Herpes simplex virus: Difference between revisions
No edit summary |
No edit summary |
||
| Line 18: | Line 18: | ||
}} | }} | ||
It's the first human herpes virus to be discovered. The word herpes is derived from a Greek verb meaning to creep. Herpes simplex is actually a genus comprising two types of herpes viruses: HSV-1 and HSV-2. Both have similar structures, antigenic determinants, but cause infections in different parts of the body. HSV-1 is usually transmitted through saliva and causes oropharyngeal infections. HSV-2 is transmitted sexually or from mother to newborn at birth. Another characteristic of this group is that these viruses can lie in a latent phase, in which the virus does not multiply and remains in the dorsal root ganglia. During reactivation, the virus travels through sensory nerves from the ganglia back to the site of primary infection, where it again causes disease. | It's the first human [[herpes virus]] to be discovered. The word herpes is derived from a Greek verb meaning to creep. Herpes simplex is actually a genus comprising two types of herpes viruses: '''HSV-1 and HSV-2'''. Both have similar structures, antigenic determinants, but cause infections in different parts of the body. HSV-1 is usually transmitted through saliva and causes oropharyngeal infections. HSV-2 is transmitted sexually or from mother to newborn at birth. Another characteristic of this group is that these viruses can lie in a '''latent phase''', in which the virus does not multiply and remains in the dorsal root ganglia. During reactivation, the virus travels through sensory nerves from the ganglia back to the site of '''primary infection''', where it again causes disease. | ||
== Structure == | == Structure == | ||
Characteristic morphological features are typical of this group. These viruses contain in their capsid envelope a linear double-stranded DNA molecule of 125 to 248 kbp. The genes encode approximately 80 proteins. However, only 40 of these are involved in virus replication. The rest interact with the host cell and the immune system. The HSV genome encodes DNA-dependent DNA polymerase, deoxyribonuclease, thymidine kinase, ribonucleotide reductase and protease. The DNA is surrounded by a capsid consisting of 162 hollow hexagonal and pentagonal capsomeres. | Characteristic morphological features are typical of this group. These viruses contain in their capsid envelope '''a linear double-stranded [[DNA]] molecule''' of 125 to 248 kbp<ref name=":0">GREENWOOD, David. ''Medical microbiology : a guide to microbial infections. ''17. vydání. Edinburgh ; New York : Churchill Livingstone/Elsevier, 2007. <nowiki>ISBN 978-0-443-10210-3</nowiki>.</ref>. The genes encode approximately '''80 proteins'''<ref>MURRAY, Patrick R a Ken S ROSENTHAL. ''Medical microbiology. ''5. vydání. Philadelphia : Elsevier Mosby, 2005. <nowiki>ISBN 0-323-03303-2</nowiki>.</ref>'''.''' However, only 40 of these are involved in virus replication. The rest interact with the host cell and the immune system. The HSV genome encodes DNA-dependent DNA polymerase, deoxyribonuclease, thymidine kinase, ribonucleotide reductase and protease. The DNA is surrounded by a capsid consisting of 162 hollow hexagonal and pentagonal capsomeres.<ref name=":0" /> | ||
When the viral particle is mature, the capsid is surrounded by a lipid envelope that originates from the nucleus of the host cell. Glycoproteins that are encoded by the virus itself protrude from the lipid envelope. Glycoproteins gB and gD serve to capture and enter the potential host cell. Glycoprotein gH then allows the virion to be released within the cell. | When the viral particle is mature, the capsid is surrounded by a lipid envelope that originates from the nucleus of the host cell. '''[[Glycoproteins]]''' that are encoded by the virus itself protrude from the lipid envelope. '''Glycoproteins gB and gD''' serve to capture and enter the potential host cell. '''Glycoprotein gH''' then allows the virion to be released within the cell. | ||
== Replication == | == Replication == | ||
HSV can infect most cells in the human body. The virus attaches to the cell and fuses with the cell membrane. Its virion then enters the cytoplasm and travels to the nucleus. First, so-called DNA-binding proteins are transcribed, which stimulate DNA synthesis and which initiate the transcription of early viral genes. Early proteins include DNA-dependent DNA polymerase and thymidine kinase. Other viral proteins then suppress the production and even initiate the degradation of cellular mRNA and DNA. Viral glycoproteins originate in the Golgi apparatus and are incorporated into the cell membrane. New mature viral particles leave the host cell by exocytosis, intercellular junctions between cells or during host cell lysis. Infected cells usually do not survive such an attack and undergo necrosis. | HSV can '''infect most cells''' in the human body. The virus attaches to the cell and fuses with the cell membrane. Its virion then enters the cytoplasm and travels to the nucleus. First, so-called '''DNA-binding proteins''' are transcribed, which stimulate DNA synthesis and which initiate the transcription of early viral genes. Early proteins include DNA-dependent DNA polymerase and thymidine kinase. Other viral proteins then suppress the production and even '''initiate the degradation of cellular [[RNA - types, structure and function|mRNA]] and [[DNA - structure and function|DNA]]'''. Viral glycoproteins originate in the [[Golgi apparatus]] and are incorporated into the cell membrane. New mature viral particles leave the host cell by exocytosis, intercellular junctions between cells or during host cell lysis. Infected cells usually do not survive such an attack and undergo [[necrosis]]. | ||
== Diseases == | == Diseases == | ||
HSV-1 and HSV-2 are common human pathogens that cause painful and recurrent disease. Most of the time the course of the disease is mild, but this is not always the case. The manifestation varies and depends on many factors, the most important of which is the state of the immune system. The infection may present in a milder form as herpes labialis or herpes genitalis, or as life-threatening herpetic encephalitis. Care should be taken with ongoing infections in children and in immunosuppressed patients. In them, infections of the eye or brain can cause serious complications and even death. There is currently no effective vaccine to prevent HSV-1 or HSV-2 infection. | [[File:Herpes(PHIL 1573 lores).jpg|thumb|Infection in the lip area]] | ||
HSV-1 and HSV-2 are common human pathogens that cause '''painful and recurrent disease'''. Most of the time the course of the disease is mild, but this is not always the case. The manifestation varies and depends on many factors, the most important of which is the '''state of the immune system'''. The infection may present in a milder form as herpes labialis or herpes genitalis, or as life-threatening '''herpetic encephalitis'''. Care should be taken with ongoing infections in children and in immunosuppressed patients. In them, infections of the eye or brain can cause serious complications and even death. There is currently '''no effective vaccine to prevent HSV-1 or HSV-2 infection'''. | |||
The virus may be the causative agent: | |||
* skin infections, | * skin infections, | ||
* infections in the lip area, | * infections in the lip area, | ||
* eye infections, | * eye infections, | ||
* CNS infections - encephalitis and meningitis, | * CNS infections - [[encephalitis]] and [[meningitis]], | ||
* genital infections, | * genital infections, | ||
* neonatal infections. | * [[neonatal infections]]. | ||
=== Skin infections === | === Skin infections === | ||
Infections in the hand area are quite common. If they appear, then they are white in color, painful, but do not form typical sores. They are often associated with lymphatitis. Eczema herpeticum is a serious form. The disease resembles chickenpox. Extensive ulceration occurs due to protein loss and dehydration. The spread of the disease has fatal consequences. | Infections in the hand area are quite common. If they appear, then they are white in color, painful, but do not form typical sores. They are often associated with lymphatitis. '''''Eczema herpeticum''''' is a serious form. The disease resembles [[chickenpox]]. Extensive ulceration occurs due to protein loss and dehydration. The spread of the disease has fatal consequences. | ||
=== Infections in the mouth area === | === Infections in the mouth area === | ||
They are caused by both HSV-1 and HSV-2. Commonly, the infection manifests itself as acute, febrile gingivostomatitis in preschoolers. Fluid-filled boils occur fairly quickly around the lips and adjacent area. Children heal within 7-10 days. In older patients, this disease often occurs together with mononucleosis, often during pregnancy, in newborn babies or immunosuppressed patients. | They are caused by both '''HSV-1 and HSV-2'''. Commonly, the infection manifests itself as '''acute, febrile gingivostomatitis''' in preschoolers. Fluid-filled boils occur fairly quickly around the lips and adjacent area. Children heal within 7-10 days. In older patients, this disease often occurs together with [[mononucleosis]], often during pregnancy, in newborn babies or immunosuppressed patients. | ||
=== Eye infections === | === Eye infections === | ||
These are mainly caused by HSV-1, which can be transmitted to the eye manually during a cold or during a primary infection in childhood. It may present as conjunctivitis or keratoconjunctivitis with corneal ulcerations. Recurrent ocular infection may progress to epithelial keratitis, which is characterised by reduced corneal sensitivity. Disease caused by HSV tends to recur, especially in patients over 50 years of age. | [[File:Herpes simplex Lid.jpg|thumb|Infections in the eye area]] | ||
These are mainly caused by HSV-1, which can be transmitted to the eye manually during a cold or during a primary infection in childhood. It may present as '''[[conjunctivitis]] or keratoconjunctivitis''' with corneal ulcerations. Recurrent ocular infection may progress to epithelial keratitis, which is characterised by reduced corneal sensitivity. Disease caused by HSV tends to recur, especially in patients over 50 years of age.<ref name=":0" /> | |||
Untreated infections can lead to loss of vision. | Untreated infections can lead to '''loss of vision'''. | ||
=== CNS infections === | === CNS infections === | ||
HSV-2 infection manifests as serous meningitis. It is most commonly encountered in neonates of mothers with acute seeding of vesicles, after passage through the birth canal. The clinical picture is identical to other viral meningitis. | '''HSV-2''' infection manifests as '''serous meningitis'''. It is most commonly encountered in neonates of mothers with acute seeding of vesicles, after passage through the birth canal. The clinical picture is identical to other [[viral meningitis]]. | ||
HSV-1 causes acute haemorrhagic-necrotizing encephalitis with a severe course and very poor prognosis (lethality 30%, up to 70% in untreated patients). Approximately 30% of cases of HSV-induced encephalitis occur in patients under 20 years of age, and 50% of cases occur in patients over 50 years of age. It spreads retrograde from the ganglia n. trigeminus, most commonly affecting the frontotemporal region of the brain. | '''HSV-1''' causes '''acute haemorrhagic-necrotizing encephalitis''' with a severe course and very poor prognosis (lethality 30%, up to 70% in untreated patients). Approximately 30% of cases of HSV-induced encephalitis occur in patients under 20 years of age, and 50% of cases occur in patients over 50 years of age<ref name=":1">GOERING, Richard V a Hazel M DOCKRELL. ''Mimsova lékařská mikrobiologie. ''5. vydání. Praha : Triton, 2016. 568 s. <nowiki>ISBN 978-80-7387-928-0</nowiki>.</ref>. It spreads retrograde from the ganglia ''n. trigeminus'', most commonly affecting the frontotemporal region of the brain. | ||
It starts as a non-specific headache with increased temperature, progresses to seizures along with qualitative and quantitative impairment of consciousness. Hallucinations, behavioural and memory disturbances, aphasia and signs of cerebral oedema are common. Even with early treatment, permanent sequelae (most commonly memory impairment) often occur.{{Podrobnosti|Encefalitida způsobená herpes simplex viry}} | It starts as a non-specific headache with increased temperature, progresses to seizures along with qualitative and quantitative impairment of consciousness. Hallucinations, behavioural and memory disturbances, aphasia and signs of cerebral oedema are common. Even with early treatment, permanent sequelae (most commonly memory impairment) often occur.{{Podrobnosti|Encefalitida způsobená herpes simplex viry}} | ||
=== Genital infections === | === Genital infections === | ||
Both HSV-1 and HSV-2 can cause infection in the genital area. These infections are most common in sexually active individuals. Women have a more severe course than men. The incubation period is approximately 2-20 days. The infection is accompanied by fever and | [[File:GenitalGerpes.gif|thumb|Genital herpes]] | ||
Both HSV-1 and HSV-2 can cause infection in the genital area. These infections are most common in '''sexually active individuals'''. Women have a more severe course than men. The incubation period is approximately 2-20 days. The infection is accompanied by '''fever and malaise, urethritis and vaginal discharge'''. Local lymph nodes are enlarged. Local symptoms resolve after approximately 2 weeks. However, the virus latently infects the nerve endings, may reactivate and travel back along the nerves to the original site, where it causes '''recurrent genital herpes'''. Secondary '''mycotic or bacterial infections''' are also common. Complete cure may take several weeks for untreated infection. '''Aseptic meningitis''' may also develop in more than 10% of those affected by primoinfection.<ref name="Bartošová"> | |||
{{Citace | {{Citace | ||
| typ = článek | | typ = článek | ||
| Line 69: | Line 72: | ||
| ročník = 12 | | ročník = 12 | ||
| strany = 586-588 | | strany = 586-588 | ||
| issn = 1803-5256 }}</ref> | | issn = 1803-5256 }} | ||
</ref> | |||
=== Neonatal infections === | === Neonatal infections === | ||
They are relatively rare, but very dangerous. More than 60% of infected newborns suffer severe damage to the body. Infection is most commonly caused by HSV-2, which affects the newborn as it passes through the birth canal. The disease may or may not present with a skin rash. In most cases, a generalized infection becomes apparent around day 5 of postnatal life. Once the virus begins to spread, it causes fever, lack of appetite, irritability and sepsis. Pneumonia or jaundice may occur. Progressive liver failure with coagulopathy leads to death of the newborn around day 16. It is necessary to intervene fairly quickly with antiviral therapy and to monitor the newborn for the occurrence of a rash. Parenteral administration of acyclovir every 8 hours to newborns can reduce mortality to 29% for disseminated infection and 4% for CNS infection.{{Podrobnosti|Adnátní HSV infekce}} | They are relatively rare, but '''very dangerous'''. More than 60% of infected newborns suffer severe damage to the body. Infection is '''most commonly caused by HSV-2''', which affects the newborn as it passes through the birth canal. The disease may or may not present with a skin rash. In most cases, a generalized infection becomes apparent around '''day 5 of postnatal life'''. Once the virus begins to spread, it causes '''fever, lack of appetite, irritability and sepsis'''. '''Pneumonia or jaundice''' may occur. Progressive liver failure with [[coagulopathy]] leads to death of the newborn around day 16. It is necessary to intervene fairly quickly with antiviral therapy and to monitor the newborn for the occurrence of a rash. Parenteral administration of acyclovir every 8 hours to newborns can '''reduce mortality''' to 29% for disseminated infection and 4% for CNS infection.{{Podrobnosti|Adnátní HSV infekce}} | ||
== Diagnosis and treatment == | == Diagnosis and treatment == | ||
The presence of DNA of the virus can be demonstrated in fluid from blisters, saliva, conjunctival sacs, liquor. Cultures on tissue structures are gradually being replaced by molecular methods, where we can distinguish HSV-1 from HSV-2. Acyclovir, valacyclovir and famciclovir are used for the treatment of severe and early infections. If the patient is in serious condition, we can also administer acyclovir intravenously. Repeated attacks are difficult to treat, patients should take prophylactic antivirals at prodromal symptoms.<noinclude> | The presence of DNA of the virus can be demonstrated in fluid from blisters, [[saliva]], conjunctival sacs, liquor. Cultures on tissue structures are gradually being replaced by molecular methods, where we can distinguish HSV-1 from HSV-2. '''Acyclovir, valacyclovir and famciclovir''' are used for the treatment of severe and early infections. If the patient is in serious condition, we can also administer acyclovir intravenously. Repeated attacks are difficult to treat, patients should take prophylactic '''antivirals at prodromal symptoms'''.<ref name=":1" /><noinclude> | ||
== | == References == | ||
=== Related articles === | === Related articles === | ||
* Herpesviruses | * [[Herpesviruses]] | ||
* Herpes zoster | * [[Herpes zoster]] | ||
* Varicella-zoster virus | * [[Varicella-zoster virus]] | ||
* Encephalitis caused by herpes simplex viruses | * [[Encephalitis caused by herpes simplex viruses]] | ||
* Adenatal HSV infection | * [[Adenatal HSV infection]] | ||
* Viral meningitis | * [[Viral meningitis]] | ||
* Gingivostomatitis herpetica | * [[Gingivostomatitis herpetica]] | ||
* Antivirals | * [[Antivirals]] | ||
=== External links === | === External links === | ||
Revision as of 14:20, 2 February 2022
It's the first human herpes virus to be discovered. The word herpes is derived from a Greek verb meaning to creep. Herpes simplex is actually a genus comprising two types of herpes viruses: HSV-1 and HSV-2. Both have similar structures, antigenic determinants, but cause infections in different parts of the body. HSV-1 is usually transmitted through saliva and causes oropharyngeal infections. HSV-2 is transmitted sexually or from mother to newborn at birth. Another characteristic of this group is that these viruses can lie in a latent phase, in which the virus does not multiply and remains in the dorsal root ganglia. During reactivation, the virus travels through sensory nerves from the ganglia back to the site of primary infection, where it again causes disease.
Structure
Characteristic morphological features are typical of this group. These viruses contain in their capsid envelope a linear double-stranded DNA molecule of 125 to 248 kbp[1]. The genes encode approximately 80 proteins[2]. However, only 40 of these are involved in virus replication. The rest interact with the host cell and the immune system. The HSV genome encodes DNA-dependent DNA polymerase, deoxyribonuclease, thymidine kinase, ribonucleotide reductase and protease. The DNA is surrounded by a capsid consisting of 162 hollow hexagonal and pentagonal capsomeres.[1]
When the viral particle is mature, the capsid is surrounded by a lipid envelope that originates from the nucleus of the host cell. Glycoproteins that are encoded by the virus itself protrude from the lipid envelope. Glycoproteins gB and gD serve to capture and enter the potential host cell. Glycoprotein gH then allows the virion to be released within the cell.
Replication
HSV can infect most cells in the human body. The virus attaches to the cell and fuses with the cell membrane. Its virion then enters the cytoplasm and travels to the nucleus. First, so-called DNA-binding proteins are transcribed, which stimulate DNA synthesis and which initiate the transcription of early viral genes. Early proteins include DNA-dependent DNA polymerase and thymidine kinase. Other viral proteins then suppress the production and even initiate the degradation of cellular mRNA and DNA. Viral glycoproteins originate in the Golgi apparatus and are incorporated into the cell membrane. New mature viral particles leave the host cell by exocytosis, intercellular junctions between cells or during host cell lysis. Infected cells usually do not survive such an attack and undergo necrosis.
Diseases
.jpg)
HSV-1 and HSV-2 are common human pathogens that cause painful and recurrent disease. Most of the time the course of the disease is mild, but this is not always the case. The manifestation varies and depends on many factors, the most important of which is the state of the immune system. The infection may present in a milder form as herpes labialis or herpes genitalis, or as life-threatening herpetic encephalitis. Care should be taken with ongoing infections in children and in immunosuppressed patients. In them, infections of the eye or brain can cause serious complications and even death. There is currently no effective vaccine to prevent HSV-1 or HSV-2 infection.
The virus may be the causative agent:
- skin infections,
- infections in the lip area,
- eye infections,
- CNS infections - encephalitis and meningitis,
- genital infections,
- neonatal infections.
Skin infections
Infections in the hand area are quite common. If they appear, then they are white in color, painful, but do not form typical sores. They are often associated with lymphatitis. Eczema herpeticum is a serious form. The disease resembles chickenpox. Extensive ulceration occurs due to protein loss and dehydration. The spread of the disease has fatal consequences.
Infections in the mouth area
They are caused by both HSV-1 and HSV-2. Commonly, the infection manifests itself as acute, febrile gingivostomatitis in preschoolers. Fluid-filled boils occur fairly quickly around the lips and adjacent area. Children heal within 7-10 days. In older patients, this disease often occurs together with mononucleosis, often during pregnancy, in newborn babies or immunosuppressed patients.
Eye infections
These are mainly caused by HSV-1, which can be transmitted to the eye manually during a cold or during a primary infection in childhood. It may present as conjunctivitis or keratoconjunctivitis with corneal ulcerations. Recurrent ocular infection may progress to epithelial keratitis, which is characterised by reduced corneal sensitivity. Disease caused by HSV tends to recur, especially in patients over 50 years of age.[1]
Untreated infections can lead to loss of vision.
CNS infections
HSV-2 infection manifests as serous meningitis. It is most commonly encountered in neonates of mothers with acute seeding of vesicles, after passage through the birth canal. The clinical picture is identical to other viral meningitis.
HSV-1 causes acute haemorrhagic-necrotizing encephalitis with a severe course and very poor prognosis (lethality 30%, up to 70% in untreated patients). Approximately 30% of cases of HSV-induced encephalitis occur in patients under 20 years of age, and 50% of cases occur in patients over 50 years of age[3]. It spreads retrograde from the ganglia n. trigeminus, most commonly affecting the frontotemporal region of the brain.
It starts as a non-specific headache with increased temperature, progresses to seizures along with qualitative and quantitative impairment of consciousness. Hallucinations, behavioural and memory disturbances, aphasia and signs of cerebral oedema are common. Even with early treatment, permanent sequelae (most commonly memory impairment) often occur. Iron
Genital infections
Both HSV-1 and HSV-2 can cause infection in the genital area. These infections are most common in sexually active individuals. Women have a more severe course than men. The incubation period is approximately 2-20 days. The infection is accompanied by fever and malaise, urethritis and vaginal discharge. Local lymph nodes are enlarged. Local symptoms resolve after approximately 2 weeks. However, the virus latently infects the nerve endings, may reactivate and travel back along the nerves to the original site, where it causes recurrent genital herpes. Secondary mycotic or bacterial infections are also common. Complete cure may take several weeks for untreated infection. Aseptic meningitis may also develop in more than 10% of those affected by primoinfection.[4]
Neonatal infections
They are relatively rare, but very dangerous. More than 60% of infected newborns suffer severe damage to the body. Infection is most commonly caused by HSV-2, which affects the newborn as it passes through the birth canal. The disease may or may not present with a skin rash. In most cases, a generalized infection becomes apparent around day 5 of postnatal life. Once the virus begins to spread, it causes fever, lack of appetite, irritability and sepsis. Pneumonia or jaundice may occur. Progressive liver failure with coagulopathy leads to death of the newborn around day 16. It is necessary to intervene fairly quickly with antiviral therapy and to monitor the newborn for the occurrence of a rash. Parenteral administration of acyclovir every 8 hours to newborns can reduce mortality to 29% for disseminated infection and 4% for CNS infection. Iron
Diagnosis and treatment
The presence of DNA of the virus can be demonstrated in fluid from blisters, saliva, conjunctival sacs, liquor. Cultures on tissue structures are gradually being replaced by molecular methods, where we can distinguish HSV-1 from HSV-2. Acyclovir, valacyclovir and famciclovir are used for the treatment of severe and early infections. If the patient is in serious condition, we can also administer acyclovir intravenously. Repeated attacks are difficult to treat, patients should take prophylactic antivirals at prodromal symptoms.[3]
References
Related articles
- Herpesviruses
- Herpes zoster
- Varicella-zoster virus
- Encephalitis caused by herpes simplex viruses
- Adenatal HSV infection
- Viral meningitis
- Gingivostomatitis herpetica
- Antivirals
External links
References
- ↑ a b c GREENWOOD, David. Medical microbiology : a guide to microbial infections. 17. vydání. Edinburgh ; New York : Churchill Livingstone/Elsevier, 2007. ISBN 978-0-443-10210-3.
- ↑ MURRAY, Patrick R a Ken S ROSENTHAL. Medical microbiology. 5. vydání. Philadelphia : Elsevier Mosby, 2005. ISBN 0-323-03303-2.
- ↑ a b GOERING, Richard V a Hazel M DOCKRELL. Mimsova lékařská mikrobiologie. 5. vydání. Praha : Triton, 2016. 568 s. ISBN 978-80-7387-928-0.
- ↑
Kategorie:Mikrobiologie Kategorie:Viry Kategorie:Infekční lékařství Kategorie:Dermatovenerologie Kategorie:Pediatrie Kategorie:Gynekologie Kategorie:Neurologie
