Wikipedia

Lymphocytic choriomeningitis

(Redirected from Lymphocytic meningitis)

Lymphocytic choriomeningitis (LCM) is a rodent-borne viral infectious disease that presents as aseptic meningitis, encephalitis or meningoencephalitis. Its causative agent is lymphocytic choriomeningitis mammarenavirus (LCMV), a member of the family Arenaviridae. The name was coined by Charles Armstrong in 1934.[2]

Lymphocytic choriomeningitis
Other namesBenign lymphocytic meningitis, lymphocytic meningoencephalitis, serous lymphocytic meningitis, la maladie d'Armstrong[1]
SpecialtyInfectious disease

Lymphocytic choriomeningitis (LCM) is "a viral infection of the membranes surrounding the brain and spinal cord and of the cerebrospinal fluid".[3] The name is based on the tendency of an individual to have abnormally high levels of lymphocytes during infection. Choriomeningitis is "cerebral meningitis in which there is marked cellular infiltration of the meninges, often with a lymphocytic infiltration of the choroid plexuses".[4]

Signs and symptoms

edit

LCMV infection manifests itself in a wide range of clinical symptoms, and may even be asymptomatic for immunocompetent individuals.[5] Onset typically occurs between one or two weeks after exposure to the virus and is followed by a biphasic febrile illness. During the initial or prodromal phase, which may last up to a week, common symptoms include fever, lack of appetite, headache, muscle aches, malaise, nausea, and/or vomiting. Less frequent symptoms include a sore throat and cough, as well as joint, chest, and parotid pain. The onset of the second phase occurs several days after recovery, and consists of symptoms of meningitis or encephalitis. Pathological findings during the first stage consist of leukopenia and thrombocytopenia. During the second phase, typical findings include elevated protein levels, increased leukocyte count, or a decrease in glucose levels of the cerebrospinal fluid).[6]

Occasionally, a patient improves for a few days, then relapses with aseptic meningitis, or very rarely, meningoencephalitis.[7] Patients with meningitis may have a stiff neck, fever, headache, myalgia, nausea and malaise. In some occasions, meningitis occurs without a prodromal syndrome.[7] Meningoencephalitis is characterized by more profound neurological signs such as confusion, drowsiness, sensory abnormalities and motor signs. Underreported complications include myelitis, Guillain–Barré-type syndrome, cranial nerve palsies, transient or permanent hydrocephalus, sensorineural hearing loss, orchitis, arthritis and parotitis.[7] LCMV infections have also been associated with pancreatitis, pneumonitis, myocarditis and pericarditis.[7] The entire illness usually lasts 1 to 3 weeks;[7] nonetheless, temporary or permanent neurological damage is possible in all central nervous system infections, especially in cases of meningoencephalitis. Chronic infections have not been reported in humans and deaths rarely occur.[7]

Cause

edit

Virus biology

edit
Lymphocytic choriomeningitis mammarenavirus
 
Negative stain electron micrograph of an arenavirus from a mouse that tested positive for LCM
Virus classification  
(unranked): Virus
Realm: Riboviria
Kingdom: Orthornavirae
Phylum: Negarnaviricota
Class: Ellioviricetes
Order: Bunyavirales
Family: Arenaviridae
Genus: Mammarenavirus
Species:
Lymphocytic choriomeningitis mammarenavirus
Synonyms
  • Lymphocytic choriomeningitis virus

There are several strains of LCM virus, among which the most widely used are LCMV Armstrong and LCMV Clone 13. Armstrong is the original virus strain which was isolated from the brain by Charles Armstrong in 1934. It triggers a vigorous cytotoxic T lymphocytes (CTL) response and thus, it is cleared rapidly by the host. This is referred to as acute (Armstrong) LCMV infection.[8] On the other hand, Clone 13 is a variant of the Armstrong viral strain, isolated from the spleen and is consequently tropic for visceral organs. It was first isolated from mice which sustained a persistent LCMV infection from birth.[8] This variant potentiates a less vigorous CTL response in the immune system, and thus can ultimately persist in the host organism indefinitely. The latter is referred to as chronic (Clone 13) LCMV infection.[8]

LCMV is a spherical enveloped virus with a diameter between 60 and 300 nm.[9] The helical nucleocapsid contains an RNA genome consisting of two negative single-stranded RNA segments.[9] The negative RNA strand, complementary to the necessary mRNA strand, indicates that it must first be transcribed into a positive mRNA strand before it can be translated into the required proteins. The L strand is ambisense RNA, encoding multiple proteins in opposite directions, separated by an intergenic region. It is approximately 7.2 kb in size and encodes a high-molecular-mass protein (L; 200 kDa) and an 11 kDa small polypeptide Z with unknown function and a ring finger motif.[9] The viral RNA-dependent RNA polymerase is encoded by the L protein which contains conserved characteristic motifs throughout all the RNA-dependent, RNA-polymerases. The S strand is ambisense and approximately 3.4 kb in size.[9] It encodes the two main structural proteins: nucleo-protein (NP) (63 kDa) and glycoprotein precursor complex (GPC) (75 kDa).[10] The latter undergoes posttranslational cleavage at two separate steps: first in the endoplasmic reticulum, where following translation on the membrane, the stable signal peptide region is cleaved by signal peptidase (SPase); notably, this signal peptide is retained, in contrast to other viruses. The second cleavage occurs at the Golgi apparatus, where GP1-GP2, having been trafficked to the Golgi, is cleaved into separate mature viral glycoproteins, GP1 and GP2 (with cleavage mediated by SK1-/PS1 or MBTPS1).[9] The spikes present on the virion envelope are dictated by tetramer formation of GP-1 and GP-2.[9]

When LCMV attacks a cell, the process of replication starts by attachment of the virus to host receptors through its surface glycoproteins.[11] It is then endocytosed into a vesicle inside the host cell and creates a fusion of the virus and vesicle membranes. The ribonucleocapsid is then released in the cytoplasm. The RNA-dependent, RNA-polymerase[11] brought along with the virus initially binds to a promoter on the L and S segments and begins transcription from negative-stranded to a positive-stranded mRNA. The formation of a strong hairpin sequence at the end of each gene terminates transcription.[11] The mRNA strands are capped by the RNA-dependent, RNA-polymerase in the cytoplasm[11] and are then subsequently translated into the four proteins essential for LCMV assembly. The ribonucleocapsid interacts with the Z matrix protein[11] and buds on the cell membrane, releasing the virion out from the infected cell.

The first arenavirus, Lymphocytic choriomeningitis mammarenavirus (LCMV), was isolated in 1933 by Charles Armstrong during a study of an epidemic in St. Louis. Although not the cause of the outbreak, LCMV was found to be a cause of nonbacterial or aseptic meningitis.[citation needed]

In 1996, Peter Doherty and Rolf Zinkernagel shared the Nobel Prize in Medicine and Physiology,[8] for their work with LCMV which led to a fundamental understanding of the adaptive immune response, MHC restriction. In the 1970s, studies concerning the importance of MHC locus were done exclusively in transplantation and tumor rejection. Taking this into consideration, Doherty and Zinkernagel were working on the response of mice to virus infections. They observed that T-cell receptors must recognise a complex of foreign antigen and an MHC antigen in order to destroy infected cells. Their key experiment involved harvesting of splenocytes containing LCMV-specific cytotoxic T lymphocytes (CTL) from an infected mouse strain A.[8] These were then mixed in vitro with virus infected fibroblasts or macrophages from two different mouse strains, A and B. By the method of Cr-release cytotoxicity assay,[8] thereby tagging the CTL with chromium-51 (Cr-51), the CTL destruction of infected cells was quantified by release of Cr-51. The results showed that CTL killed only the infected cells from strain A, and they did not lyse uninfected cells or infected cells from strain B.[8] They concluded that these virus specific CTLs only lyse cells carrying the same molecules of the major histocompatibility site (MHC) as the CTLs themselves. Thus, the virus-specific CTLs are "MHC-restricted".[8] This discovery lead to a greater understanding of an important aspect of the immune system.[citation needed]

Spread

edit

LCMV is naturally spread by the common house mouse, Mus musculus.[12] Once infected, these mice can become chronically infected by maintaining virus in their blood or persistently shedding virus in their urine. Chronically infected female mice usually transmit infection to their offspring (vertical transmission), which in turn become chronically infected. Other modes of mouse-to-mouse transmission include nasal secretions, milk from infected dams, bites, and during social grooming within mouse communities. Airborne transmission also occurs.[13]

The virus seems to be relatively resistant to drying and therefore humans can become infected by inhaling infectious aerosolized particles of rodent urine, feces, or saliva, by ingesting food contaminated with virus, by contamination of mucous membranes with infected body fluids, or by directly exposing cuts or other open wounds to virus-infected blood. The only documented cases of transmission from animals have occurred between humans and mice or hamsters.[citation needed]

Cases of lymphocytic choriomeningitis have been reported in North and South America, Europe, Australia, and Japan, particularly during the 1900s.[14][15] However, infection may occur wherever an infected rodent host population exists.[13] LCMV occurs worldwide and its natural host, the rodent, has become established on all continents, except Antarctica.[7]

Seroprevalence is approximately 5% (0.7–4.7%) of the US population. It tends to be more common among lower socio-economic groupings, probably reflecting more frequent and direct contacts with mice. However, obtaining an accurate sense of prevalence by geographic region is difficult due to underreporting.[15]

Congenital infection

edit

Lymphocytic choriomeningitis is a particular concern in obstetrics, as vertical transmission is known to occur. For immunocompetent mothers, there is no significant threat, but the virus has damaging effects upon the fetus. If infection occurs during the first trimester, LCMV results in an increased risk of spontaneous abortion.[14] Later congenital infection may lead to malformations such as intracranial calcifications, hydrocephalus, microcephaly or macrocephaly, intellectual disabilities, and seizures.[16] Other findings include chorioretinal scars, and optic atrophy. Chorioretinitis, which is followed by chorioretinal scarring, is the most common ocular lesion.[7] Mortality among infants is approximately 30%. Among the survivors, two-thirds have lasting neurologic abnormalities.[14]

Other ocular defects including optic atrophy, microphthalmia, vitreitis, leukokoria and cataracts can also be seen. Most of the infants in one case series were of normal birth weight, although 30% were underweight.[7] Aspiration pneumonia can be a fatal complication. Infants who survive may have severe neurological defects including epilepsy, impaired coordination, visual loss or blindness, spastic diplegia or quadriparesis/quadriplegia, delayed development and intellectual disability.[7] Less severe cases with isolated cerebellar hypoplasia and symptoms of ataxia and jitteriness have been reported occasionally.[7] There have also been rare cases with evidence of chorioretinitis but without neurological signs. Systemic signs seem to be rare, but hepatosplenomegaly, thrombocytopenia and hyperbilirubinemia have been documented in a few cases, and skin blisters were reported in one infant.[7]

If a woman has come into contact with a rodent during pregnancy and LCM symptoms are manifested, a blood test is available to determine previous or current infection. A history of infection does not pose a risk for future pregnancies.[17]

Organ donation

edit

Patients infected in solid organ transplants have developed a severe fatal illness, starting within weeks of the transplant.[7] In all reported cases, the initial symptoms included fever, lethargy, anorexia and leukopenia, and quickly progressed to multisystem organ failure, hepatic insufficiency or severe hepatitis, dysfunction of the transplanted organ, coagulopathy, hypoxia, multiple bacteremias and shock.[7] Localized rash and diarrhea were also seen in some patients. Nearly all cases have been fatal.[7]

In May 2005, four solid-organ transplant recipients contracted an illness that was later diagnosed as lymphocytic choriomeningitis. All received organs from a common donor, and within a month of transplantation, three of the four recipients had died as a result of the viral infection.[18] Epidemiologic investigation traced the source to a pet hamster that the organ donor had recently purchased from a Rhode Island pet store.[6] Similar cases occurred in Australia in 2006[19][20] and Massachusetts in 2008. There is not a LCMV infection test that is approved by the Food and Drug Administration for organ donor screening. The Morbidity and Mortality Weekly Report advises health-care providers to "consider LCMV infection in patients with aseptic meningitis and encephalitis and in organ transplant recipients with unexplained fever, hepatitis, or multisystem organ failure."[21]

Diagnosis

edit

Current or previous infection can be detected through a blood test.[17] However, some authors note that such complement-fixation tests are insensitive and should not be used for diagnosis.[14] Dr. Clare A. Dykewicz, et al. state,

Infection with LCMV should be considered in the differential diagnosis of any compatible, severe viral infection or aseptic meningitis, especially when there is a history of occupational exposure to laboratory rodents. Timeliness of diagnosis is important not only in expediting treatment of infected persons, but also in preventing further LCMV transmission to other workers and animals.[22]

Clinical diagnosis of LCM can be made by the history of prodrome symptoms and by considering the period of time before the onset of meningitis symptoms, typically 15–21 days for LCM.[3]

Pathological diagnosis of congenital infection is performed using either an immunofluorescent antibody (IFA) test or an enzyme immunoassay to detect specific antibody in blood or cerebrospinal fluid. A PCR assay has been recently developed which may be used in the future for prenatal diagnosis; however, the virus is not always present in the blood or CSF when the affected child is born."[14] Diagnoses is subject to methodological shortcomings in regard to specificity and sensitivity of assays used.[23] For this reason, LCMV may be more common than is realized.[14]

Another detection assay is the reverse transcription polymerase chain reaction (RT-PCR) tests which may detect nucleic acids in the blood and cerebrospinal fluid.(CSF)[7] Virus isolation is not used for diagnosis in most cases but it can be isolated from the blood or nasopharyngeal fluid early in the course of the disease,[7] or from CSF in patients with meningitis. LCMV can be grown in a variety of cell lines including BHK21, L and Vero cells, and it may be identified with immuno-fluorescence.[7] A diagnosis can also be made by the intracerebral inoculation of blood or CSF into mice.[7]

Prevention

edit

LCMV is susceptible to most detergents and disinfectants including 1% sodium hypochlorite, 70% ethanol, 2% glutaraldehyde and formaldehyde.[7] The effectiveness of infection quickly declines below pH 5.5 and above pH 8.5. In addition, LCMV can also be inactivated by heat, ultraviolet light or gamma irradiation.[7]

Studies have indicated that human infection of the virus occurs primarily during the fall and winter months, presumably due to the movement of mice indoors.[16][24] Several measures can be taken to prevent exposure to LCM from wild rodents in the home. A checklist of precautions is provided by the Centers for Disease Control and Prevention, providing tips for sealing the home to keep rodents out, using traps to eliminate existing rodents, and maintaining a clean, healthy home.[25] New technology reflects a growing trend for more humane means of eliminating rodents. Products include devices that emit ultrasonic sound that allegedly irritates mice and drives them away, and more swift, painless means of death such as mini electrocution or gas chambers. However, the traditional snap trap remains an economic and popular option.[24]

Treatment

edit

Treatment is symptomatic and supportive. Children with hydrocephalus often need a ventriculoperitoneal shunt.[7] Nucleoside analog ribavirin is used in some cases due to the inhibitory effect the agent has in vitro on arenaviruses.[14] However, there is not sufficient evidence for efficacy in humans to support routine use.[26] The only survivor of a transplant-associated LCMV infection was treated with ribavirin and simultaneous tapering of the immunosuppressive medications.[7] Early and intravenous ribavirin treatment is required for maximal efficacy, and it can produce considerable side effects.[27] Ribavirin has not been evaluated yet in controlled clinical trials.[citation needed]

Use of ribavirin during pregnancy is generally not recommended, as some studies indicate the possibility of teratogenic effects. If aseptic meningitis, encephalitis, or meningoencephalitis develops in consequence to LCMV, hospitalization and supportive treatment may be required. In some circumstances, anti-inflammatory drugs may also be considered.[14] In general, mortality is less than one percent.[21]

Prognosis

edit

Lymphocytic choriomeningitis is not a commonly reported infection in humans, though most infections are mild and are often never diagnosed. Serological surveys suggest that approximately 1–5% of the population in the U.S. and Europe has antibodies to LCMV.[7] The prevalence varies with the living conditions and exposure to mice, and it has been higher in the past due to lower standards of living. The island of Vir in Croatia is one of the biggest described endemic places of origin of LCMV in the world, with IFA testing having found LCMV antibodies in 36% of the population.[28][29] Individuals with the highest risk of infection are laboratory personnel who handle rodents or infected cells.[7] Temperature and time of year is also a critical factor that contributes to the number of LCMV infections, particularly during fall and winter[7] when mice tend to move indoors. Approximately 10–20%[7] of the cases in immunocompetent individuals are thought to progress to neurological disease, mainly as aseptic meningitis. The overall case fatality rate is less than 1%[7] and people with complications, including meningitis, almost always recover completely. Rare cases of meningoencephalitis have also been reported.[7] More severe disease is likely to occur in people who are immunosuppressed.[7]

More than 50 infants with congenital LCMV infection have been reported worldwide.[7] The probability that a woman will become infected after being exposed to rodents, the frequency with which LCMV crosses the placenta, and the likelihood of clinical signs among these infants are still poorly understood. In one study, antibodies to LCMV were detected in 0.8% of normal infants,[7] 2.7% of infants with neurological signs[7] and 30% of infants with hydrocephalus.[7] In Argentina, no congenital LCMV infections were reported among 288 healthy mothers and their infants.[7] However, one study[7] found that two of 95 children in a home for people with severe mental disabilities had been infected with this virus. The prognosis for severely affected infants appears to be poor. In one series, 35% of infants diagnosed with congenital infections had died by the age of 21 months.[7]

Transplant-acquired lymphocytic choriomeningitis proves to have a very high morbidity and mortality rate. In the three clusters reported in the U.S. from 2005 to 2010,[7] nine of the ten infected recipients died.[7] One donor had been infected from a recently acquired pet hamster[7] while the sources of the virus in the other cases were unknown.

Epidemiology

edit

LCMV has been isolated from fleas, ticks, cockroaches, Culicoides and Aedes mosquitoes. Ticks, lice and mosquitoes have been shown to transmit this virus mechanically in the laboratory.[7] The presence of LCMV in laboratories may cause serious long-term repercussions to worker safety. In 1989, an outbreak among humans occurred in a US cancer research institute that studied the effects of various therapeutic and diagnostic agents in animal models. Such agents had been developed in the animal care facility, which periodically screened sentinel animals for extraneous infection. Due to an oversight, no sentinel animals were monitored from August 1988 to March 1989. When testing resumed, LCMV antibodies were found in the oldest sentinel hamsters. Several workers reported symptoms consistent with LCMV infection, leading to an investigation. Blood samples were obtained and tested for LCMV antibodies. Of the 82 workers that were tested, seven had definite serologic evidence of past LCMV infection, and two were hospitalized for an acute febrile illness. All seven reported direct contact with the animals at the institute.[22]

An additional hazard associated with LCMV in laboratories misleading experimental results.[22] Interference with research may involve:

[Inhibition of] tumor induction due to polyoma virus, and mammary tumor virus in the mouse, and [interference] with transplantable leukaemia in the guinea pig and the mouse. Infection is associated with depression of cellular immunity in the mouse. Rejection of cutaneous grafts or transplantable tumors may be delayed. In addition, infection will increase the sensitivity of the mouse to ectromelia virus and to bacterial endotoxins.[30]

Reported outbreaks have decreased, perhaps due to improved biohazard management in laboratories. However, it is possible that sporadic cases have been overlooked because of the wide range of clinical presentations. Clare A. Dykewicz, et al. recommend vigilant screening laboratory animals to be used in research facilities either through serum samples or cell line aliquots, as well as ensuring adequate ventilation in housing areas and use of appropriate sanitation products.[22] Other practices to reduce cross-contamination in rodents include washing hands or changing gloves between animal care activities, thoroughly decontaminating cages before reusing them, and avoiding housing healthy rodents in the vicinity of potentially infected rodents.[6]

Other animals

edit

Although the house mouse (Mus musculus) is the primary reservoir host for LCMV, it is also often found in the wood mouse (Apodemus sylvaticus) and the yellow-necked mouse (Apodemus flavicollis).[7] Hamster populations can act as reservoir hosts. Other rodents including guinea pigs, rats and chinchillas can be infected but do not appear to maintain the virus.[7] LCMV has been shown to cause illness in New World primates such as macaques, marmosets and tamarins.[7] Infections have also been reported in rabbits, dogs and pigs.[7] After experimental inoculation, the incubation period in adult mice is 5 to 6 days.[7] Congenitally or neonatally infected mice and hamsters do not become symptomatic for several months or longer.[7]

Mice

edit
 
A house mouse Mus musculus

A study conducted by John Hotchin and Heribert Weigand, of the New York State Department of Health, concluded, "The age of the mouse when first exposed to the virus determines its immune response." If LCMV infection occurs in utero or within the first few hours of life, during the immunologically unresponsive period, the mouse will develop immune tolerance. The virus will continue to proliferate for an indefinite time. However, if a mouse is infected after the neonatal period, when the immune system is responsive, the immune response is active. This immunological conflict can result in one of three ways; immunological paralysis, significant or complete suppression of virus with immunity to reinfection, or death. Mice that are infected after the neonatal period often pass through a "runt" stage, which may last for several weeks. Clinical symptoms include excitability, weight loss, and severe retardation of growth and hair development. In general, as the period of time between birth and inoculation decreases, less disease and mortality occurs.[31]

Post mortem lesions in mice show signs of hepatomegaly, splenomegaly, lymphadenopathy, and swollen or shrunken and pitted kidneys due to glomerulonephritis.[7] Histological findings in persistently infected mice often show chronic glomerulonephritis.[7] In these mice, and some hamsters, vasculitis and lymphocytic infiltrates in many organs and tissues including the liver, spleen, lung, kidneys, pancreas, blood vessels, meninges and brain are present.[7]

Hamsters

edit

Pathogenesis occurs in the same manner in hamsters as in mice.[32] Symptoms in hamsters are highly variable, and typically indicate that the pet has been infected and shedding the virus for several months. Early signs may include inactivity, loss of appetite, and a rough coat. As the disease progresses, the animal may experience weight loss, hunched posture, inflammation around the eyes, and eventually death. Alternatively, some infected hamsters may be asymptomatic.[33]

Rats

edit

Experimental intracerebral infection of suckling rats results in microcephaly, retinitis and the destruction of several brain regions,[7] leading to permanent abnormalities of movement, coordination, vision and behavior.

Primates

edit

LCMV causes callitrichid hepatitis[7] in New World primates. The onset of the infection is nonspecific and may include fever, anorexia, dyspnea, weakness and lethargy. Jaundice is characteristic and petechial hemorrhages may develop.[7] Prostration and death usually follow.[7] Necropsy lesions in primates with callitrichid hepatitis show signs of jaundice, hepatomegaly, splenomegaly, and subcutaneous and intramuscular hemorrhages.[7] Pleural and pericardial effusion, sometimes sanguineous, has also been reported.[7] On histology, multifocal necrosis with acidophilic bodies and mild inflammatory infiltrates are typically found in the liver.[7]

Diagnosis

edit

As in humans, the sensitivity of testing methods for rodents contributes to the accuracy of diagnosis. LCMV is typically identified through serology. However, in an endemically infected colony, more practical methods include MAP (mouse antibody production) and PCR testing. Another means of diagnosis is introducing a known naïve adult mouse to the suspect rodent colony. The introduced mouse will seroconvert, allowing use of immunofluorescence antibody (IFA), MFIA or ELISA to detect antibodies.[30]

Treatment

edit

Immunosuppressive therapy has been effective in halting the disease for laboratory animals.[32]

Morbidity and mortality

edit

LCMV infections are focal[7] Estimates of its prevalence in wild mouse populations range from 0% to 60%, with an average prevalence of 9%.[7] The incidence of LCMV in pet rodents is unknown, yet very few human cases have been associated with exposure to pets.[7] In the transplant-associated cases linked to a pet hamster in 2005, two other hamsters and a guinea pig at the pet shop, and approximately 4%[7] of the hamsters at the distributor, were also infected. Morbidity and mortality rates vary with the species of animal and its age at infection,[7] as well as the strain of the virus and route of exposure. Neonatally and congenitally infected mice remain asymptomatic for many months, but the onset of glomerulonephritis[7] reduces overall life expectancy. The morbidity rate in naturally infected post-neonatal mice is unknown; however, subclinical disease may be the most common form, as few natural outbreaks have been reported.[7] In hamsters, approximately half of all congenitally infected animals[7] clear the virus when they are approximately three months old and remain healthy; the remaining animals develop chronic disease.[7] Hamsters infected as adults usually remain asymptomatic. Callitrichid hepatitis[7] is reported to be highly fatal in naturally infected marmosets and tamarins in zoos. Since 1980, 12 outbreaks with 57 deaths[7] have been reported in the U.S. In experimentally infected rhesusmacaques, three of four animals[7] became fatally ill when inoculation was by the intravenous route. In contrast, inoculation by the intragastric route usually led to asymptomatic infections, with occasional disease and few deaths.[7]

In pets

edit

Pet rodents are not known to be natural reservoirs for lymphocytic choriomeningitis virus. However, pets can become vectors if they are exposed to wild house mice in a breeding facility, pet store, or home. Such infections are rare.[33] To date, (January 2017) documented infections in humans have occurred only after introduction to infected mice, guinea pigs, and hamsters, with the majority of cases transmitted by mice. LCMV infection in other animals, including zoo animals, may be possible.[6][23]

In choosing a pet, the CDC advises looking for general indications of health both in the prospective pet and others in the facility. The rodent of choice should be lively and alert, have a glossy coat, breathe normally and have no discharge from eyes or nose. If one of the animals in the facility looks ill, the others may have been exposed, and none of the rodents at that location should be purchased.[33]

Serologic testing is not recommended for pet rodents, as it has been unreliable in detecting antibodies in animals with active infections. For laboratory purposes, immunohistochemistry staining of tissues and virus isolation are used for more accurate testing, but this is unnecessary for the general house pet. The greatest risk of infection to humans occurs shortly after purchase of a pet, so that exposure to the virus, if present, has likely already occurred to existing pet owners. Continued ownership poses negligible additional risk.[6]

The National Center for Infectious Disease suggests the following precautions to reduce the risk of LCMV infection:

  • Wash hands with soap and water after handling pet rodents; use waterless alcohol-based hand rubs when soap is not available.
  • Keep rodent cages clean and free of soiled bedding.
  • Clean the cage in a well-ventilated area or outside.
  • Wash hands thoroughly with soap and water after cleaning up pet droppings. Closely supervise young children, especially those less than five years old, when cleaning cages, and make sure they wash their hands immediately after handling rodents and rodent caging or bedding.
  • Do not kiss pet rodents or hold them close to your face.[33]

Rodent owners who no longer wish to keep their pet should consult a veterinarian. Pets should not be released into the wild for humane, legal, and ecological reasons. After a rodent has been purchased, it should not be returned to the pet store as it may have been exposed to LCMV through house mice.[5]

Research

edit

LCM is the archetypal arenavirus, and was instrumental in research which uncovered the major pathogenetic mechanisms of all arenaviruses.[34]

The field of viral immunology will continue to be uncovered by the model system of LCMV. Specifically, the study of persistent viral infections as well as vaccine development, represent two essential areas.[8] LCMV is already identified as the best model to examine the difference between acute and persistent infection in its natural host Mus musculus, the common house mouse. Conveniently, the mouse is also the most widely used genetic model for mammalian genetics. A major phenotypic difference results from only two nucleotide differences[8] between acute LCMV, also known as Armstrong LCMV, and one of its variant, Clone 13, which leads to persistent LCMV infection. One of the nucleotide mutations is in the process of glycoprotein formation and affects tropism.[8] The second base pair mutation affects the polymerase which influences replicative capacity.[8] The mechanism by which these mutations cause acute versus chronic LCMV infection is not understood.[citation needed]

An important aspect of the present modern society is the thorough understanding of the burden of cancer.[8] In many ways, this disease mirrors persistent viral infection, in the way that it evades and progresses despite the immune system's effort to eliminate it.[8] The LCMV model will be a great path towards advancements in cancer studies. Furthermore, LCMV has been a widely used model system for understanding T cell memory[8] and vaccine synthesis. It was the original model when first studied focused on CD8 T cells response towards LCMV infection.[8] In addition, a better understanding of CD4+ T cell memory is also a result of studies with LCMV and will continue to contribute to a more efficient mechanism of vaccine formation. Specifically, LCMV has been recently used to quantify the efficiency of a new hydrogen peroxide-based vaccine formation mechanism.[8] The future enhancement of the field of vaccinology will greatly depend on the LCMV model system.[citation needed]

LCMV is a prototype of more severe hemorrhagic fever viruses,[8] especially Lassa virus with the greatest prevalence in sub-Saharan Africa.[8] However, other strains of this virus (Junin and Machupo viruses)[8] are present in parts of South America and other strains continue to significantly affect the southern African population. Since the modern society continue to become a more inter-connected world, the spread of these virus strains will continue to pose a severe threat around the globe. Understanding the biology of the LCMV model virus will help in advancing the understanding of this important class of viruses and more specifically will give insight into the biology of the Lassa virus which proves to be a growing threat around the world. Furthermore, the United States National Institute of Allergy and Infectious Diseases (NIAID)[8] has appointed the family of arenaviridae to be "Category A Priority Pathogens".[8] This translates to the highest level of importance for the high potential for morbidity and mortality from an infectious agent which is relatively easy to produce and transmit.[8]

Footnotes

edit
  1. ^ Beeman op. cit. pp. 305f.
  2. ^ Edward A. Beeman: Charles Armstrong, M.D.: A Biography, 2007 pp. 183ff. (also online here (PDF) Archived 28 April 2017 at the Wayback Machine
  3. ^ a b Lasker, Jill S. "Lymphocytic choriomeningitis".
  4. ^ "choriomeningitis"
  5. ^ a b CDC. "Information for Pet Owners: Reducing the Risk of Becoming Infected with LCMV from Pet Rodents".
  6. ^ a b c d e United States. Div of Viral and Rickettsial Diseases, National Center for Infectious Diseases, CDC (August 2005). "Update: interim guidance for minimizing risk for human lymphocytic choriomeningitis virus infection associated with pet rodents". MMWR Morb. Mortal. Wkly. Rep. 54 (32): 799–801. PMID 16107785.
  7. ^ a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br The centre for Food Security and Public Health. Institute for International Co-operation and in Animal Biologics. Iowa State University. Ames, Iowa. 2010. http://www.cfsph.iastate.edu/Factsheets/pdfs/lymphocytic_choriomeningitis.pdf
  8. ^ a b c d e f g h i j k l m n o p q r s t u v w Zhou X, Ramachandran S, Mann M, Popkin DL (October 2012). "Role of lymphocytic choriomeningitis virus (LCMV) in understanding viral immunology: past, present and future". Viruses. 4 (11): 2650–69. doi:10.3390/v4112650. PMC 3509666. PMID 23202498.
  9. ^ a b c d e f Lee KJ, Novella IS, Teng MN, Oldstone M, de la Torre JC (2000). "NP and L Proteins of Lymphocytic Choriomeningitis Virus (LCMV) Are Sufficient for Efficient Transcription and Replication of LCMV Genomic RNA Analog". Journal of Virology. 74 (8): 3470–7. doi:10.1128/jvi.74.8.3470-3477.2000. PMC 111854. PMID 10729120.
  10. ^ [27]
  11. ^ a b c d e Swiss Institute of Bioinformatics. Viral Zone "Arenaviridae".
  12. ^ Hill, A. Edward (1948). "Benign lymphocytic meningitis". Caribbean Medical Journal. XI (1): 34–7.
  13. ^ a b Childs JE, Glass GE, Korch GW, Ksiazek TG, Leduc JW (July 1992). "Lymphocytic choriomeningitis virus infection and house mouse (Mus musculus) distribution in urban Baltimore". Am. J. Trop. Med. Hyg. 47 (1): 27–34. doi:10.4269/ajtmh.1992.47.27. PMID 1636880.
  14. ^ a b c d e f g h Jamieson DJ, Kourtis AP, Bell M, Rasmussen SA (June 2006). "Lymphocytic choriomeningitis virus: an emerging obstetric pathogen?". Am. J. Obstet. Gynecol. 194 (6): 1532–6. doi:10.1016/j.ajog.2005.11.040. PMID 16731068.
  15. ^ a b CDC. "Lymphocytic choriomeningitis."
  16. ^ a b Barton LL, Hyndman NJ (March 2000). "Lymphocytic choriomeningitis virus: reemerging central nervous system pathogen". Pediatrics. 105 (3): E35. doi:10.1542/peds.105.3.e35. PMID 10699137. S2CID 10452284.
  17. ^ a b CDC. "Lymphocytic Choriomeningitis Virus (LCMV) and Pregnancy: Facts and Prevention."
  18. ^ Emonet S, Retornaz K, Gonzalez JP, de Lamballerie X, Charrel RN (March 2007). "Mouse-to-human transmission of variant lymphocytic choriomeningitis virus". Emerging Infect. Dis. 13 (3): 472–75. doi:10.3201/eid1303.061141. PMC 2725903. PMID 17552104.
  19. ^ Jamieson A (7 May 2013). "Inquest into the Death of Carmelina Sirianni" (PDF). Coroner's Court of Victoria.
  20. ^ Transplant patients died from donor's disease—Australian Broadcasting Corporation—Retrieved 7 May 2013.
  21. ^ a b Centers for Disease Control and Prevention (July 2008). "Brief report: Lymphocytic choriomeningitis virus transmitted through solid organ transplantation—Massachusetts, 2008". MMWR Morb. Mortal. Wkly. Rep. 57 (29): 799–801. PMID 18650788.
  22. ^ a b c d Dykewicz CA, Dato VM, Fisher-Hoch SP, et al. (March 1992). "Lymphocytic choriomeningitis outbreak associated with nude mice in a research institute". JAMA. 267 (10): 1349–53. doi:10.1001/jama.1992.03480100055030. PMID 1740856.
  23. ^ a b Craighead, John E. MD. Pathology and Pathogenesis of Human Viral Disease.
  24. ^ a b Bauers, Sandy. "House vs. Mouse: The Latest Ideas in Humanely Showing Our Disease-Ridden Fall Visitors the Door."
  25. ^ CDC. "Prevent LCMV from wild rodents."p. 1. [1] Archived 10 August 2013 at the Wayback Machine
  26. ^ CDC. "Lymphocytic choriomeningitis."
  27. ^ Emonet SF, Garidou L, McGavern DB, de la Torre JC (March 2009). "Generation of recombinant lymphocytic choriomeningitis viruses with trisegmented genomes stably expressing two additional genes of interest". Proc. Natl. Acad. Sci. U.S.A. 106 (9): 3473–8. Bibcode:2009PNAS..106.3473E. doi:10.1073/pnas.0900088106. PMC 2651270. PMID 19208813.
  28. ^ Kalenić S (2013). Medicinska mikrobiologija [Medical Microbiology] (in Croatian). Zagreb: Medicinska naklada. ISBN 978-953-176-637-1.
  29. ^ Dobec M, Dzelalija B, Punda-Polic V, Zoric I (2006). "High prevalence of antibodies to lymphocytic choriomeningitis virus in a murine typhus endemic region in Croatia". J. Med. Virol. 78 (12): 1643–7. doi:10.1002/jmv.20749. PMID 17063527. S2CID 26136748.
  30. ^ a b Charles River Laboratories International. "Lymphocytic Choriomeningitis Virus."
  31. ^ Hotchin J, Weigand H (April 1961). "Studies of lymphocytic choriomeningitis in mice. I. The relationship between age at inoculation and outcome of infection". J. Immunol. 86 (4): 392–400. doi:10.4049/jimmunol.86.4.392. PMID 13716107. S2CID 255639697.
  32. ^ a b Vilches, Jose MD ed. Pam Mouser, MD. "Lymphocytic Choriomeningitis."
  33. ^ a b c d CDC. "Lymphocytic Choriomeningitis Virus from Pet Rodents."
  34. ^ Hotchin J (1977). "Experimental animals and in vitro systems in the study of lymphocytic choriomeningitis virus". Bull. World Health Organ. 55 (5): 599–603. PMC 2366689. PMID 338190.

References

edit

Further reading

edit
edit
Retrieved from "https://en.wikipedia.org/w/index.php?title=Lymphocytic_choriomeningitis&oldid=1257811925"