The case fatality rate of Nipah virus infection is estimated at 40–75% but can vary by outbreak depending on surveillance and clinical management in affected areas.[3]
The Nipah virus (NiV) is a type ofRNA virus in the genusHenipavirus, which normally circulates among fruit bats of the genusPteropus.[7] Spread typically requires direct contact with an infected source; it can both spread between people andfrom other animals to people. Diagnosis is based on symptoms and confirmed by laboratory testing.[2][1]
Management is restricted tosupportive care; as of 2021[update] there is neithervaccine nor specific treatment.[2] Preventive measures include avoiding exposure to bats and infected animals such as pigs, and not drinking rawdate palm sap.[1] As of May 2018 about 700 human cases of Nipah virus were estimated to have occurred, and 50 to 75 percent of those infected died.[4][6][5]
The disease was first identified in 1998 by a team of researchers at theFaculty of Medicine, University of Malaya during an outbreak inMalaysia.[8] The majority of the patients in Malaysia diagnosed with the disease were referred to and treated at theUniversity of Malaya Medical Centre. The virus was isolated and identified in 1999.[2] The disease is named after a village in Malaysia,Sungai Nipah. Pigs may also be infected, millions of which were culled by Malaysian authorities in 1999 to successfully stop the spread of the disease.[2][9]
Human infections range from asymptomatic infection to acute respiratory infection, seizures and fatalencephalitis. This illness typically initially presents as 3-14 days of fever and headache, often accompanied by a cough, sore throat, difficulty breathing, and other signs of respiratory illness.[1] Infected people initially develop symptoms that include fever, headaches,myalgia, vomiting and sore throat. This can be followed by dizziness, drowsiness, altered consciousness, and neurological signs that indicate acute encephalitis. Some people can also experience atypical pneumonia and severe respiratory problems, including acute respiratory distress. Encephalitis and seizures occur in severe cases, progressing to coma within 24 to 48 hours.[1]
The incubation period is from 4 to 14 days but an incubation period as long as 45 days has been reported.[1]
Death occurs in 40-75% of cases, and some long-term side effects of infection include persistent convulsions and personality changes. Most survivors make a full recovery, although some are left with residual neurological conditions after acute encephalitis. Some cases of relapse have been reported.[1]
The initial case in human outbreaks of Nipah virus has always beenzoonotic[8] from exposure to contaminated secretions or tissues of infectedbats orpigs. Subsequent human-to-human transmission of Nipah virus occurs via close contact with NiV-infected persons or exposure to NiV-infected body fluids (e.g., blood, urine, nasal secretions).[1]
Most experts do not classify Nipah virus as airborne, though there is consensus that transmission can—and does—occur from short-range exposure to NiV-infected respiratory droplets in close contact settings.[10]
Indirect transmission of Nipah virus via contaminatedfomites is likely responsible for many cases in which there was no known direct contact with a NiV-infected person or animal.[1]
The risk of exposure is high for hospital workers and caretakers of those infected with the virus. In Malaysia and Singapore, Nipah virus infected people with close contact to infected pigs. In Bangladesh and India, the disease has been linked to consumption of raw date palm sap (toddy), eating of fruits partially consumed by bats, and using water from wells inhabited by bats.[11][12]
After recovery,IgG andIgM antibody detection can confirm a prior Nipah virus infection.Immunohistochemistry on tissues collected during autopsy also confirms the disease.[1]
Prevention through sanitary practices is the best protection. The likelihood of infection through animal transmission can be reduced by avoiding exposure to sick pigs, and to bats where the disease is endemic. Bats harbor a significantly higher proportion of zoonotic viruses than all other mammalian orders,[14] and are known not to be affected by the many viruses they carry, apparently due to their developing special immune systems to deal with the stress of flying.[15] Infection via bats can be caused by drinking raw palm sap (palm toddy) contaminated by bat excreta,[16] eating fruits partially consumed by bats, and using water from wells infested by bats.[12] Bats are known to drink toddy that is collected in open containers, and occasionally urinate in it, which contaminates it with the virus.[16]
Standard infection control practices can protect against human-to-humanhospital-acquired infections.[1] These include isolating patients, usingpersonal protective equipment (PPE), and maintaining strict hand hygiene practices. Individuals identified through contact tracing are tested and monitored until confirmed negative. Healthcare facilities must enforce rigorous infection prevention protocols when caring for suspected or confirmed cases.[17]
In January 2024 a candidate vaccine, ChAdOx1 NipahB, commencedPhase I clinical trials after completing laboratory and animal testing.[18][19]
As of 2020[update], there is no specific treatment for Nipah virus infection.[20] The mainstay of treatment issupportive care. While tentative evidence supports the use ofribavirin, it has not yet been studied in people with the disease.[1] Specific antibodies have also been studied in an animal model with potential benefit.[1]Acyclovir,favipiravir,[20] andremdesivir[21] have been assessed as potential antivirals against Nipah virus.
M 102.4 is a nonpatented monoclonal antibody developed by Christopher C. Broder, a professor of immunology and microbiology atUniformed Services University of the Health Sciences in Maryland. It proved highly effective in animal models. 50 doses were sent to Kerala in 2018, but it is not clear if they were used in humans.[citation needed]
Those who survive the initial infection often struggle with debilitating long-term neurologicalsequelae, includingmemory loss, impaired cognition,seizures,convulsions, and personality changes.[1]
Moreover, Nipah virus is known to be able topersist and lie dormant in survivors and to re-activate many months or years after the initial infection.[1] Deaths from re-activation of latent Nipah virus have been reported.[23]
Map showing locations of outbreaks of Nipah and Hendra virus as well as the range ofPteropus bats as of 2014
Nipah virus outbreaks have been reported in Malaysia, Singapore, Bangladesh and India. The area is known as the Nipah Belt. The highest mortality due to Nipah virus infection was found in Bangladesh,[citation needed] where outbreaks are typically seen in winter.[24] Nipah viruswas first seen in 1998 in peninsular Malaysia in pigs and pig farmers. By mid-1999, more than 265 human cases of encephalitis, including 105 deaths, had been reported in Malaysia, and 11 cases of either encephalitis or respiratory illness with one fatality were reported in Singapore.[25] In 2001, Nipah virus was reported fromMeherpur District, Bangladesh[26][27] andSiliguri, India.[26] The outbreak again appeared in 2003, 2004 and 2005 inNaogaon District,Manikganj District,Rajbari District,Faridpur District andTangail District.[27] In Bangladesh there were further outbreaks in subsequent years.[28][6]
2001: 31 January – 23 February,Siliguri, India: 66 cases with a 74% mortality rate.[30] 75% of patients were either hospital staff or had visited one of the other patients in hospital, indicating person-to-person transmission.
2001: April–May,Meherpur District, Bangladesh: 13 cases with nine fatalities (69% mortality).[31]
2004: 19 February – 16 April,Faridpur District, Bangladesh: 36 cases with 27 fatalities (75% mortality). 92% of cases involved close contact with at least one other person infected with Nipah virus. Two cases involved a single short exposure to an ill patient, including a rickshaw driver who transported a patient to hospital. In addition, at least six cases involved acute respiratory distress syndrome, which has not been reported previously for Nipah virus illness in humans.
2005: January,Tangail District, Bangladesh: 12 cases with 11 fatalities (92% mortality). The virus was probably contracted from drinking date palm juice contaminated by fruit bat droppings or saliva.[32]
2007: February–May,Nadia District, India: up to 50 suspected cases with 3–5 fatalities. The outbreak site borders the Bangladesh district ofKushtia where eight cases of Nipah virus encephalitis with five fatalities occurred during March and April 2007. This was preceded by an outbreak inThakurgaon during January and February affecting seven people with three deaths.[33] All three outbreaks showed evidence of person-to-person transmission.
2008: February–March, Manikganj and Rajbari districts, Bangladesh: Nine cases with eight fatalities.[34]
2010: January, Bhanga subdistrict, Faridpur, Bangladesh: Eight cases with seven fatalities. During March, one physician of the Faridpur Medical College Hospital caring for confirmed Nipah cases died.[35]
2011: February: An outbreak of Nipah Virus occurred at Hatibandha, Lalmonirhat, Bangladesh. The deaths of 21 schoolchildren due to Nipah virus infection were recorded on 4 February 2011.IEDCR confirmed the infection was due to this virus.[36] Local schools were closed for one week to prevent the spread of the virus. People were also requested to avoid consumption of uncooked fruits and fruit products. Such foods, contaminated with urine or saliva from infected fruit bats, were the most likely source of this outbreak.[37]
2018: May: Deaths of twenty one[38] people inPerambra nearCalicut,Kerala, India were confirmed to be due to the virus. Treatment using antivirals such as Ribavirin was initiated.[39][40]
2019: June: A 23-year-old student was admitted into hospital with Nipah virus infection atKochi in Kerala.[41] Health Minister of KeralaK. K. Shailaja said that 86 people who had had recent interactions with the patient were under observation. This included two nurses who treated the patient, and had fever and sore throat. The situation was monitored and precautionary steps were taken to control the spread of virus by theCentral[42] andState Government.[41] The Health Department of Kerala kept 338 people under observation, 17 of them in isolation. After undergoing treatment for 54 days at a private hospital, the 23-year-old student was discharged. On 23 July, the Kerala government declared Ernakulam district to be Nipah-free.[43]
2021: September: 12-year-old boy, a native ofChathamangalam village was admitted to a hospital atKozhikode in Kerala on September 1.[44] He died from the virus four days after admission.[45][46][47] Two healthcare workers who came into contact with the victim were already showing symptoms of Nipah infection by Monday.[48]
2023: Since 4 January 2023 and as of 13 February 2023, 11 cases (10 confirmed and one probable) including eight deaths (Case Fatality Rate (CFR) 73%) have been reported in Bangladesh. WHO assesses the ongoing risk as high at the national level.[49]
2023: September:Kozhikode district,Kerala, India: As of 14 September 2023, five cases, including two deaths, were confirmed in Kozhikode district in Kerala. The government has prepared a contact list of over 700 people linked to the two deaths, of whom two family members and a healthcare worker tested positive for the virus.[50][51]
2024 : July: One person died and 60 were identified as at risk of infection in Malappuram district,Kerala,India.[52][53]
Ribavirin has been studied in a small number of people. As of 2011[update], it was unclear whether it was useful, although a few people had returned to normal life after treatment.[55]In vitro studies and animal studies have shown conflicting results in the efficacy of ribavirin against NiV and Hendra, with some studies showing effective inhibition of viral replication in cell lines,[56][57] whereas some studies in animal models showed that ribavirin treatment only delayed but did not prevent death after NiV or Hendra virus infection.[58][59]
In 2013, the anti-malarial drugchloroquine was shown to block the critical functions needed for maturation of Nipah virus, although no clinical benefit was observed.[4]
Passive immunization using a human monoclonal antibody, m102.4, that targets the ephrin-B2 and ephrin-B3 receptor-binding domain of the henipavirus Nipah G glycoprotein was evaluated in the ferret model as post-exposure prophylaxis.[4][1] m102.4 has been used in people on acompassionate use basis in Australia, and was in pre-clinical development in 2013.[4]
^abcdefghijklmnopqrstuv"Nipah Virus (NiV)".Centers for Disease Control and Prevention, National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Division of High-Consequence Pathogens and Pathology (DHCPP), Viral Special Pathogens Branch (VSPB). 19 October 2022. Retrieved17 September 2023.
^abLooi LM, Chua KB (2007)."Lessons from the Nipah virus outbreak in Malaysia"(PDF).The Malaysian Journal of Pathology.29 (2). Department of Pathology, University of Malaya and National Public Health Laboratory of the Ministry of Health, Malaysia:63–7.PMID19108397.Archived(PDF) from the original on 30 August 2019.
^Wright PJ, Crameri G, Eaton BT (March 2005). "RNA synthesis during infection by Hendra virus: an examination by quantitative real-time PCR of RNA accumulation, the effect of ribavirin and the attenuation of transcription".Archives of Virology.150 (3):521–32.doi:10.1007/s00705-004-0417-5.PMID15526144.S2CID23885676.
![How the Nipah virus spreads[13]](/mt/?noimg=&dark=on&url=http%3a%2f%2fwww.wikipedia.org%2fwiki%2fFile%3aHow_the_Nipah_Virus_spreads.png)
