|
|
REVIEW |
|
Year : 2012 | Volume
: 1
| Issue : 2 | Page : 208-212 |
|
Nipah virus outbreaks in Bangladesh: a deadly infectious disease
Mahmudur Rahman, Apurba Chakraborty
Institute of Epidemiology, Disease Control and Research, Mohakhali, Dhaka-1212, Bangladesh
Date of Web Publication | 24-May-2017 |
Correspondence Address: Mahmudur Rahman Institute of Epidemiology, Disease Control and Research, Mohakhali, Dhaka-1212 Bangladesh
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/2224-3151.206933
During 2001-2011, multidisciplinary teams from the Institute of Epidemiology, Disease Control and Research (IEDCR) and International Centre for Diarrhoeal Disease Research, Bangladesh(icddr,b) identified sporadic cases and 11 outbreaks of Nipah encephalitis. Three outbreaks were detected through sentinel surveillance; others were identified through event-based surveillance. A total of 196 cases of Nipah encephalitis, in outbreaks, clusters and as isolated cases were detected from 20 districts of Bangladesh; out of them 150 (77%) cases died. Drinking raw date palm sap and contact with a case were identified as the major risk factors for acquiring the disease. Combination of surveillance systems and multidisciplinary outbreak investigations can be an effective strategy not only for detection of emerging infectious diseases but also for identification of novel characteristics and risk factors for these diseases in resource-poor settings.
Keywords: Nipah virus, outbreak, surveillance, transmission, communicable disease, Bangladesh.
How to cite this article: Rahman M, Chakraborty A. Nipah virus outbreaks in Bangladesh: a deadly infectious disease. WHO South-East Asia J Public Health 2012;1:208-12 |
Introduction | |  |
Nipah is a recently detected viral zoonotic disease caused by Nipah virus originating from a new genus -the Henipa virus.[1],[2] Pteropus bats are the zoonotic host of the virus and pigs are the likely amplifying host.[2],[3] The virus was first identified in Nipah village of Malaysia in 1998,[2],[4] since then three other countries have reported human cases of Nipah virus infection, including Bangladesh.[5],[6],[7] The Institute of Epidemiology, Disease Control and Research (IEDCR), a government mandated institute, conducted disease surveillance and outbreak investigations for Nipah encephalitis in Bangladesh. We present a review of the methods used for detecting these cases and their novel characteristics and risk factors through outbreak investigations during 2001-2011.
Methods | |  |
We reviewed IEDCR strategies and guidelines from its records to explore the mechanism for detection of Nipah cases and clusters. We also reviewed the method of hospital-based Nipah surveillance jointly conducted by IEDCR and the International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b). Outbreak investigation reports were studied to identify the sources of information through which these outbreaks were detected. The Nipah surveillance database was used to describe the demographic and clinical characteristics of the identified Nipah cases. Published reports on Nipah encephalitis in Bangladesh and unpublished outbreak investigation reports were reviewed to identify the risk factors for Nipah encephalitis in Bangladesh.
Results | |  |
To detect disease outbreaks, IEDCR conducts both ‘event-based surveillance’ and ‘surveillance for specific disease or conditions’. Up to April 2010, as part of the event-based surveillance, IEDCR conducted unstructured monitoring of newspapers and television channels for reports of suspected disease outbreaks. In April 2010, IEDCR started a more structured surveillance of suspected disease outbreak reports in 10 national newspapers and eight national television channels. Any reported cluster or outbreak of known illness and even report of a single death from unknown disease is captured through this surveillance method. In addition to the media surveillance, IEDCR has two hotline numbers for healthcare providers to report disease outbreaks. Through district and sub-district rapid response teams, IEDCR verifies the existence of any outbreak and conducts investigation.
To identify outbreaks of encephalitis through enhanced surveillance networks and to identify risk factors for transmission of Nipah encephalitis, IEDCR in collaboration with the International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b) has been conducting surveillance for Nipah encephalitis in Bangladesh since 2006. Initially, this surveillance programme started in 10 hospitals. Currently, the surveillance is functioning in five hospitals in northwestern and central Bangladesh. Clinicians of sentinel hospitals identify and list all encephalitis cases presenting in the surveillance hospitals. A case of encephalitis is defined as any person with history of acute onset of fever or axillary temperature of >38.5°C and evidence of acute brain pathology manifested by altered mental status or new onset of seizure or neurological deficit. Any cluster of encephalitis cases, defined by two encephalitis cases within 21 days of each other and within half an hour walking distance from each other, identified through the sentinel hospitals are investigated by a trained team of epidemiologists from IEDCR and icddr,b.
As part of the cluster investigation the IEDCR and icddr,b team conducts search for encephalitis cases in the community adjacent to the cluster and carries out epidemiological research to identify risk factors. In case of outbreaks of encephalitis that are detected through event-based surveillance or sentinel surveillance, a team of epidemiologists, veterinarians and anthropologists conduct outbreak investigations. These investigations include identification of alive or deceased human cases suspected of having Nipah encepahlitis, identification of possible animal sources of the infection, assessment of environmental contamination, and study of possible behavioural factors contributing to the outbreak and case control study to identify possible risk factors. For each case of Nipah encephalitis, four age-matched neighbourhood controls are selected for case control study. Exposure histories of both cases and controls within 30 days prior to the onset of illness are collected.
In case of any encephalitis cluster or outbreak, investigation teams collect blood from the suspected encephalitis cases and samples are sent to IEDCR. Initially, samples were sent to Centers for Disease Control and Prevention, USA (CDC) for testing. Later in 2007, a Nipah laboratory was set up at IEDCR for safe specimen handling and testing. Virologists of IEDCR conduct enzyme-linked immunosorbent assay to identify IgM and IgG antibodies against Nipah virus.
In Bangladesh, Nipah outbreak was first confirmed in 2003, when a team from Centers for Disease Control and Prevention, Atlanta, USA (CDC), icddr,b and the Government of Bangladesh retrospectively investigated two outbreaks of suspected encephalitis with human deaths which had occurred in Meherpur district in 2001 and in Naogaon in 2003.[7] Including these two, 11 outbreaks of Nipah encephalitis have been detected in Bangladesh since 2001. Five of these outbreaks were detected from newspaper reports of human deaths from unknown illness, three were reported by sentinel hospitals, one was reported from a private hospital and others were reported by the civil surgeon of a district. During this period, 196 cases of Nipah encephalitis were detected from 20 districts of Bangladesh in outbreaks, clusters and as isolated cases; out of these 150 (77%) cases died.
The Nipah cases were mostly distributed in the northwestern and central part of Bangladesh. Outbreaks occurred during December to May, which coincides with the winter season in Bangladesh. Cases were distributed in all age groups. Median age was 25 years (range: 0.5-75 years) and 124 (63%) cases were males. Median duration from onset of illness to death was six days (range: 1-47 days). In the course of illness, 123 (63%) Nipah encephalitis cases developed acute respiratory distress syndrome [Table 1].
Drinking raw date palm sap collected during winter months, which is a delicacy in rural Bangladesh, was first identified as a risk factor for Nipah infection in an outbreak in Tangail in 2005.[8] This has also been identified as a risk factor in three more outbreaks so far. Several sporadic cases have also reported history of drinking raw date palm sap within 30 days before the onset of illness. Close contacts with a sick person or his/her secretions and contact with sick animals were the other two risk factors identified through case control studies in different outbreak investigations [Table 2]. | Table 2: Risk factors identified through case control studies in Nipah outbreaks of Bangladesh
Click here to view |
Pteropus bats were found to be positive for Nipah antibodies in different outbreak areas.[7] A zoonotic investigation team of icddr,b identified the way bats contaminate the shaved surface of the date palm trees (from where the sap is collected) using infrared camera.[9]
Discussion | |  |
A combination of an ‘event-based’ and ‘sentinel’ surveillance system has been a successful strategy in Bangladesh for detecting recurrent outbreaks of Nipah encephalitis. Multidisciplinary collaborative investigation of the outbreaks identified the clinical characteristics, risk factors and mode of transmission of this highly fatal zoonotic disease.
Over 50 species of Pteropus bats, the natural reservoir of Nipah virus, live in South and South-East Asian countries.[10] After the large outbreak of Nipah encephalitis in Malaysia, only three outbreaks have been reported from countries other than Bangladesh, one in Singapore and two in India.[5],[6] Therefore, it is important to know whether specific environmental or host factors are responsible for recurrent transmission of Nipah virus to humans in Bangladesh or whether virus detections are the result of an efficient surveillance system. Although Bangladesh, like many other low-income countries, lacks an integrated disease surveillance system, the combination of event-based surveillance system with a sentinel surveillance system for encephalitis has possibly increased the likelihood of identifying Nipah cases in Bangladesh in comparison to some other countries in the region, which lack a strong surveillance for encephalitis.
While more than 95% of the Nipah cases in Malaysia had a history of contact with pigs,[11] in only one of the 11 Bangladeshi outbreaks a close proximity to pig herds was identified as a risk factor. Identification of the drinking of raw date palm sap, a unique cultural practice in rural Bangladesh[12] and possibly in the neighbouring Indian states, as a risk factor for acquiring Nipah infection in Bangladesh and the validation of the plausibility of contamination of date palm sap with Nipah virus from Pteropus bats through separate zoonotic investigation highlights the importance of a multidisciplinary approach in investigating outbreaks of zoonotic diseases.[9]
Nipah outbreaks in Bangladesh have presented some features distinctly different than the outbreak in Malaysia. In Bangladesh, a higher proportion of Nipah cases suffered from respiratory symptoms than in Malaysia.[4] Also, the case fatality ratio was higher in Bangladesh, which may be related to the lack of access of Bangladeshi cases to intensive care facilities.[4] Like in other diseases caused by paramyxoviruses, such as measles, mumps, respiratory syncytial virus infection, parainfluenza, person-to-person transmission was a common mode of transmission in Bangladeshi Nipah cases, but this mode of transmission was not common in Nipah encephalitis cases in Malaysia. Therefore, future investigations should focus on exploring the reasons for variable presentation and different modes of transmission of Nipah virus in different settings.[16]
To conclude, Nipah encephalitis, a fatal zoonotic disease, recurrently claims lives in Bangladesh following the initial reports of outbreaks in other countries. A combination of event-based and sentinel surveillance systems is an innovative strategy to detect encephalitis outbreaks which has been successful in detecting Nipah outbreaks in Bangladesh. Multidisciplinary outbreak investigations can be an important tool in exploring novel characteristics and risk factors of emerging infectious zoonotic diseases in resource-poor settings.
References | |  |
1. | Chua KB. Nipah virus outbreak in Malaysia. J Clin Virol. 2003;26:265-75. |
2. | Chua KB, Bellini WJ, Rota PA, et al. Nipah virus: a recently emergent deadly paramyxovirus. Science. 2000;288:1432-5. |
3. | Epstein JH, Field HE, Luby S, Pulliam JR and Daszak P. Nipah virus: impact, origins, and causes of emergence. Curr Infect Dis Rep. 2006;8:59-65. |
4. | Goh KJ, Tan CT, Chew NK, et al. Clinical features of Nipah virus encephalitis among pig farmers in Malaysia. N Engl J Med. 2000;342:1229-35. |
5. | Paton NI, Leo YS, Zaki SR, et al. Outbreak of Nipah-virus infection among abattoir workers in Singapore. Lancet. 1999;354:1253-6. |
6. | Harit AK, Ichhpujani RL, Gupta S, et al. Nipah/Hendra virus outbreak in Siliguri, West Bengal, India in 2001. Indian J Med Res. 2006;123:553-60. |
7. | Hsu VP, Hossain MJ, Parashar UD, et al. Nipah virus encephalitis reemergence, Bangladesh. Emerg Infect Dis. 2004;10:2082-7. |
8. | Luby SP, Rahman M, Hossain MJ, et al. Foodborne transmission of Nipah virus, Bangladesh. Emerg Infect Dis. 2006;12:1888-94. |
9. | Khan MS, Hossain J, Gurley ES, Nahar N, Sultana R and Luby SP. Use of infrared camera to understand bats’ access to date palm sap: implications for preventing Nipah virus transmission. Ecohealth. 2010;7:517-25. |
10. | Luby SP, Gurley ES and Hossain MJ. Transmission of human infection with Nipah virus. Clin Infect Dis. 2009;49:1743-8. |
11. | Parashar UD, Sunn LM, Ong F, et al. 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. J Infect Dis. 2000;181:1755-9. |
12. | Rahman MA, Hossain MJ, Sultana S, et al. Date Palm Sap Linked to Nipah Virus Outbreak in Bangladesh, 2008. Vector Borne Zoonotic Dis. 2012;12(1):65-72. |
13. | Montgomery JM, Hossain MJ, Gurley E, et al. Risk factors for Nipah virus encephalitis in Bangladesh. Emerg Infect Dis. 2008;14:1526-32. |
14. | Gurley ES, Montgomery JM, Hossain MJ, et al. Person-to-person transmission of Nipah virus in a Bangladeshi community. Emerg Infect Dis. 2007;13:1031-7. |
15. | Homaira N, Rahman M, Hossain MJ, et al. Cluster of Nipah virus infection, Kushtia District, Bangladesh, 2007. PLoS One. 2010;5:e13570. |
16. | Homaira N, Rahman M, Hossain MJ, et al. Nipah virus outbreak with person-to-person transmission in a district of Bangladesh, 2007. Epidemiol Infect; 138:1630-6. |
[Table 1], [Table 2]
This article has been cited by | 1 |
The Epidemiological Characteristics of the Korean Bat Paramyxovirus between 2016 and 2019 |
|
| Seong Sik Jang,Ji Yeong Noh,Van Thi Lo,Yong Gun Choi,Sun-Woo Yoon,Dae Gwin Jeong,Hye Kwon Kim | | Microorganisms. 2020; 8(6): 844 | | [Pubmed] | [DOI] | | 2 |
Nipah Virus: Past Outbreaks and Future Containment |
|
| Vinod Soman Pillai,Gayathri Krishna,Mohanan Valiya Veettil | | Viruses. 2020; 12(4): 465 | | [Pubmed] | [DOI] | | 3 |
Exploiting the Legacy of the Arbovirus Hunters |
|
| Nikos Vasilakis,Robert B. Tesh,Vsevolod L. Popov,Steve G. Widen,Thomas G. Wood,Naomi L. Forrester,Jean Paul Gonzalez,Jean Francois Saluzzo,Sergey Alkhovsky,Sai Kit Lam,John S. Mackenzie,Peter J. Walker | | Viruses. 2019; 11(5): 471 | | [Pubmed] | [DOI] | | 4 |
Case fatality rate and risk factors for Nipah virus encephalitis: A systematic review and meta-analysis |
|
| Sebastien Kenmoe,Maurice Demanou,Jean Joel Bigna,Cyprien Nde Kengne,Abdou Fatawou Modiyinji,Fredy Brice N. Simo,Sara Eyangoh,Serge Alain Sadeuh-Mba,Richard Njouom | | Journal of Clinical Virology. 2019; 117: 19 | | [Pubmed] | [DOI] | | 5 |
Nipah virus infection: A review |
|
| Pierre E. Aditi,M. Shariff | | Epidemiology and Infection. 2019; 147 | | [Pubmed] | [DOI] | | 6 |
Nipah virus: epidemiology, pathology, immunobiology and advances in diagnosis, vaccine designing and control strategies – a comprehensive review |
|
| Raj Kumar Singh,Kuldeep Dhama,Sandip Chakraborty,Ruchi Tiwari,Senthilkumar Natesan,Rekha Khandia,Ashok Munjal,Kranti Suresh Vora,Shyma K. Latheef,Kumaragurubaran Karthik,Yashpal Singh Malik,Rajendra Singh,Wanpen Chaicumpa,Devendra T. Mourya | | Veterinary Quarterly. 2019; 39(1): 26 | | [Pubmed] | [DOI] | | 7 |
Henipaviruses at the Interface Between Bats, Livestock and Human Population in Africa: A Review |
|
| Cyrille Mbanwi Mbuću,Wilfred Fon Mbacham,Pierre Gontao,Sylvain Leroy Sado Kamdem,Alexandre Michel Njan Nlôga,Martin H. Groschup,Abel Wade,Kerstin Fischer,Anne Balkema-Buschmann | | Vector-Borne and Zoonotic Diseases. 2019; | | [Pubmed] | [DOI] | | 8 |
Clinical Manifestations of Nipah Virus–Infected Patients Who Presented to the Emergency Department During an Outbreak in Kerala State in India, May 2018 |
|
| Radhakrishnan Chandni,T P Renjith,Arshad Fazal,Noufel Yoosef,C Ashhar,N K Thulaseedharan,K P Suraj,M K Sreejith,K G Sajeeth Kumar,V R Rajendran,A Remla Beevi,R L Sarita,Attayur P Sugunan,Govindakarnavar Arunkumar,D T Mourya,Manoj Murhekar | | Clinical Infectious Diseases. 2019; | | [Pubmed] | [DOI] | | 9 |
Infections among Contacts of Patients with Nipah Virus, India |
|
| C.P. Girish Kumar,Attayur P. Sugunan,Pragya Yadav,Karishma Krishna Kurup,Renjith Aarathee,Ponnaiah Manickam,Tarun Bhatnagar,Chandni Radhakrishnan,Beena Thomas,Akhilesh Kumar,Jayasree Jayasree,Beena Philomina,K.G. Sajeeth Kumar,N.K. Thulaseedharan,Nivedita Gupta,R. Rajendran,R.L. Saritha,Devendra T. Mourya,Raman R. Gangakhedkar,Manoj V. Murhekar | | Emerging Infectious Diseases. 2019; 25(5) | | [Pubmed] | [DOI] | | 10 |
Analysis of Nipah Virus Codon Usage and Adaptation to Hosts |
|
| Rekha Khandia,Shailja Singhal,Utsang Kumar,Afzal Ansari,Ruchi Tiwari,Kuldeep Dhama,Jayashankar Das,Ashok Munjal,Raj Kumar Singh | | Frontiers in Microbiology. 2019; 10 | | [Pubmed] | [DOI] | | 11 |
Controlling Nipah virus encephalitis in Bangladesh: Policy options |
|
| Jasmine Dhillon,Arinjay Banerjee | | Journal of Public Health Policy. 2015; 36(3): 270 | | [Pubmed] | [DOI] | |
|
 |
 |
|