Sero- Epidemiological trends of Dengue Fever in Jammu Province of J&K State

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Available online at www.ijmrhs.com ISSN No: 2319-5886 International Journal of Medical Research & Health Sciences, 2016, 5, 8:1-6 Sero- Epidemiological trends of Dengue Fever in Jammu Province of J&K State Sudhan S Shashi 1, Sharma Monika 1, Gupta Rajiv Kumar 2 and Sambyal S Sorabh 1 1 Department of Microbiology, Govt. Medical College Jammu 2 Department of Community Medicine, Govt.Medical College Jammu ABSTRACT Dengue, an arthropod-borne arboviral disease is becoming a major public health concern, both in the tropical and subtropical regions of the world. In view of exponential increase in dengue positive cases reported in 2013, this study to follow the emerging trends of the disease over a period of five years from 2011 to 2015 was planned. The laboratory records of clinically suspected Dengue patients from 2011 to 2015 were analyzed retrospectively for the results of IgM anti dengue antibodies tested by Dengue IgM capture ELISA (MAC ELISA) along with demographic features, and seasonal variations. A total of five thousand nine hundred fifty (5950) samples from patients suspected of dengue infection were received and screened for the presence of dengue specific IgM antibodies.1891/5950 (31.78%)of the samples were found to be positive. The association between serum samples and different age groups was found to be highly significant (p=0.0000).dengue infection has recently become an endemic disease in this region occurring annually. In absence of specific treatment and vaccine for dengue fever (DF), early diagnosis is important in management of infection. This also demands continuous seroepidemiological surveillance for the timely formulation and implementation of effective dengue control programme. Moreover, serological crossreactivity with other Flaviviruses was unexpected in Jammu, for their absence. Key words: Seroepidemiology, Dengue fever, IgM antibody capture enzyme linked immune sorbent assay(mac ELISA), India, Vector. INTRODUCTION Dengue virus (DV) is a positive-stranded encapsulated RNA virus of the family Flaviviridae. There are four serotypes of the virus referred to as DV-1, DV-2, DV-3 and DV-4[1]. It is transmitted mainly by Aedes aegypti mosquito and also by Aedes albopictus. All four serotypes can cause the full spectrum of clinical illness, ranging from an asymptomatic or mild febrile illness to classic dengue fever (DF) to the most severe type of illness i.e. Dengue Hemorrhagic Fever (DHF) &Dengue Shock Syndrome (DSS) [2]. Global epidemiology of dengue is showing a discernible upward trend in recent years and the disease is associated with increasing frequency of outbreaks. In India first epidemic was experienced in Kolkata during1963-64. Since then DV infection has occurred in many places in India [3, 4]. One of the largest outbreaks in North India occurred in Delhi in 1996, followed by another in 2003[5]. The South East Asia region is currently experiencing an upsurge in reported cases of dengue in a number of countries, including India, Sri Lanka and Thailand [6]. Approximately 2.5 billion people are estimated to be at risk of acquiring dengue infection and 50 to 100 million people are believed to be infected worldwide annually, with half a million life-threatening infections requiring hospitalization, resulting in approximately 12,500 to 25,000 deaths (6).Treated DHF/DSS is associated with 3% mortality, while untreated is with 50 % mortality [7]. Thus, early laboratory diagnosis of dengue virus infection is important for management of the cases and is routinely done by serological tests. This study was designed to observe the trends of the serologically positive cases of dengue infection at Jammu, a town of North India from July to December over the period of five years from 2011-2015. 1

MATERIALS AND METHODS Before the start of this study permission was taken from the Institutional Ethical Committee (IEC), Government Medical College Jammu. In our study, blood samples were received from the various district hospitals and also from out-patient department and wards of medicine and paediatrics specialties of Govt. Medical College, Hospital, Jammu, a tertiary care teaching hospital and processing of samples was done at Department of Microbiology, GMC, Jammu. Cases with high fever and clinical symptoms suggestive of dengue infection (as per WHO criteria) were included in the study. 2 to 3 ml of blood was collected from each patient by nursing personnel or physicians using strict aseptic precautions and serum was collected using standard methods. Serum collected was tested for IgM anti dengue antibodies by Dengue IgM capture enzyme linked immune sorbent assay (MAC ELISA)(PanbioPty limited, Queensland, Australia or kits by National Institute of Virology, Pune). Briefly, the procedure was done as follows: 125 µl of peroxidase-labelled antidengue monoclonal antibody conjugate was added in the microwell containing dengue 1 to 4 antigens (antigen plate), resulting in the formation of antigen antibody complex. Within 10 min of addition of conjugate to the antigen plate, 100 µl of 1:100 diluted serum and control were added to another plate (assay plate) containing antihuman IgM antibodies or IgM antibodies attached to microwell test strips. The assay plate was incubated at 37 C for one hour and then washed. After that, 100 µl of complexed antigen conjugate solution was transferred from the antigen plate to assay plate which was further incubated for one hour. After incubation, the microwells were washed and 100 µl of tetramethyl-benzidine/ hydrogen peroxide (TMB/H 20 2 ) substrate solution was added to each well. After 10 min of incubation at room temperature, stop solution was added to each well and the colour density of the residue (optical density) was read within 30 min at the wavelength of 450 nm. Patients with positive anti dengue IgM were considered positive cases for dengue viral infection. For the year 2015, depending upon the duration of illness diagnosis of DV infection was done by demonstration of NS1Antigen (fever <5 days) or anti DV IgM antibodies (fever =/>5 days).the data was collected, tabulated and analysed. Pearson s chi-square test was used as test of significance and p<0.05 was considered significant. RESULTS The results have revealed that during five years of the study period, a total of 5950 serum samples were examined. It was further found that 1891/5950 samples were positive for IgM antibodies thus giving a positivity rate of 31.78%. The seasonal trend of the dengue fever for the month of July to December in the successive years of 2011-2015 is shown in Table-1. The state of Jammu and Kashmir has two provinces for administrative purposes, Jammu and Kashmir. Jammu province has ten districts under its jurisdiction and district wise distribution of serum samples is depicted in Table- 2. Sex wise distribution of the serum samples is shown in the Table- 3 and no association was found between sex and year of serum sample collection (p>0.05). The serum samples were further analyzed on the basis of age where it was found that 87.6% (1657/1891) of the serum samples belonged to age group 12years. This association between yearly serum samples and different age groups was found to be highly significant (p=0.0000). DISCUSSION Dengue is one of the most important emerging public health care problem of tropical and sub tropical region and in the last decade, a regular occurrence with periodic upsurges has been noted [8] in most parts of India. In our study, an increase in number of dengue patients has been observed in year 2013 and 2015. Maximum seropositivity was reported in the year 2013 i.e.36% followed by 16.9% in the year 2015. The dengue positive cases were seen to be on the lower side in the year 2011,2012 and 2014 as only few cases were reported i.e., 4.5%,3.5%and 1.29% respectively. In the current study, 31.78% samples were serologically positive for dengue infection while Ekta etal reported a slightly higher rate of 44.56% of seropositivity in their study. Other studies associated in India from Delhi and Gwalior reported much higher seropositivity rates to the tune of 95%, and 65% respectively [9, 10]. However the results of present study are in agreement with a study from Brazil, which also reported a seropositivity of 30% [11]. The higher seropositivity in other studies could be best explained because of the heavy load of migratory floating population from dengue endemic states of India and higher dengue virus activity resulting into higher rate of transmission. Another factor which could contribute to higher rates of transmission could be temporary shelters for 2

construction workers who do not have adequate water supply and are forced to store water for construction as well for human use which could act as breeding grounds for the mosquitoes. However, dengue was hypoendemic in the Jammu province despite the fact that the climate of Jammu is favourable for growth and spread of virus. Three plain districts of Jammu province Kathua, Samba and Jammu, adjoin the state of Punjab and climate is similar in both the regions. District wise distribution of seropositive samples show a clear trend of more number of cases from these three districts in comparison to the rest of districts of Jammu province which usually have a hilly terrain. Dengue infection is no more an urban area infection but it has affected the rural areas also as positive samples were found to be present in patients residing in rural areas also. Human migration patterns disperse vectors and viruses in the new areas. Further, the rise found in the year 2013 may be partially attributed to the rapid unplanned urbanization with unchecked construction activities and poor sanitation facilities contributing fertile breeding grounds for mosquitoes. It is also true that an increase in the alertness among medical fraternity following the initial epidemics in North India and the availability of diagnostic tools in the hospital have contributed to the increased detection of cases. A monthly distribution of the cases in the current study shows an increase from the month of September onwards which concurs with other outbreaks in India [12]. To correlate the seasonal variation of the disease, analysis of the data on monthly basis was done. A gradual increase in cases was noticed from August with a peak in October, during the study. The correlation between occurrence of dengue and monsoon season is clearly evident in this study and is further supported by similar findings from Delhi, Ludhiana, Chandigarh and Karachi [12-15]. It may be because this season is very favorable for high breeding of the vector, that is, Aedes aegypti. This seasonal outbreak of disease transmission is very important at local level for effective control measures and that preventive measures against dengue infection should come into full swing during water stagnation periods after the initial bouts of rainfall and at the end of monsoon. Fig 1.Distribution of positive and total serum samples on an yearly basis 6000 5000 4000 3000 Positive patients Total no. of Patients 2000 1000 0 2015 2014 2013 2012 2011 Table1: Year and month-wise Distribution of the collected samples from 2011-2015 Year July Aug Sept Oct Nov Dec Total 2015 0(1) 3(37) 26(166) 80(339) 8(127) 0(22) 117 (692) 2014 0(5) 0(15) 0(26) 0(18) 1(11) 0(2) 1(77) 2013-0(16) 213(766) 1186(3668) 109(680) 7(29) 1762(4891) 2012 0(8) 0(41) 2(70) 4(47) 1(34) 0(0) 7(200) 2011 0(0) 0 0 0(18) 4(42) 0(29) 4(90). 3

Table2: District-wise distribution of dengue cases in Jammu Province Year Jammu Samba Kathua Udhampur Reasi Poonch Ramban Rajouri Doda Kishthwar 2015 77(474) 7(36) 20(84) 2(26) 3(18) 1(8) 1(6) 2(20) 3(18) 1(2) 117(692) 2014 1 (77) - - - - - - - - - 1 (77) 2013 1265 405 56(190) 8(33) 6(22) 5(10) 6(13) 9(15) 2(15) 0(5) 1762(4891) (3387) (1201) 2012 7(200) - - - - - - - - - 7(200) 2011 4(90) - - - - - - - - - 4(90) Table 3: Year & Sex-wise distribution of dengue cases Year Male Female Total 2015 90 (469) 27 (223) 117(692) 2014 1(43) 0(34) 1(77) 2013 1350( 3160) 412 (1731) 1762(4891) 2012 4(116) 3(76) 7(200) 2011 2(55) 1(35) 4(90) Chi-square (x 2 ) = 1.952 Df = 4 p = 0.7445 Fig.2 Distribution of cases on the basis of sex sex-wise distribution of dengue cases Male Female Table 4: Distribution of the dengue Positive cases on the basis of age& year Chi-square (x 2 ) = 37.02 Df = 4 p = 0.0000 Year 0 <12yrs 12 and above Total 2015 35 82 117(692) 2014 0 1 1(77) 2013 198 1564 1762(4891) 2012 0 7(200) 7(200) 2011 1(3) 3(87) 4(90) Sex wise analysis revealed a male predominance, which is consistent with observations in other Indian studies [16, 17]. Males are associated with more outdoor activities leading to increased proneness to mosquito bite during the day time. Our study revealed that only 12.37% (234 /1864) children below the age of 12 years were found to be positive and majority of the cases were present in age group beyond 12 years. These findings are consistent 4

with other Indian studies, as most of the other Indian studies have reported 12 to 45 years as the most affected age group [16-18]. On the contrary, several international studies, dengue has been reported to mainly a pediatric public health problem for example a study from Cambodia further reported large number of pediatrics admission for dengue fever in a National Pediatric Hospital [19]. The main limitation of the current study was that all the serum samples were collected from the government hospitals / institutions.so, the patients going to private hospitals or private practioners could not be included in the study for the obvious reasons. Thus it would be pertinent to admit that the trends of dengue fever in this study may not be truly representative of the Jammu province. CONCLUSION Dengue continues to be a global challenge as public health problem, both in underdeveloped and developing countries. There is no available antiviral therapy and management is mainly supportive. Early detection of DF can help to reduce morbidity and mortality especially in DHF and DSS cases. Thus, tests to detect NS1 antigen and IgM antibodies should be available at primary health centers, so that cases can be diagnosed early and thus properly managed. Also, implementation of vector control strategies is essential to prevent such outbreaks. This will also be beneficial in controlling the other mosquito borne diseases like Chikungunya, Japanese Encephalitis, West Nile, Zika, Yellow Fever encephalitis etc and even the vector borne parasitic disease like Malaria and Filaria. REFERENCES [1] Gubler DsJ. Dengue and Dengue haemorrhagic fever. Clin Microbiol Rev.1998; 11: 480-96. [2] Martina BE, Koraka P, Osterhaus A. Dengue virus pathogenesis,an integrated view. ClinMicrobiol Rev. 2009; 22:564 581. [3] Ekta Gupta, Lalit Dar, Geetanjali Kapoor, ShobhaBroor. The changing epidemiology of dengue in Delhi, India Virol J. 2006; 3: 92. [4] Dar L, Broor S, Sengupta S, Xess I, Seth P: The first major outbreak of dengue hemorrhagic fever in Delhi, India. Emerg Infect Dis. 1999; 5:589-90. [5] Chaturvedi UC, Shrivastava R. Dengue Haemorrhagic Fever. Ind J Med Microbiol. 2004; 22(1):5-6. [6] Dengue in South East Asian Region 2010. A report by World Health Organization, available on website www.who.com; accessed on 25.2.2010. [7] Monath TP. Dengue: the risk to developed and developing countries. Proc Nat Acad Sci.1994; 91: 2395-2400. [8] Singh B. Dengue outbreak in 2006: Failure of public health system? Indian J. Community Med. 2007; 32: 99-100. [9] Parida MM, Dash PK, Upadhyay C, Saxena P, Jana AM. Serological and virological investigation of an Outbreak of Dengue fever in Gwalior, India. Indian J Med Res. 2002; 116: 248-254. [10] Kurukumbi M, Wali JP, Broor S, Aggarwal P, Seth P, Handa R et al. Seroepidemiology and active surveillance of dengue fever / dengue hemorrhagic fever in Delhi. Indian J Med Sci.2001; 55(3): 149-156. [11] Reiter P, Lathrop S, Bunning M, Singer D, Tiwari T et al. Texas lifestyle limits transmission of dengue fever. Emerg Infect Dis. 2003; 9:1-7. [12] Gupta Ekta, Dar L, Narang P, Srivatava VK, Barror S. Serodiagnosis of dengue during an outbreak at a tertiary hospital in Delhi. Indian J Med Res. 2005; 121:36-38. [13] Lal M, aggarwal A, Oberoi M. Dengue fever, an emerging viral problem in Ludhiana, North India. Ind. Jr. Community Med. 2007; 51: 198-199. [14] Ratho RK, Mishra B, Kaur J, Kakkar N, Sharma K. An outbreak of dengue fever in PeriUrban slums of Chandigarh, India, with special reference to entomological and climatic factors. Indian J. Med. Sci. 2005; 59: 519-27. [15] Ahmed S, Arif F, Yahya Y, Rehman A, Abbas K, Ashraf S et al. Dengue fever outbreak in Karachi 2006 - A study of profile and outcome of children under 15 years of age. J Pakistan Med Assoc. 2008; 58: 4-8. [16] Ukey PM, Bondade SA, Paunipagar PV, Powar RM, Akulwar SL. Study of seroprevalence of dengue fever in central India. Indian J.Comm. Med. 2010; 35: 517-9 [17] Gupta E, Dar L, Narang P, Srivastava VK, Broor S. Serodiagnosis of dengue during an outbreak at a tertiary care hospital in Delhi. Indian J. Med. Res. 2005; 121: 36-8. [18] Kumar A, Rao R, Pandit V, Shetty s, BamigattiC,Samaraging CM Clinical manifestation and trend of dengue cases admitted in tertiary care hospital, Udupi, Karnataka. Ind. Jr. Comm. Med. 2010; 35:386-391. 5

[19] Y.MengChour, Gaye Ruble, Rathsvuth Hong, Kyi MinnYuvathakdan, Touch Sok et al. Hospital.based diagnosis of hemorrhagic fever,encephalitis, and hepatitis in Cambodian children. Center for Disease control and prevention. 2002; 8: 1-7. 6