for the spread of the virus from cell-to-cell and its long-distance spread.[19]
The MPV virus is primarily transmitted through direct contact, infection from respiratory droplets is much lower. These two different modes of transmission also determines the host cells that are targeted by the MPV virus.
Zoonotic transmission can occur from direct contact with the blood, bodily fluids, wounds, or mucosal lesions of infected animals whether they are dead or alive. The virus is thought to have originated in Africa where evidence of the virus has been observed in multiple animals ranging from rope squirrels, tree squirrels, Gambian pouched rats, dormice, different species of monkeys. Though the natural reservoir of the monkeypox virus has not yet been established, rodents are speculated to be the most likely reservoir. Eating meat that has not been properly cooked and consuming other products of infected animals proves to be a major risk factor in the spread of infection.[21]
Anthropogenic spread of the monkey pox disease is attributed to close contact with respiratory secretions and skin lesions of infected people or contaminated surfaces. For the virus to propagate through inhalation of contaminated air droplets, prolonged face to face contact is required. Pregnant women can spread the virus to their fetus through the placenta.[22] In the United States, men are more disproportionately infected by the virus primarily during intercourse.[23] The effective reproduction number of monkeypox has been found to be the highest in the United States, estimated as 1.55 (95% CrI: 1.42, 1.73).[24] This means a single infected person is, on average, spreading it to 1.55 people.
The incubation period is between generally between 6 and 13 days; however, can range anywhere from 5 to 21 days.[21] Prodromal symptoms include swelling of lymph nodes, muscle pain, headache, fever, prior to the emergence of the rash.[25]
Signs and symptoms of monkeypox usually present themselves after the incubation period which can range from 521 days but is most commonly in the range of 613 days.[21] Being a self-limited virus, the symptoms of monkeypox in humans does not typically last longer than 4 weeks but can vary in severity depending on several factors including age of the patient and extent of time exposed to the virus. Children and immunocompromised patients are more likely to experience severe symptoms when exposed and infected with monkeypox. Monkeypox has many similar symptoms to other pox viruses in the infection period including fever, headaches, back pain, muscle pains and an intense lack of energy.[21] A sign unique to monkeypox compared to other pox viruses is lymphadenopathy, or swelling of the lymph nodes, particularly in the mandibular, cervical, or inguinal regions. Skin lesions typically present themselves on patients within 3 days of experiencing fever where they affect the face in an overwhelming majority of cases and other extremities of the body before affecting the trunk. The rash gradually develops on the body progressing from macules to pustules over a period of time eventually crusting over and falling off, sometimes sloughing off a portion of skin depending on the number of lesions and the severity of the case.[21]
Because of the close relation of monkeypox to other poxviruses such as smallpox, many of the same vaccines that have been proven to protect against smallpox are presumed to protect against the human monkeypox virus as well.[27] These presumptions about the effectiveness of smallpox vaccines for the use of treating the human monkeypox virus are not yet conclusive, as smallpox vaccinations have stopped being administered in many countries, like the United States, after the virus was deemed to have been eradicated.[27] Still, the CDC has made a recommendation for those considered at high risk for infection by the monkeypox virus to consider receiving a smallpox vaccine. There are three existing smallpox vaccines in the US Strategic National Stockpile, two of which, JYNNEOS and ACAM2000, are licensed for protection against smallpox.[27] The JYNNEOS vaccine is a two-dose vaccine that was developed to fight and protect against both the smallpox and monkeypox viruses, while the ACAM2000 is a vaccine that was developed to protect against smallpox but has been approved to help protect against monkeypox as well.[27] People who have had close contact with other humans or animals that were shown to have monkeypox are recommended to get vaccinated. Other prevention recommendations from the CDC are to avoid interacting with or touching materials that have been touched by an infected animal or human as well as to rinse your hands with soap and water following exposure or contact with an infected animal or human.
As a self-limited disease, the Monkeypox virus generally does not require treatment in the majority of people who acquire it.[21] In general, most patients infected by Monkeypox will recover within 24 weeks without treatment. While fatality rate associated with Monkeypox is significantly lower than other poxviruses like smallpox (~ 30%), the fatality rate associated with those infected by the Monkeypox virus is regionally variable and ranges from less than 1% to as high as 11%. Thus, treatment options are often necessary for individuals who are immunocompromised or have a higher risk for severe disease. Currently, there are no FDA-approved treatments for the Monkeypox virus specifically. There are, however, FDA-approved antivirals that are designed to treat smallpox and are thought to potentially be able to treat Monkeypox in humans as well. The treatment of choice for smallpox in humans is Tecovirimat (TPOXX). TPOXX has not been approved by the FDA for treatment against Monkeypox, but has been approved by the CDC to be used as a form of early treatment against non-variola orthopoxvirus infections, which includes Monkeypox, under an Investigational New Drug (EA-IND) protocol.
Pox viruses have mechanisms to evade the hosts' innate and adaptive immune systems. When infected human fibroblast cells have been observed to show cytopathic changes, but gene expression of the host cell remains unchanged. Interferon produced by human fibroblast cells were not sufficient to slow viral replication.[28] The Monkeypox virus gene BR-209 is an interleukin-1 (IL-1) inhibitor that prevents interaction with the receptor.[29] The viral complement control protein (CCP), also known as MOPICE, a virulence factor, allows the virus to evade neutralization, opsonization, viral particle lysis, and phagocytosis.[30]
The monkey pox virus can prevent apoptosis in infected cells by targeting apoptotic pathways; the mechanism is still under research.[31][29] Moreover, the monkey pox virus can evade cytotoxicity mediated by t-cell and natural killer cells by producing MHC classI-like protein(OMCP) which resembles MHC class I module and it binds to NKG2D. Natural killer T cells continually survey cells with NKG2D for absence of MHC class I proteins; the monkeypox virus with its OMCP passes the check.[29] The virus also produces other proteins that further block cytotoxic activities. Evading the host immune system is crucial because of how large the monkeypox virus is.
In short, MPV has a unique immune system, MHC dependent, evasion tactic to evade antiviral CD4+ and CD8+ T cell responses.[32]
The virus is subclassified into two main clades, the Central African/Congo Basin clade (CA) and the West African clade (WA).[8] The World Health Organization uses Roman numerals to denote each clade and a lowercase Latin script letter for subclades.[6]
At the protein level, the CA clade and WA clade share 170 orthologs, and their transcriptional regulatory sequences show no significant differences.[8] Both clades have 53 common virulence genes, which contain different types of amino acid changes. 121 of the amino acid changes in the virulence genes are silent, while 61 are conservative, and 93 are non-conservative.[8]
Both clades vary in virulence, with the CA clade having more human-human transmission, and having a higher mortality rate in non-vaccinated people.[8] The WA clade was thought to be less transmissible between humans.[8] The 2022 Monkeypox outbreak was caused by the WA clade of the virus.[33]
Endemic West African clade
Endemic Congo Basin clade
Both clades recorded
West African clade outbreak in 2022
Monkeypox virus is carried by various animals including primates.[37] It was first identified by Preben von Magnus in Copenhagen, Denmark, in 1958 in crab-eating macaque monkeys (Macaca fascicularis) being used as laboratory animals.[38] The 2003 outbreak in the United States was traced to prairie dogs infected from an imported Gambian pouched rat from Ghana.[39]
Monkeypox virus causes disease in both primates and in other animals. The virus is mainly found in tropical rainforest regions of Central and West Africa.[40]The virus is mainly found in the tropical forests of Central Africa and West Africa.[40] It was first discovered in monkeys in 1958, and in humans in 1970. Between 1970 and 1986, over 400 cases in humans were reported. Small viral outbreaks with secondary human-to-human infection occur routinely in equatorial Central and West Africa.[41] The primary route of infection is thought to be contact with the infected animals or their bodily fluids.[41] The first reported outbreak outside Africa occurred in 2003 in the Midwestern United States in Illinois, Indiana, and Wisconsin, with one occurrence in New Jersey. A significant outbreak in Nigeria occurred in 2017.[42]
The Monkeypox virus is a highly complex virus and is not yet fully understood. Many laboratories across the globe continue to study the virus as it has been spreading significantly outside of its endemic areas. Pathologic examination of the virus are carefully being done on formalin-fixed or inactivated tissues. One study done by Manes et al. inoculated a MPV strain obtained from the CDC into HeLa cells. The original strain was obtained from a victim of the virus.[43] Most of our current understanding of the monkeypox virus stems from the knowledge cultivated from studying the variola virus.
Moreover, there are multiple sites conducting epidemiological analysis on the spread of the disease and its evolution as new variants arise. Like the public extinction of smallpox through a global coordinated effort of vaccination, it may be possible to drive the monkeypox virus into extinction with effective vaccination due to its relatively low virulence.
The Tdap vaccine is a combination vaccine. It protects preteens and adults against three diseases: tetanus, diphtheria, and pertussis (whooping cough).
Tetanus and diphtheria are rare in the United States today, but whooping cough continues to spread.
Tdap stands for tetanus (T), diphtheria, (D), and acellular pertussis (aP). The Tdap vaccine became available in 2005 for older children and adults. Before 2005, there was no pertussis vaccine for anybody over 6 years of age.
Tdap is different than the DTaP vaccine (diphtheria, tetanus, and whooping cough), which is given to infants and children in five doses, starting at 2 months of age. Tdap is only for those above age 7.
Nope. Diphtheria, pertussis, and tetanus vaccines arent live vaccinations.
Types of vaccines that arent live include:
Since the Tdap vaccine isnt live, it cant cause these diseases.
Tetanus is not a communicable disease, meaning it doesnt pass from person to person. The bacteria are usually found in soil, dust, and manure and enter the body through breaks in the skin.
Tetanus is often referred to as lockjaw because tightening of the jaw muscles is one of the most common signs of this infection.
Tetanus can lead to serious health problems, including an inability to open your mouth and difficulty swallowing and breathing.
Today, tetanus is uncommon in the United States, with an average of about 30 reported cases each year.
Diphtheria is caused by strains of bacteria that are typically transmitted through respiratory droplets, coughing, or sneezing.
People can also contract diphtheria from contact with open sores or ulcers containing the bacteria.
The bacteria typically affect the respiratory system, which can cause:
Diphtheria can lead to difficulty breathing, heart failure, paralysis, and even death.
The Tdap vaccine protects against whooping cough, which can be debilitating and last for months. It can cause uncontrollable, violent coughing that makes it hard to breathe or consume food or drinks.
Tdap also helps protect infants who are too young to be vaccinated against whooping cough. Parents, siblings, and grandparents are often the source of whooping cough in infants.
Young children have been vaccinated against whooping cough since the 1940s. But protection against the disease naturally wears off over time, so booster vaccines can help keep up immunity. To stay up to date, contact a healthcare professional to set up routine reviews of vaccine history for you and your child.
Every vaccine comes with a chance of side effects, and the Tdap vaccine is no exception. Fortunately, reported side effects with Tdap are generally mild and go away on their own.
Mild to moderate side effects may include:
Severe problems after the Tdap vaccine are rarely reported, but may include:
If you notice any of these severe symptoms after receiving the Tdap vaccine, seek medical attention.
The cost of the vaccine is covered under most private insurance plans. Be sure to check with your insurance provider for details. You can also check with your state health departments or local health centers for low-cost or free vaccinations.
Tdap vaccines are also covered under Medicare part D plans. There may be a cost associated with your specific plan, though, so check with your Medicare representative.
Vaccines for Children is a federally funded program that provides vaccines for children 18 years and younger who are uninsured, underinsured, Medicaid-eligible, American Indian, or Alaska Native.
The Centers for Disease Control and Prevention (CDC) recommends that those who are pregnant receive a Tdap vaccine anytime between weeks 27 and 36 of pregnancy.
If youre pregnant, once you have protection from the vaccine, whooping cough is less likely to transmit to a newborn. Infants are more likely to develop severe, life threatening complications from whooping cough.
Doctors will recommend a Tdap vaccination schedule depending on your age and vaccination history:
If youre age 18 or older, the CDC recommends that you get a dose of Tdap in place of your next Td (tetanus and diphtheria) booster if:
A Td booster is usually given every 10 years with a single injection in the upper arm.
You should get a Tdap booster before the 10-year interval if:
Although the risk of having a severe allergic reaction to a Tdap vaccine is very low, certain people should avoid getting the Tdap vaccine, including:
Talk with your doctor if you have seizures or another condition that affects the nervous system.
Also, let your doctor know if youve ever had Guillain-Barr syndrome or if youve ever experienced severe pain or swelling after any previous vaccine containing diphtheria, tetanus, or pertussis.
A healthcare professionals office such as a pediatrician, family practitioner, or community health clinic is usually the best place to receive a Tdap vaccine.
These vaccines may also be available for adults at:
You can also reach out to federally funded health centers as well as your state health department to learn where to get a vaccine near you.
Getting a Tdap vaccine is an important part of maintaining your health as well as the health of infants. Reach out to your healthcare professional on a regular basis to make sure that your Tdap vaccinations are up to date.
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