exudates and Encephalitis--Viral

exudates has been researched along with Encephalitis--Viral* in 42 studies

Reviews

8 review(s) available for exudates and Encephalitis--Viral

ArticleYear
Nipah Virus: Past Outbreaks and Future Containment.
    Viruses, 2020, 04-20, Volume: 12, Issue:4

    Viral outbreaks of varying frequencies and severities have caused panic and havoc across the globe throughout history. Influenza, small pox, measles, and yellow fever reverberated for centuries, causing huge burden for economies. The twenty-first century witnessed the most pathogenic and contagious virus outbreaks of zoonotic origin including severe acute respiratory syndrome coronavirus (SARS-CoV), Ebola virus, Middle East respiratory syndrome coronavirus (MERS-CoV) and Nipah virus. Nipah is considered one of the world's deadliest viruses with the heaviest mortality rates in some instances. It is known to cause encephalitis, with cases of acute respiratory distress turning fatal. Various factors contribute to the onset and spread of the virus. All through the infected zone, various strategies to tackle and enhance the surveillance and awareness with greater emphasis on personal hygiene has been formulated. This review discusses the recent outbreaks of Nipah virus in Malaysia, Bangladesh and India, the routes of transmission, prevention and control measures employed along with possible reasons behind the outbreaks, and the precautionary measures to be ensured by private-public undertakings to contain and ensure a lower incidence in the future.

    Topics: Animals; Bangladesh; Chiroptera; Disease Outbreaks; Encephalitis, Viral; Henipavirus Infections; Humans; India; Infection Control; Malaysia; Nipah Virus; Viral Structural Proteins

2020
Epidemiology, surveillance and control of Nipah virus infections in Malaysia.
    The Malaysian journal of pathology, 2010, Volume: 32, Issue:2

    The outbreak of Nipah virus, affecting pigs and pig-farm workers, was first noted in September 1998 in the north-western part of peninsular Malaysia. By March 1999, the outbreak had spread to other pig-farming areas of the country, inclusive of the neighbouring country, Singapore. A total of 283 human cases of viral encephalitis with 109 deaths were recorded in Malaysia from 29 September 1998 to December 1999. During the outbreak period, a number of surveillances under three broad groups; Surveillance in Human Health Sector, Surveillance in Animal Health Sector, and Surveillance for the Reservoir Hosts, were carried out to determine the prevalence, risk of virus infections and transmission in human and swine populations as well as the source and reservoir hosts of Nipah virus. Surveillance data showed that the virus spread rapidly among pigs within infected farms and transmission was attributed to direct contact with infective excretions and secretions. The spread of the virus among pig farms within and between states of peninsular Malaysia was due to movement of pigs. The transmission of the virus to humans was through close contact with infected pigs. Human to human transmission was considered a rare event though the Nipah virus could be isolated from saliva, urine, nasal and pharyngeal secretions of patients. Field investigations identified fruitbats of the Pteropid species as the natural reservoir hosts of the viruses. The outbreak was effectively brought under control following the discovery of the virus and institution of correct control measures through a combined effort of multi-ministerial and multidisciplinary teams working in close co-operation and collaboration with other international agencies.

    Topics: Animals; Disease Outbreaks; Encephalitis, Viral; Henipavirus Infections; Humans; Infection Control; Malaysia; Nipah Virus; Population Surveillance; Swine; Swine Diseases

2010
Risk factors, prevention and communication strategy during Nipah virus outbreak in Malaysia.
    The Malaysian journal of pathology, 2010, Volume: 32, Issue:2

    An outbreak of acute febrile encephalitis affecting pig-farm workers and owners was recognized in peninsular Malaysia as early as September 1998. The outbreak was initially thought to be due to Japanese encephalitis (JE) virus and thus very intensive prevention, control and communication strategies directed at JE virus were undertaken by the Ministry of Health and Ministry of Agriculture of Malaysia. There was an immediate change in the prevention, control and communication strategies with focus and strategies on infected pigs as the source of infections for humans and other animals following the discovery of Nipah virus. Information and understanding the risks of Nipah virus infections and modes of transmission strengthened the directions of prevention, control and communication strategies. A number of epidemiological surveillances and field investigations which were broadly divided into 3 groups covering human health sector, animal health sector and reservoir hosts were carried out as forms of risk assessment to determine and assess the factors and degree of risk of infections by the virus. Data showed that there was significant association between Nipah virus infection and performing activities involving close contact with pigs, such as processing of piglets, administering injection or medication to pigs, assisting in the birth of piglets, assisting in pig breeding, and handling of dead pigs in the affected farms. A complex process of anthropogenic driven deforestation, climatic changes brought on by El Niño-related drought, forest fire and severe haze, and ecological factors of mixed agro-pig farming practices and design of pig-sties led to the spillovers of the virus from its wildlife reservoir into pig population.

    Topics: Animals; Communication; Disease Outbreaks; Encephalitis, Viral; Henipavirus Infections; Humans; Infection Control; Malaysia; Nipah Virus; Risk Factors; Swine; Swine Diseases

2010
The emergence of Nipah virus, a highly pathogenic paramyxovirus.
    Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2008, Volume: 43, Issue:4

    Nipah virus first emerged in Malaysia and Singapore between 1998 and 1999, causing severe febrile encephalitis in humans with a mortality rate of close to 40%. In addition, a significant portion of those recovering from acute infection had relapse encephalitis and long-term neurological defects. Since its initial outbreak, there have been numerous outbreaks in Bangladesh and India, in which the mortality rate rose to approximately 70%. These subsequent outbreaks were distinct from the initial outbreak, both in their epidemiology and in their clinical presentations. Recent developments in diagnostics may expedite disease diagnosis and outbreak containment, while progress in understanding the molecular biology of Nipah virus could lead to novel therapeutics and vaccines for this deadly pathogen.

    Topics: Bangladesh; Disease Outbreaks; Encephalitis, Viral; Henipavirus Infections; Humans; India; Malaysia; Nipah Virus; Singapore

2008
Lessons from the Nipah virus outbreak in Malaysia.
    The Malaysian journal of pathology, 2007, Volume: 29, Issue:2

    The Nipah virus outbreak in Malaysia (September 1998 to May 1999) resulted in 265 cases of acute encephalitis with 105 deaths, and near collapse of the billion-dollar pig-farming industry. Because it was initially attributed to Japanese encephalitis, early control measures were ineffective, and the outbreak spread to other parts of Malaysia and nearby Singapore. The isolation of the novel aetiological agent, the Nipah virus (NiV), from the cerebrospinal fluid of an outbreak victim was the turning point which led to outbreak control 2 months later. Together with the Hendra virus, NiV is now recognised as a new genus, Henipavirus (Hendra + Nipah), in the Paramyxoviridae family. Efforts of the local and international scientific community have since elucidated the epidemiology, clinico-pathophysiology and pathogenesis of this new disease. Humans contracted the infection from close contact with infected pigs, and formed the basis for pig-culling that eventually stopped the outbreak. NiV targeted medium-sized and small blood vessels resulting in endothelial multinucleated syncytia and fibrinoid necrosis. Autopsies revealed disseminated cerebral microinfarctions resulting from vasculitis-induced thrombosis and direct neuronal involvement. The discovery of NiV in the urine and saliva of Malaysian Island flying foxes (Pteropus hypomelanus and Petropus vampyrus) implicated these as natural reservoir hosts of NiV. It is probable that initial transmission of NiV from bats to pigs occurred in late 1997/early 1998 through contamination of pig swill by bat excretions, as a result of migration of these forest fruitbats to cultivated orchards and pig-farms, driven by fruiting failure of forest trees during the El Nino-related drought and anthropogenic fires in Indonesia in 1997-1998. This outbreak emphasizes the need for sharing information of any unusual illnesses in animals and humans, an open-minded approach and close collaboration and co-ordination between the medical profession, veterinarians and wildlife specialists in the investigation of such illnesses. Environmental mismanagement (such as deforestation and haze) has far-reaching effects, including encroachment of wildlife into human habitats and the introduction of zoonotic infections into domestic animals and humans.

    Topics: Animals; Chiroptera; Disease Outbreaks; Encephalitis, Viral; Henipavirus Infections; Humans; Malaysia; Nipah Virus; Swine

2007
[Progress in the epidemiologic study of Nipah viral encephalitis].
    Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi, 2004, Volume: 25, Issue:6

    Topics: Animals; Encephalitis, Viral; Humans; Incidence; Malaysia; Nipah Virus

2004
Nipah virus outbreak in Malaysia.
    Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2003, Volume: 26, Issue:3

    Nipah virus, a novel paramyxovirus, closely related to Hendra virus emerged in northern part of Peninsular Malaysia in 1998. The virus caused an outbreak of severe febrile encephalitis in humans with a high mortality rate, whereas, in pigs, encephalitis and respiratory diseases but with a relatively low mortality rate. The outbreak subsequently spread to various regions of the country and Singapore in the south due to the movement of infected pigs. Nipah virus caused systemic infections in humans, pigs and other mammals. Histopathological and radiological findings were characteristic of the disease. Fruitbats of Pteropid species were identified as the natural reservoir hosts. Evidence suggested that climatic and anthropogenic driven ecological changes coupled with the location of piggeries in orchard and the design of pigsties allowed the spill-over of this novel paramyxovirus from its reservoir host into the domestic pigs and ultimately to humans and other animals.

    Topics: Agriculture; Animal Husbandry; Animals; Brain Damage, Chronic; Chiroptera; Disease Outbreaks; Disease Reservoirs; Ecology; Encephalitis, Viral; Hematologic Diseases; Housing, Animal; Humans; Malaysia; Paramyxoviridae Infections; Paramyxovirinae; Population Surveillance; Radiography; Recurrence; Respiratory Tract Infections; Singapore; Swine; Swine Diseases

2003
[Nipah virus outbreak in Malaysia, 1999].
    Uirusu, 2000, Volume: 50, Issue:1

    Topics: Animals; Disease Outbreaks; Encephalitis, Viral; Humans; Malaysia; Paramyxoviridae Infections; Paramyxovirinae; Prognosis; Swine; Time Factors

2000

Other Studies

34 other study(ies) available for exudates and Encephalitis--Viral

ArticleYear
Detailed analysis of the pathologic hallmarks of Nipah virus (Malaysia) disease in the African green monkey infected by the intratracheal route.
    PloS one, 2022, Volume: 17, Issue:2

    Disease associated with Nipah virus infection causes a devastating and often fatal spectrum of syndromes predominated by both respiratory and neurologic conditions. Additionally, neurologic sequelae may manifest months to years later after virus exposure or apparent recovery. In the two decades since this disease emerged, much work has been completed in an attempt to understand the pathogenesis and facilitate development of medical countermeasures. Here we provide detailed organ system-specific pathologic findings following exposure of four African green monkeys to 2.41×105 pfu of the Malaysian strain of Nipah virus. Our results further substantiate the African green monkey as a model of human Nipah virus disease, by demonstrating both the respiratory and neurologic components of disease. Additionally, we demonstrate that a chronic phase of disease exists in this model, that may provide an important opportunity to study the enigmatic late onset and relapse encephalitis as it is described in human disease.

    Topics: Animals; Chlorocebus aethiops; Disease Models, Animal; Encephalitis, Viral; Henipavirus Infections; Lung Diseases; Malaysia; Male; Nipah Virus

2022
Introduction: Nipah virus--discovery and origin.
    Current topics in microbiology and immunology, 2012, Volume: 359

    Until the Nipah outbreak in Malaysia in 1999, knowledge of human infections with the henipaviruses was limited to the small number of cases associated with the emergence of Hendra virus in Australia in 1994. The Nipah outbreak in Malaysia alerted the global public health community to the severe pathogenic potential and widespread distribution of these unique paramyxoviruses. This chapter briefly describes the initial discovery of Nipah virus and the challenges encountered during the initial identification and characterisation of the aetiological agent responsible for the outbreak of febrile encephalitis. The initial attempts to isolate Nipah virus from the bat reservoir host are also described.

    Topics: Animals; Australia; Chiroptera; Chlorocebus aethiops; Disease Outbreaks; Disease Reservoirs; Encephalitis, Viral; Hendra Virus; Henipavirus Infections; Humans; Malaysia; Nipah Virus; Vero Cells

2012
In enterovirus 71 encephalitis with cardio-respiratory compromise, elevated interleukin 1β, interleukin 1 receptor antagonist, and granulocyte colony-stimulating factor levels are markers of poor prognosis.
    The Journal of infectious diseases, 2012, Sep-15, Volume: 206, Issue:6

    Enterovirus 71 (EV71) causes large outbreaks of hand, foot, and mouth disease (HFMD), with severe neurological complications and cardio-respiratory compromise, but the pathogenesis is poorly understood.. We measured levels of 30 chemokines and cytokines in serum and cerebrospinal fluid (CSF) samples from Malaysian children hospitalized with EV71 infection (n = 88), comprising uncomplicated HFMD (n = 47), meningitis (n = 8), acute flaccid paralysis (n = 1), encephalitis (n = 21), and encephalitis with cardiorespiratory compromise (n = 11). Four of the latter patients died.. Both pro-inflammatory and anti-inflammatory mediator levels were elevated, with different patterns of mediator abundance in the CSF and vascular compartments. Serum concentrations of interleukin 1β (IL-1β), interleukin 1 receptor antagonist (IL-1Ra), and granulocyte colony-stimulating factor (G-CSF) were raised significantly in patients who developed cardio-respiratory compromise (P = .013, P = .004, and P < .001, respectively). Serum IL-1Ra and G-CSF levels were also significantly elevated in patients who died, with a serum G-CSF to interleukin 5 ratio of >100 at admission being the most accurate prognostic marker for death (P < .001; accuracy, 85.5%; sensitivity, 100%; specificity, 84.7%).. Given that IL-1β has a negative inotropic action on the heart, and that both its natural antagonist, IL-1Ra, and G-CSF are being assessed as treatments for acute cardiac impairment, the findings suggest we have identified functional markers of EV71-related cardiac dysfunction and potential treatment options.

    Topics: Biomarkers; Child, Preschool; Encephalitis, Viral; Enterovirus A, Human; Female; Granulocyte Colony-Stimulating Factor; Hand, Foot and Mouth Disease; Humans; Infant; Interleukin 1 Receptor Antagonist Protein; Interleukin-1beta; Malaysia; Male; Prognosis; Transcriptome

2012
Epidemiology. Breaking the chain in Bangladesh.
    Science (New York, N.Y.), 2011, Mar-04, Volume: 331, Issue:6021

    Topics: Animals; Antibodies, Viral; Arecaceae; Bangladesh; Chiroptera; Disease Outbreaks; Disease Reservoirs; Encephalitis, Viral; Henipavirus Infections; Humans; Livestock; Malaysia; Nipah Virus; Pneumonia, Viral

2011
Human enterovirus 71 subgenotype B3 lacks coxsackievirus A16-like neurovirulence in mice infection.
    Virology journal, 2005, Aug-26, Volume: 2

    At least three different EV-71 subgenotypes were identified from an outbreak in Malaysia in 1998. The subgenotypes C2 and B4 were associated with the severe and fatal infections, whereas the B3 virus was associated with mild to subclinical infections. The B3 virus genome sequences had >= 85% similarity at the 3' end to CV-A16. This offers opportunities to examine if there are characteristic similarities and differences in virulence between CV-A16, EV-71 B3 and EV-71 B4 and to determine if the presence of the CV-A16-liked genes in EV-71 B3 would also confer the virus with a CV-A16-liked neurovirulence in mice model infection.. Analysis of human enterovirus 71 (EV-71) subgenotype B3 genome sequences revealed that the 3D RNA polymerase and domain Z of the 3'-untranslating region RNA secondary structure had high similarity to CV-A16. Intracerebral inoculation of one-day old mice with the virus resulted in 16% of the mice showing swollen hind limbs and significantly lower weight gain in comparison to EV-71 B4-infected mice. None of the mice presented with hind leg paralysis typical in all the CV-A16 infected mice. CV-A16 genome sequences were amplified from the CV-A16-infected mice brain but no amplification was obtained from all the EV-71-inoculated mice suggesting that no replication had taken place in the suckling mice brain.. The findings presented here suggest that EV-71 B3 viruses had CV-A16-liked non-structural gene features at the 3'-end of the genome. Their presence could have affected virulence by affecting the mice general health but was insufficient to confer the EV-71 B3 virus a CV-A16-liked neurovirulence in mice model infection.

    Topics: Amino Acid Sequence; Animals; Animals, Newborn; Brain; Disease Outbreaks; Encephalitis, Viral; Enterovirus A, Human; Enterovirus Infections; Genotype; Humans; Malaysia; Mice; Models, Molecular; Molecular Sequence Data; Nucleic Acid Conformation; RNA, Viral; Sequence Alignment; Sequence Analysis, DNA; Sequence Homology; Survival Analysis; Virulence

2005
Nipah encephalitis outbreak in Malaysia.
    Annals of the Academy of Medicine, Singapore, 2003, Volume: 32, Issue:1

    Between September 1998 and June 1999, there was a severe outbreak of viral encephalitis among the pig farm workers in Malaysia.. This is a review of the published literature related to the outbreak with the focus on human diseases.. The encephalitis was caused by a newly discovered paramyxovirus related to Hendra virus, later named Nipah virus. There were 265 patients with acute encephalitis. The disease is thought to spread from pig to man through close contact. The risk of human-to-human spread is thought to below. The disease affected mainly adult Chinese males, half of whom had affected family members. The disease presented mainly as acute encephalitis with a short incubation period of less than two weeks, with the main symptoms of fever, headache, and giddiness followed by coma. Distinctive clinical signs include segmental myoclonus, areflexia and hypotonia, hypertension, and tachycardia. Initial cerebrospinal fluid was abnormal in 75% of patients. Serology was helpful in confirming the diagnosis. Magnetic resonance imaging showed distinctive changes of multiple, discrete, and small high signal lesions, best seen with fluid-attenuated inversion recovery (FLAIR) sequences. Mortality was high at 40% and death was probably due to severe brainstem involvement. The main necropsy finding in acute encephalitis was that of disseminated microinfarction associated with vasculitis and direct neuronal involvement. Ribavirin was able to reduce the mortality by 36%. Relapse encephalitis was seen in 7.5% of those who recovered from acute encephalitis, and late-onset encephalitis in 3.4% of those with initial non-encephalitic or asymptomatic diseases. The mean interval between initial illness and the onset of the complication was 8.4 months. The relapse and late-onset encephalitis which manifested as focal encephalitis arose from recurrent infection.. Nipah virus, a recently discovered paramyxovirus, causes a unique encephalitis with high mortality as well as relapse and late-onset encephalitis. The infection is mainly spread from pigs to man.

    Topics: Agriculture; Animals; Chiroptera; Disease Outbreaks; Disease Reservoirs; Encephalitis, Viral; Malaysia; Paramyxoviridae Infections; Paramyxovirinae; Retrospective Studies; Swine

2003
Relapsed and late-onset Nipah encephalitis.
    Annals of neurology, 2002, Volume: 51, Issue:6

    An outbreak of infection with the Nipah virus, a novel paramyxovirus, occurred among pig farmers between September 1998 and June 1999 in Malaysia, involving 265 patients with 105 fatalities. This is a follow-up study 24 months after the outbreak. Twelve survivors (7.5%) of acute encephalitis had recurrent neurological disease (relapsed encephalitis). Of those who initially had acute nonencephalitic or asymptomatic infection, 10 patients (3.4%) had late-onset encephalitis. The mean interval between the first neurological episode and the time of initial infection was 8.4 months. Three patients had a second neurological episode. The onset of the relapsed or late-onset encephalitis was usually acute. Common clinical features were fever, headache, seizures, and focal neurological signs. Four of the 22 relapsed and late-onset encephalitis patients (18%) died. Magnetic resonance imaging typically showed patchy areas of confluent cortical lesions. Serial single-photon emission computed tomography showed the evolution of focal hyperperfusion to hypoperfusion in the corresponding areas. Necropsy of 2 patients showed changes of focal encephalitis with positive immunolocalization for Nipah virus antigens but no evidence of perivenous demyelination. We concluded that a unique relapsing and remitting encephalitis or late-onset encephalitis may result as a complication of persistent Nipah virus infection in the central nervous system.

    Topics: Adolescent; Adult; Brain; Child; Electroencephalography; Encephalitis, Viral; Female; Follow-Up Studies; Humans; Magnetic Resonance Imaging; Malaysia; Male; Middle Aged; Paramyxoviridae Infections; Paramyxovirinae; Recurrence; Time Factors; Tomography, Emission-Computed, Single-Photon

2002
Emerging and re-emerging diseases in Malaysia.
    Asia-Pacific journal of public health, 2002, Volume: 14, Issue:1

    Emerging and re-emerging infectious diseases have become a major global problem. Malaysia appears to be an epicenter for such infections and in recent years, several outbreaks have occurred resulting in loss of lives and economic hardships. In this paper, we discussed the outbreaks of leptospirosis, enterovirus 71 encephalitis, chikungunya polyarthritis and Nipah encephalitis and how a developing country such as Malaysia managed the situation with the help of international agencies and organisations. Many valuable lessons were learned and by sharing our experience, it is hoped that we will be in a better position to handle future outbreaks and prevent their spread to countries in the region.

    Topics: Alphavirus Infections; Arthritis, Infectious; Chikungunya virus; Communicable Diseases, Emerging; Disease Outbreaks; Encephalitis, Viral; Humans; Leptospirosis; Malaysia

2002
Anthropogenic deforestation, El Niño and the emergence of Nipah virus in Malaysia.
    The Malaysian journal of pathology, 2002, Volume: 24, Issue:1

    In late 1998, a novel paramyxovirus named Nipah virus, emerged in Malaysia, causing fatal disease in domestic pigs and humans with substantial economic loss to the local pig industry. Pteropid fruitbats have since been identified as a natural reservoir host. Over the last two decades, the forest habitat of these bats in Southeast Asia has been substantially reduced by deforestation for pulpwood and industrial plantation. In 1997/1998, slash-and-burn deforestation resulted in the formation of a severe haze that blanketed much of Southeast Asia in the months directly preceding the Nipah virus disease outbreak. This was exacerbated by a drought driven by the severe 1997-1998 El Niño Southern Oscillation (ENSO) event. We present data suggesting that this series of events led to a reduction in the availability of flowering and fruiting forest trees for foraging by fruitbats and culminated in unprecedented encroachment of fruitbats into cultivated fruit orchards in 1997/1998. These anthropogenic events, coupled with the location of piggeries in orchards and the design of pigsties allowed transmission of a novel paramyxovirus from its reservoir host to the domestic pig and ultimately to the human population.

    Topics: Animals; Climate; Conservation of Natural Resources; Disease Outbreaks; Disease Reservoirs; Encephalitis, Viral; Humans; Malaysia; Paramyxoviridae Infections; Paramyxovirinae; Swine; Swine Diseases; Weather; Zoonoses

2002
Nipah encephalitis outbreak in Malaysia, clinical features in patients from Seremban.
    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 2002, Volume: 29, Issue:1

    An outbreak of viral encephalitis occurred among pig industry workers in Malaysia in September 1998 to April 1999. The encephalitis was attributed to a new paramyxovirus, Nipah virus. This is a description of the clinical features of 103 patients treated in the Seremban Hospital with characterization of the prognostic factors.. Clinical case records and laboratory investigations were reviewed. The case definition was: patients from the outbreak area, direct contact or in close proximity with pigs, clinical or CSF features of encephalitis.. The mean age was 38 years, 89% were male, 58% were ethnic Chinese, 78% were pig farm owners or hired workers. The mean incubation period was 10 days. The patients typically presented with nonspecific systemic symptoms of fever, headache, myalgia and sore throat. Seizures and focal neurological signs were seen in 16% and 5% respectively. In the more severe cases, this was followed by drowsiness and deteriorating consciousness requiring ventilation in 61%. Autonomic disturbances and myoclonic jerks were common features. The mortality was high at 41%. Systolic hypertension, tachycardia and high fever were associated with poor outcome. On the other hand, 40% recovered fully. As for the other 19%, the residual neurological signs were mostly mild.. Nipah virus caused an encephalitis illness with short incubation period and high mortality. The prognosis for the survivors was good.

    Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Disease Outbreaks; Encephalitis, Viral; Female; Humans; Malaysia; Male; Middle Aged; Paramyxoviridae Infections; Paramyxovirinae; Prognosis; Risk

2002
The presence of Nipah virus in respiratory secretions and urine of patients during an outbreak of Nipah virus encephalitis in Malaysia.
    The Journal of infection, 2001, Volume: 42, Issue:1

    To study the excretion of Nipah virus in the upper respiratory secretions and urine of infected patients in relation to other clinical features.. Isolation of Nipah virus from the respiratory secretions and urine was made in Vero cells and identified by indirect immunofluorescence assay using anti-Hendra specific hyperimmune mouse ascitic fluid and FITC-conjugated goat anti-mouse IgG.. During the peak outbreak of Nipah virus encephalitis in Malaysia, Nipah virus was isolated from the upper respiratory secretions and urine in eight of 20 patients who were virologically and/or serologically confirmed to be infected with the virus. From these eight patients, Nipah virus was isolated from six throat swab specimens, three urine specimens and only one nasal swab specimen. The positive virus isolation rate was related to the collection of these specimens during the early phase of the illness (P = 0.068). The presence of serum anti-Nipah specific IgM appeared to reduce the chance of isolating the virus (P = 0.049). There was no significant difference in the isolation rate with respect to the age, gender, ethnic group and clinical features associated with grave prognosis and mortality outcome of the patients.. This study shows that it is possible to be infected from secretions of infected patients, but epidemiological survey on close contacts so far did not suggest that human-to-human transmission is common.

    Topics: Adolescent; Adult; Animals; Ascites; Disease Outbreaks; Encephalitis, Viral; Female; Fluorescent Antibody Technique, Indirect; Humans; Immunoglobulin G; Malaysia; Male; Mice; Middle Aged; Nasal Mucosa; Paramyxoviridae Infections; Paramyxovirinae; Pharynx; Prognosis; Respiratory System; Virus Shedding

2001
Treatment of acute Nipah encephalitis with ribavirin.
    Annals of neurology, 2001, Volume: 49, Issue:6

    Nipah virus, a newly identified paramyxovirus caused a severe outbreak of encephalitis in Malaysia with high fatalities. We report an open-label trial of ribavirin in 140 patients, with 54 patients who were managed prior to the availability of ribavirin or refused treatment as control. There were 45 deaths (32%) in the ribavirin arm; 29 deaths (54%) occurred in the control arm. This represents a 36% reduction in mortality (p = 0.011). There was no associated serious side effect. This study suggests that ribavirin is able to reduce the mortality of acute Nipah encephalitis.

    Topics: Adult; Asian People; China; Encephalitis, Viral; Female; Humans; Malaysia; Male; Paramyxovirinae; Retrospective Studies; Ribavirin; Treatment Outcome; Treatment Refusal

2001
Late presentation of Nipah virus encephalitis and kinetics of the humoral immune response.
    Journal of neurology, neurosurgery, and psychiatry, 2001, Volume: 71, Issue:4

    Nipah virus is a newly discovered paramyxovirus transmitted directly from pigs to humans. During a large encephalitis outbreak in Malaysia and Singapore in 1998-9, most patients presented acutely. A 12 year old child is described who developed encephalitis 4 months after exposure to the virus. She was diagnosed by a new indirect IgG enzyme linked immunosorbent assay (ELISA), which is also described. The late presentation and IgG subclass responses had similarities to subacute sclerosing panencephalitis. Nipah virus should be considered in patients with encephalitis even months after their possible exposure.

    Topics: Animals; Antibodies, Viral; Child; Encephalitis, Viral; Enzyme-Linked Immunosorbent Assay; Female; Humans; Immunoglobulin G; Malaysia; Paramyxoviridae Infections; Paramyxovirinae; Swine; Zoonoses

2001
Nipah viral encephalitis or Japanese encephalitis? MR findings in a new zoonotic disease.
    AJNR. American journal of neuroradiology, 2000, Volume: 21, Issue:3

    An epidemic of suspected Japanese encephalitis occurred in Malaysia in 1998-1999 among pig farmers. In neighboring Singapore, an outbreak occurred among pig slaughterhouse workers. It was subsequently established that the causative agent in the outbreak was not the Japanese encephalitis virus but a previously unknown Hendra-like paramyxovirus named Nipah virus.. The brain MR images of eight patients with Nipah virus infection were reviewed. All patients tested negative for acute Japanese encephalitis virus. Seven patients had contrast-enhanced studies and six had diffusion-weighted examinations.. All patients had multiple small bilateral foci of T2 prolongation within the subcortical and deep white matter. The periventricular region and corpus callosum were also involved. In addition to white matter disease, five patients had cortical lesions, three had brain stem involvement, and a single thalamic lesion was detected in one patient. All lesions were less than 1 cm in maximum diameter. In five patients, diffusion-weighted images showed increased signal. Four patients had leptomeningeal enhancement and four had enhancement of parenchymal lesions.. The brain MR findings in patients infected with the newly discovered Nipah paramyxovirus are different from those of patients with Japanese encephalitis. In a zoonotic epidemic, this striking difference in the appearance and distribution of lesions is useful in differentiating these diseases. Diffusion-weighted imaging was advantageous in increasing lesion conspicuity.

    Topics: Abattoirs; Adult; Aged; Agricultural Workers' Diseases; Animals; Brain; Diagnosis, Differential; Disease Outbreaks; Encephalitis, Japanese; Encephalitis, Viral; Female; Humans; Magnetic Resonance Imaging; Malaysia; Male; Middle Aged; Paramyxoviridae Infections; Paramyxovirinae; Singapore; Swine; Swine Diseases; Zoonoses

2000
Clinical features of Nipah virus encephalitis among pig farmers in Malaysia.
    The New England journal of medicine, 2000, Apr-27, Volume: 342, Issue:17

    Between September 1998 and June 1999, there was an outbreak of severe viral encephalitis due to Nipah virus, a newly discovered paramyxovirus, in Malaysia.. We studied the clinical features of the patients with Nipah virus encephalitis who were admitted to a medical center in Kuala Lumpur. The case definition was based on epidemiologic, clinical, cerebrospinal fluid, and neuroimaging findings.. Ninety-four patients with Nipah virus infection were seen from February to June 1999 (mean age, 37 years; ratio of male patients to female patients, 4.5 to 1). Ninety-three percent had had direct contact with pigs, usually in the two weeks before the onset of illness, suggesting that there was direct viral transmission from pigs to humans and a short incubation period. The main presenting features were fever, headache, dizziness, and vomiting. Fifty-two patients (55 percent) had a reduced level of consciousness and prominent brain-stem dysfunction. Distinctive clinical signs included segmental myoclonus, areflexia and hypotonia, hypertension, and tachycardia and thus suggest the involvement of the brain stem and the upper cervical spinal cord. The initial cerebrospinal fluid findings were abnormal in 75 percent of patients. Antibodies against Hendra virus were detected in serum or cerebrospinal fluid in 76 percent of 83 patients tested. Thirty patients (32 percent) died after rapid deterioration in their condition. An abnormal doll's-eye reflex and tachycardia were factors associated with a poor prognosis. Death was probably due to severe brain-stem involvement. Neurologic relapse occurred after initially mild disease in three patients. Fifty patients (53 percent) recovered fully, and 14 (15 percent) had persistent neurologic deficits.. Nipah virus causes a severe, rapidly progressive encephalitis with a high mortality rate and features that suggest involvement of the brain stem. The infection is associated with recent contact with pigs.

    Topics: Adult; Animal Husbandry; Animals; Antibodies, Viral; Cerebrospinal Fluid; Disease Outbreaks; Electroencephalography; Encephalitis, Viral; Female; Humans; Logistic Models; Magnetic Resonance Imaging; Malaysia; Male; Nervous System Diseases; Paramyxoviridae Infections; Paramyxovirinae; Recurrence; Swine

2000
Case-control study of risk factors for human infection with a new zoonotic paramyxovirus, Nipah virus, during a 1998-1999 outbreak of severe encephalitis in Malaysia.
    The Journal of infectious diseases, 2000, Volume: 181, Issue:5

    An outbreak of encephalitis affecting 265 patients (105 fatally) occurred during 1998-1999 in Malaysia and was linked to a new paramyxovirus, Nipah, that infected pigs, humans, dogs, and cats. Most patients were pig farmers. Clinically undetected Nipah infection was noted in 10 (6%) of 166 community-farm controls (persons from farms without reported encephalitis patients) and 20 (11%) of 178 case-farm controls (persons from farms with encephalitis patients). Case patients (persons with Nipah infection) were more likely than community-farm controls to report increased numbers of sick/dying pigs on the farm (59% vs. 24%, P=.001) and were more likely than case-farm controls to perform activities requiring direct contact with pigs (86% vs. 50%, P=.005). Only 8% of case patients reported no contact with pigs. The outbreak stopped after pigs in the affected areas were slaughtered and buried. Direct, close contact with pigs was the primary source of human Nipah infection, but other sources, such as infected dogs and cats, cannot be excluded.

    Topics: Agricultural Workers' Diseases; Animals; Case-Control Studies; Cat Diseases; Cats; Disease Outbreaks; Dog Diseases; Dogs; Encephalitis, Viral; Female; Humans; Malaysia; Male; Occupations; Paramyxoviridae Infections; Paramyxovirinae; Risk Factors; Swine; Swine Diseases; Zoonoses

2000
Risk factors for Nipah virus infection among abattoir workers in Singapore.
    The Journal of infectious diseases, 2000, Volume: 181, Issue:5

    During 10-19 March 1999, 11 workers in 1 of 2 Singaporean abattoirs developed Nipah-virus associated encephalitis or pneumonia, resulting in 1 fatality. A case-control study was conducted to determine occupational risk factors for infection. Case patients were abattoir A workers who had anti-Nipah IgM antibodies; control subjects were randomly selected abattoir A workers who tested negative for anti-Nipah IgM. All 13 case patients versus 26 (63%) of 41 control subjects reported contact with live pigs (P=.01). Swine importation from Malaysian states concurrently experiencing a Nipah virus outbreak was banned on 3 March 1999; on 19 March 1999, importation of Malaysian pigs was banned, and abattoirs were closed. No unusual illnesses among pigs processed during February-March were reported. Contact with live pigs appeared to be the most important risk factor for human Nipah virus infection. Direct contact with live, potentially infected pigs should be minimized to prevent transmission of this potentially fatal zoonosis to humans.

    Topics: Abattoirs; Adult; Animals; Antibodies, Viral; Case-Control Studies; Disease Outbreaks; Encephalitis, Viral; Female; Humans; Immunoglobulin M; Malaysia; Male; Occupational Diseases; Paramyxoviridae Infections; Pneumonia, Viral; Risk Factors; Singapore; Swine; Swine Diseases; Zoonoses

2000
Nipah virus: a recently emergent deadly paramyxovirus.
    Science (New York, N.Y.), 2000, May-26, Volume: 288, Issue:5470

    A paramyxovirus virus termed Nipah virus has been identified as the etiologic agent of an outbreak of severe encephalitis in people with close contact exposure to pigs in Malaysia and Singapore. The outbreak was first noted in late September 1998 and by mid-June 1999, more than 265 encephalitis cases, including 105 deaths, had been reported in Malaysia, and 11 cases of encephalitis or respiratory illness with one death had been reported in Singapore. Electron microscopic, serologic, and genetic studies indicate that this virus belongs to the family Paramyxoviridae and is most closely related to the recently discovered Hendra virus. We suggest that these two viruses are representative of a new genus within the family Paramyxoviridae. Like Hendra virus, Nipah virus is unusual among the paramyxoviruses in its ability to infect and cause potentially fatal disease in a number of host species, including humans.

    Topics: Animals; Antibodies, Viral; Disease Outbreaks; Encephalitis, Viral; Endothelium, Vascular; Genes, Viral; Giant Cells; Humans; Malaysia; Microscopy, Electron; Molecular Sequence Data; Nucleocapsid; Paramyxoviridae Infections; Paramyxovirinae; Phylogeny; Respiratory System; Respiratory Tract Infections; Sequence Analysis, DNA; Singapore; Swine; Swine Diseases; Vasculitis; Viral Proteins

2000
Emerging and re-emerging epidemic encephalitis: a tale of two viruses.
    Neuropathology and applied neurobiology, 2000, Volume: 26, Issue:4

    Two major epidemics of viral encephalitis occurred in Asia in 1997 and 1998. The first was a re-emergence of neurovirulent strains of enterovirus 71, which caused severe encephalomyelitis in children in Malaysia, Taiwan and Japan, on a background of hand, foot and mouth disease. Necropsy studies of patients who died of enterovirus 71 infection showed severe perivascular cuffing, parenchymal inflammation and neuronophagia in the spinal cord, brainstem and diencephalon, and in focal areas in the cerebellum and cerebrum. Although no viral inclusions were detected, immunohistochemistry showed viral antigen in the neuronal cytoplasm. Inflammation was often more extensive than neuronal infection, suggesting that other factors, in addition to direct viral cytolysis, may be involved in tissue damage. The second epidemic of viral encephalitis was the result of a novel paramyxovirus called Nipah, which mainly involved pig handlers in Malaysia and Singapore. Pathological evidence suggested that the endothelium of small blood vessels in the central nervous system was particularly susceptible to infection. This led to disseminated endothelial damage and syncytium formation, vasculitis, thrombosis, ischaemia and microinfarction. However, there was also evidence of neuronal infection by the virus and this may also have contributed to the neurological dysfunction in Nipah encephalitis. Some patients who seemed to recover from the acute symptoms have been re-admitted with clinical findings suggestive of relapsing encephalitis. As these two epidemics indicate, the emergence and re-emergence of viral encephalitides continue to pose considerable challenges to the neuropathologist, in establishing the diagnosis and unravelling the pathogenesis of the neurological disease.

    Topics: Animals; Central Nervous System; Cytopathogenic Effect, Viral; Disease Outbreaks; Encephalitis, Viral; Enterovirus; Enterovirus Infections; Humans; Japan; Kidney; Malaysia; Microcirculation; Paramyxoviridae Infections; Paramyxovirinae; Singapore; Swine; Taiwan; Virulence

2000
Emerging diseases. Malaysian researchers trace Nipah virus outbreak to bats.
    Science (New York, N.Y.), 2000, Jul-28, Volume: 289, Issue:5479

    Scientists are a step closer to unraveling a medical mystery that killed 105 people in Malaysia last year and destroyed the country's pig industry. The Nipah virus, which caused the disease, most likely originated in a native fruit bat species, Malaysian researchers reported here at a meeting last week. They say the findings will help Malaysian health authorities prevent future outbreaks of the Nipah virus. Others see the case as an argument for expanding research into infections that can leap the boundary between animals and humans.

    Topics: Animals; Antibodies, Viral; Chiroptera; Disease Outbreaks; Disease Reservoirs; Encephalitis, Viral; Humans; Malaysia; Paramyxoviridae Infections; Paramyxovirinae; Swine; Swine Diseases; Zoonoses

2000
Encephalitis in the 21 st century.
    Seminars in neurology, 2000, Volume: 20, Issue:3

    As the 21st century begins, several outbreaks of encephalitis have been reported. An examination of these outbreaks brings into focus important epidemiological developments. Specifically, urbanization and encroachment on natural environments, the ease of world travel, and global trade can lead to spread of vectors and viruses from the developing world to the developed world. This review focuses on two recent epidemics of encephalitis: West Nile virus encephalitis in the eastern United States and Nipah virus encephalitis in Malaysia and Singapore. These examples demonstrate spread of a known viral agent from an endemic area to an area in which it had not previously been found and identification of a new viral agent. Infectious diseases in the developed world once considered "exotic" are now potential threats to all patients.

    Topics: Encephalitis, Viral; Forecasting; Humans; Malaysia; New York City; Romania; Singapore; West Nile virus

2000
Risk factors for Nipah virus transmission, Port Dickson, Negeri Sembilan, Malaysia: results from a hospital-based case-control study.
    The Southeast Asian journal of tropical medicine and public health, 2000, Volume: 31, Issue:2

    A hospital-based case-control study of viral encephalitis was carried out at Port Dickson Hospital, in the state of Negeri Sembilan, Malaysia. Between March and May 1999, 69 clinically diagnosed viral encephalitis cases and 31 controls were interviewed. Job histories on pig farming activities were assessed by a group of epidemiologists and veterinary surgeons. Results show that among clinical cases of viral encephalitis, 52 (75.4%) cases were diagnosed to have Nipah virus infection based on positive serology for antibodies to the cross-reacting Hendra virus antigen. The Nipah virus encephalitis was significantly associated with a history of working in pig farms (p < 0.001, OR = 196.0, 95% CI = 20.4-4741.6), history of contact with animals (p < 0.001, OR = 38.3, 95% CI = 8.2-209.0) and with history of direct contact with pigs (p = 0.002, OR = 34.4, 95% CI = 2.6-1,024.4). The Nipah virus infection was also significantly associated with history of feeding/cleaning pigs (p < 0.001, OR = 102, 95% CI = 11.9-2,271.5). These results provide evidence that involvement in pig farming activities is significantly associated with the risk of getting Nipah virus infection. They are potential risk factors for Nipah virus transmission in the major pig-producing area of Bukit Pelandok, Port Dickson Negeri Sembilan.

    Topics: Adolescent; Adult; Aged; Agricultural Workers' Diseases; Animal Husbandry; Animals; Case-Control Studies; Encephalitis, Viral; Female; Humans; Malaysia; Male; Middle Aged; Odds Ratio; Paramyxoviridae Infections; Paramyxovirinae; Risk Factors; Swine

2000
Assessment of Nipah virus transmission among pork sellers in Seremban, Malaysia.
    The Southeast Asian journal of tropical medicine and public health, 2000, Volume: 31, Issue:2

    Between September 1998 and May 1999, 265 cases of encephalitis were reported from among those involved in pig rearing. A few cases were also reported among abattoir workers. This raised questions of the risk of transmission among those who handled raw pork. A serosurvey was conducted among pork sellers in Seremban town, which is about 20 km from one of the pig rearing areas which had reported cases of encephalitis. It was found that out of the 28 pork sellers tested, only one tested positive for Nipah virus antibodies and that this pork seller also worked in an abattoir in the same district, removing the urinary bladders from slaughtered pigs. Based on these findings, it was concluded that the risk of transmission of the virus from handling raw pork appeared to be low.

    Topics: Animals; Cross-Sectional Studies; Disease Outbreaks; Encephalitis, Viral; Female; Humans; Malaysia; Male; Meat; Middle Aged; Occupational Diseases; Paramyxoviridae Infections; Paramyxovirinae; Risk Factors; Swine

2000
Outbreak of Hendra-like virus--Malaysia and Singapore, 1998-1999.
    MMWR. Morbidity and mortality weekly report, 1999, Apr-09, Volume: 48, Issue:13

    During September 29, 1998-April 4, 1999, 229 cases of febrile encephalitis (111 [48%] fatal) were reported to the Malaysian Ministry of Health (MOH). During March 13-19, 1999, nine cases of similar encephalitic illnesses (one fatal) and two cases of respiratory illness occurred among abattoir workers in Singapore. Tissue culture isolation identified a previously unknown infectious agent from ill patients. This report summarizes the preliminary epidemiologic and laboratory investigations of these cases, which indicate that a previously unrecognized paramyxovirus related to, but distinct from, the Australian Hendra virus is associated with this outbreak.

    Topics: Abattoirs; Animal Husbandry; Animals; Cluster Analysis; Disease Outbreaks; Encephalitis, Viral; Humans; Malaysia; Male; Middle Aged; Occupational Diseases; Respirovirus; Respirovirus Infections; Singapore; Swine; Swine Diseases

1999
New virus is identified in Malaysia epidemic.
    BMJ (Clinical research ed.), 1999, May-08, Volume: 318, Issue:7193

    Topics: Animals; Disease Outbreaks; Encephalitis Viruses; Encephalitis, Viral; Humans; Malaysia; Swine; Swine Diseases

1999
From the Centers for Disease Control and Prevention. Outbreak of Hendra-like virus--Malaysia and Singapore, 1998-1999.
    JAMA, 1999, May-19, Volume: 281, Issue:19

    Topics: Abattoirs; Animal Husbandry; Animals; Cluster Analysis; Disease Outbreaks; Encephalitis, Viral; Humans; Malaysia; Male; Middle Aged; Occupational Diseases; Respirovirus; Respirovirus Infections; Singapore; Swine; Swine Diseases

1999
Update: outbreak of Nipah virus--Malaysia and Singapore, 1999.
    MMWR. Morbidity and mortality weekly report, 1999, Apr-30, Volume: 48, Issue:16

    During March 1999, health officials in Malaysia and Singapore, in collaboration with Australian researchers and CDC, investigated reports of febrile encephalitic and respiratory illnesses among workers who had exposure to pigs. A previously unrecognized paramyxovirus (formerly known as Hendra-like virus), now called Nipah virus, was implicated by laboratory testing in many of these cases. Febrile encephalitis continues to be reported in Malaysia but has decreased coincident with mass culling of pigs in outbreak areas. No new cases of febrile illness associated with Nipah virus infection have been identified in Singapore since March 19, 1999, when abattoirs were closed. This report summarizes interim findings from ongoing epidemiologic and laboratory investigations in Malaysia and Singapore.

    Topics: Abattoirs; Animal Husbandry; Animals; Disease Outbreaks; Encephalitis, Viral; Fever; Humans; Malaysia; Occupational Exposure; Respirovirus; Respirovirus Infections; Singapore; Swine; Swine Diseases

1999
Update on the new virus in Malaysia.
    CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne, 1999, Jun-15, Volume: 160, Issue:12

    Topics: Abattoirs; Agricultural Workers' Diseases; Animal Husbandry; Animals; Disease Outbreaks; Encephalitis, Viral; Humans; Malaysia; Morbillivirus; Occupational Diseases; Swine

1999
Trailing a virus.
    Scientific American, 1999, Volume: 281, Issue:2

    Topics: Abattoirs; Adult; Animals; Brain; Chiroptera; Disease Outbreaks; Encephalitis, Japanese; Encephalitis, Viral; Female; Fever; Humans; Malaysia; Male; Occupational Exposure; Paramyxoviridae; Paramyxoviridae Infections; Swine; Swine Diseases

1999
The neurological manifestations of Nipah virus encephalitis, a novel paramyxovirus.
    Annals of neurology, 1999, Volume: 46, Issue:3

    A novel Hendra-like paramyxovirus named Nipah virus (NiV) was the cause of an outbreak among workers from one abattoir who had contact with pigs. Two patients had only respiratory symptoms, while 9 patients had encephalitis, 7 of whom are described in this report. Neurological involvement was diverse and multifocal, including aseptic meningitis, diffuse encephalitis, and focal brainstem involvement. Cerebellar signs were relatively common. Magnetic resonance imaging scans of the brain showed scattered lesions. IgM antibodies against Hendra virus (HeV) were present in the serum of all patients. Two patients recovered completely. Five had residual deficits 8 weeks later.

    Topics: Adult; Aged; Brain; Encephalitis, Viral; Humans; Magnetic Resonance Imaging; Malaysia; Male; Middle Aged; Nervous System Diseases; Respirovirus Infections

1999
The Nipah virus outbreak--a reminder.
    Singapore medical journal, 1999, Volume: 40, Issue:5

    Topics: Animals; Birds; Disease Outbreaks; Encephalitis, Viral; Humans; Influenza A virus; Influenza in Birds; Malaysia; Population Surveillance; Public Health; Respirovirus; Respirovirus Infections; Singapore; Zoonoses

1999
Nipah-virus encephalitis--investigation of a new infection.
    Lancet (London, England), 1999, Oct-09, Volume: 354, Issue:9186

    Topics: Adult; Animals; Child; Diagnosis, Differential; Disease Outbreaks; Encephalitis, Viral; Humans; Malaysia; Paramyxoviridae Infections; Paramyxovirinae; Swine

1999
Fatal encephalitis due to Nipah virus among pig-farmers in Malaysia.
    Lancet (London, England), 1999, Oct-09, Volume: 354, Issue:9186

    Between February and April, 1999, an outbreak of viral encephalitis occurred among pig-farmers in Malaysia. We report findings for the first three patients who died.. Samples of tissue were taken at necropsy. Blood and cerebrospinal-fluid (CSF) samples taken before death were cultured for viruses, and tested for antibodies to viruses.. The three pig-farmers presented with fever, headache, and altered level of consciousness. Myoclonus was present in two patients. There were signs of brainstem dysfunction with hypertension and tachycardia. Rapid deterioration led to irreversible hypotension and death. A virus causing syncytial formation of vero cells was cultured from the CSF of two patients after 5 days; the virus stained positively with antibodies against Hendra virus by indirect immunofluorescence. IgM capture ELISA showed that all three patients had IgM antibodies in CSF against Hendra viral antigens. Necropsy showed widespread microinfarction in the central nervous system and other organs resulting from vasculitis-induced thrombosis. There was no clinical evidence of pulmonary involvement. Inclusion bodies likely to be of viral origin were noted in neurons near vasculitic blood vessels.. The causative agent was a previously undescribed paramyxovirus related to the Hendra virus. Close contact with infected pigs may be the source of the viral transmission. Clinically and epidemiologically the infection is distinct from infection by the Hendra virus. We propose that this Hendra-like virus was the cause of the outbreak of encephalitis in Malaysia.

    Topics: Adult; Agricultural Workers' Diseases; Animals; Antibodies, Viral; Disease Outbreaks; Encephalitis, Viral; Fatal Outcome; Humans; Malaysia; Male; Middle Aged; Paramyxoviridae Infections; Paramyxovirinae; Swine

1999
Japanese encephalitis virus is an important cause of encephalitis among children in Penang.
    The Southeast Asian journal of tropical medicine and public health, 1995, Volume: 26, Issue:2

    This study was carried out to determine if Japanese encephalitis virus is an important causative agent of viral encephalitis among pediatric admissions in Penang, Malaysia. 195 children with CNS symptoms and 482 children with non-specific febrile illness admitted into the Pediatric Ward of Penang Hospital during a 16 month period were entered into the study. The presence in serum of cerebrospinal fluid (csf) of Japanese encephalitis virus (JEV) specific IgM was determined by an IgM capture ELISA and cytomegalovirus (CMV) specific IgM was determined using a commercially available kit (Behringwerke AG). It was determined that 5 of 13 children with a discharge diagnosis of viral encephalitis had JEV specific IgM in csf, indicating that 38.5% of the viral encephalitis cases was due to JEV. One of the non-JEV cases was found to have mumps virus specific IgM in csf, while no etiology was determined for the other cases. It was also determined that 4 of the 195 (2.1%) cases with CNS symptoms had IgM to CMV, suggesting CMV may be an agent of encephalopathy in children in Penang. Other viruses found to be associated with CNS symptoms in children admitted into our study were measles and herpes simplex virus. A viral etiology was confirmed for 13 or the 195 cases (6.7%). We also screened 482 non-specific febrile cases for IgM to JEV and to dengue viruses and found that 2 (0.4%) had IgM specific for JEV and 9 (1.9%) had IgM specific for dengue virus.

    Topics: Antibodies, Viral; Child; Child, Preschool; Cytomegalovirus Infections; Encephalitis Virus, Japanese; Encephalitis, Japanese; Encephalitis, Viral; Female; Humans; Immunoglobulin M; Malaysia; Male; Prevalence; Seroepidemiologic Studies

1995