Preliminary Seroepidemiological survey of dengue infections in Pakistan, 2009-2014
Infectious Diseases of Poverty volume 6, Article number: 48 (2017)
Dengue virus is the causative agent of dengue fever, a vector borne infection which causes self-limiting to life threatening disease in humans. A sero-epidemiological study was conducted to understand the current epidemiology of dengue virus in Pakistan which is now known as a dengue endemic country after its first reported outbreak in 1994.
To investigate the prevalence of dengue virus in Pakistan during 2009-2014, a total of 9,493 blood samples were screened for the detection of anti-dengue IgM antibodies using ELISA. Clinical and demographic features available with hospital records were reviewed to ascertain mortalities related to dengue hemorrhagic shock syndrome.
Out of 9,493 samples tested, 37% (3,504) were found positive for anti-dengue IgM antibodies. Of the seropositive cases, 73.6% (2,578/3,504) were male and 26.4% (926/3,504) were female. The highest number (382/929; 41.1%) of sero-positive cases was observed among the individuals of age group 31-40 years. The highest number of symptomatic cases was reported in October (46%; 4,400/9,493), and the highest number of sero-positive cases among symptomatic cases was observed in November (45.7%; 806/1,764). Mean annual patient incidence (MAPI) during 2009-2014 in Pakistan remained 0.30 with the highest annual patient incidence (11.03) found in Islamabad. According to the available medical case record, 472 dengue related deaths were reported during 2009-2014.
The data from earlier reports in Pakistan described the dengue virus incidence from limited areas of the country. Our findings are important considering the testing of clinical samples at a larger scale covering patients of vast geographical regions and warrants timely implementation of dengue vector surveillance and control programs.
Trial registration number
It is an epidemiological research study, so trial registration is not required.
Please see Additional file 1 for translations of the abstract into six official working languages of the United Nations.
Dengue virus belongs to the genus Flavivirus within the family Flaviviridae, and contains single stranded positive sense RNA genome. There are four serotypes of dengue virus DENV1-4 . The primary infection caused by a single DENV serotype is usually mild and self-limiting. The more severe form of dengue infection is dengue hemorrhagic fever (DHF) and dengue shock syndrome (DSS) responsible for high morbidity and mortality . Since the introduction of new dengue guidelines by World Health Organization (WHO) in 2009, dengue is classified into three clinical stages: dengue without warning signs; dengue with warning signs (abdominal pain, persistent vomiting, fluid accumulation, mucosal bleeding, lethargy, liver enlargement, increasing hematocrit with decreasing platelets) and severe dengue (dengue with severe plasma leakage, severe bleeding or organ failure) .
Mostly Dengue virus infection is characterized by high grade fever, headache, skin rash, muscle pain, joint pain, and retro-orbital pain etc . Typically, the secondary dengue infection with a different serotype than the primary infection is associated with severe clinical manifestations. Dengue virus is transmitted by mosquitoes mainly Aedes aegypti and to lesser extent by Aedes albopictus. The Ae. aegypti is a day biting mosquito and breeds in artificial as well as the natural water resources . According to WHO, more than 124 countries are at risk of dengue virus infection and more than 100 million cases of dengue virus infection with 25 000 estimated deaths are reported per annum globally .
Pakistan reported its first outbreak of dengue hemorrhagic fever in 1994 . With several subsequent outbreaks across country reported to date . For instance, during 2010–2011, dengue outbreak had occurred in many districts of Punjab province including Lahore, Sheikhupura, Gujranwala, Faisalabad, Attock and Rawalpindi followed by 2013–2014 outbreaks in Swat and Mansehra [9–19].
This study was approved by the Internal Review Board of National Institute of Health, (NIH) Islamabad, Pakistan.
This research study was conducted on the serum samples received at Department of Virology, NIH, Islamabad Pakistan from different hospitals across the country during January 2009-December 2014. The NIH Islamabad serves as the country’s epic public health institute and receives thousands of samples for diagnostic services and disease outbreak investigations from all over the country. Due to lack of an active surveillance system and poor diagnostic capacities for hemorrhagic fever infections, samples from suspected patients attending outpatient department and those hospitalized due to severe clinical signs and symptoms at country hospitals are referred to NIH for screening and confirmation.
Sample collection and laboratory diagnosis
A total of 9 493 acute phase blood samples were analyzed for the detection of anti-dengue IgM using capture Enzyme linked immunosorbent assay (Dengue IgM ELISA, Panbio Tech Co Brisbane, Australia). Five milliliters (ml) of blood sample was drawn from suspected dengue patients attending hospitals and transported to Department of Virology, NIH Islamabad. All blood samples were centrifuged at 3000 rpm for 5 min and serum was stored at −70 °C until further processing.
Assay procedure for the detection of anti-dengue IgM by ELISA
All serum samples were analyzed for the detection of anti-dengue IgM antibodies using IgM capture ELISA (Panbio Tech Co Brisbane, Australia) according to the instructions provided by the manufacturer. This kit is used for the qualitative detection of anti-dengue IgM antibodies in patients’ serum with reported sensitivity and specificity of 55.7–94.7% and 97–100%, respectively.
Briefly 96 well microtiter plate was precoated with anti-human IgM antibodies. 100 μl of diluted (1:100) serum sample and positive/negative controls were dispensed to the respective wells and plate was incubated at 37 °C for 1 h. During first incubation, anti-dengue IgM antibodies, if present in the patient’s serum sample were bound to anti human IgM antibodies. At the end of incubation, all wells were six times washed with wash buffer followed by addition of 100 μl diluted antigen to each well and plate was incubated at 37 °C for 1 h. During second incubation anti-dengue horse radish peroxidase conjugate was used followed by washing out the unbound antigen/antibody complex and addition of 100 μl of TMB (3, 3′, 5, 5′-Tetramethylbenzidine) substrate. The plate was finally incubated at 37 °C for 10 min. The reaction was then stopped and absorbance (optical density) was read within 30 min using as ELISA reader at a wavelength of 450 nm.
Interpretation of assay results
The results of test were interpreted by the calculating cut-off value which is the average absorbance of triplicate of calibrator multiplied with 0.62. Index value was calculated by dividing sample´s optical density (O.D) by the cut-off value. Panbio unit was calculated by multiplying the index value with 10. The final sample results were interpreted as follow.
Geographic distribution of dengue cases was determined based on the information provided on patient investigation forms. The seasonal incidence was determined by grouping all dengue cases into monthly intervals based on the time of disease onset. Medical history records of dengue cases available with the hospitals were also reviewed to collect the required data including dengue related deaths in Pakistan during 2009–2014. Data was collected from registers, patient investigation forms as well as a questionnaire was administered to obtain demographic and clinical information including the patient´s age, gender, clinical signs and symptoms, area of residence, date of admission, date of onset, travel history to dengue endemic areas, status at the time of discharge and prognosis.
The annual patient incidence (API) was calculated as the number of sero-positive (IgM+) patients per 100 000 inhabitants for each of the study sites in each year [API = (number of sero-positive patients/population) × 100 000]. Mean Annual Patient Incidence (MAPI) was calculated as- “the sum of each year’s API in the each study site divided by total study duration i.e.6 years [MAPI = (sum of 6 year’s API)/6].
Data was analyzed using Statistical Package for Social Science version 20 (SPSS v.20)
From January 2009 to December 2014, a total of 9 493 blood samples from clinically suspected dengue cases were received from different districts of the country and tested for anti-dengue IgM to confirm acute dengue virus infection.
Out of 9 493 suspected cases 3 504 (36.9%) were detected positive with IgM antibodies. Among 9 493 cases, 6 858 (72.2%) were male and 2 635 (27.8%) were female. Gender wise distribution showed that 73.6% (2 578/3 504) male and 26.4% (926/3 504) female subjects were found IgM positive. Although the male to female ratio of total reported cases was 3:1, positive rate of each tested age group showed similar rates of IgM positivity between males (37.6%) and females (35.1%) (Table 1). According to the available medical records, 5.0% (472/9,493) of dengue related deaths were reported during the last six years: 2009–2014 (Table 1).
Among 3 504 IgM positive cases, the highest positive rate (41.4%) was noticed among the individuals aged 31–40 years followed by those within 41–50 age groups (Table 2). The majority of positive cases (96.2%; 3 359/3 504) were detected during post-monsoon season (September-November) with only few cases (3.8%; 133/3 504) in other months, and the highest positive rate (45.7%) was detected in November (Table 3). Data presented in this study showed that the dengue fever cases were not evenly distributed throughout the country. The highest Mean Annual Patient Incidence during six years of study (2009–2014) was reported from Islamabad (11.03) followed by Khyber Pakhtunkhwa province, 0.45), Punjab province (0.33), Azad Jammu and Kashmir (0.28), Sindh province (0.005), and Balochistan province (0.003) (Fig. 1, Additional file 2: Table S1). The highest MAPI (11.03) rate reported for Islamabad is based on the overwhelmed number of dengue cases reported from its different hospitals that may be attributed to the availability of adequate medical and diagnostic services in the capital city compared to the other country hospitals.
Majority of the clinically suspected cases in our study were turned out as sero-negative (63.1%, 5 989/9 493) for the dengue infection and might be hospitalized due to several related febrile illnesses. In such situation, dengue incidences are mismatched between estimated and actual number of cases and need further investigations to rule out the possibility of other mosquito-borne hemorrhagic infections especially chikungunya and yellow fever . The higher incidence of infection in male subjects may reflect their higher trend of seeking medical advice and attending health units resulting in increased reporting, in contrast to females who usually prefer home remedies for cure, as evidenced in studies from India and Nepal . Being a dengue endemic country, Ae. aegypti is the most prevalent dengue vector reported in urban areas of Pakistan such as Karachi, Lahore, Rawalpindi, and Attock up to haripur district but in hilly areas such as, Abbottabad, Mansehra, Swat, and Azad Jammu and Kashmir, Ae. albopictus had also been found during the dengue season . Likewise, the dengue positive patients residing in Pakistan exhibited a wide geographic distribution, presenting four province and 99 districts.
Presence of the both DENV vector mosquitoes, Ae. aegypti and Ae. albopictus is also reported from Punjab and Khyber Pakhtunkhwa (KPK) province . The recent expansion of dengue virus infection to different parts of the country may directly be linked to climatic and human factors such as increased rainfall, floods and high population density that positively enhance the vector breeding and disease transmission efficiencies.
A few published studies on dengue in Pakistan have been reported from Karachi, Lahore and Swat [7, 8, 12, 16] indicating repeated outbreaks in Karachi during 1994–2008. Karachi is the largest and most populous metropolitan city in Pakistan and considered as one of the world’s fastest growing cities attracting migrants from all over Pakistan and South Asia. Despite these facts, our data highlights Lahore as the most affected city with higher annual dengue incidence rates compared to Karachi. This is directly reflected by the smaller number of samples from Karachi referred to NIH, Islamabad for dengue diagnostics, owing to the comparable availability of medical and diagnostics services at local hospitals and medical facilities in Karachi. Dengue virus infection was first time detected in Lahore during 2006 following by a massive outbreak during 2010–2011 with ensuing transmission to many country areas. Lahore is the second largest and most populous city in Pakistan after Karachi and its higher incidence of dengue infections may be linked with the massive to and fro population movement on daily bases. Further studies are required to investigate and rule out the true disease burden in Lahore, based on the demarcation between its indigenous population and temporary visiting patients. Furthermore, during 2010 and 2011, 40 and 362 deaths were reported respectively from Punjab province . During 2013–2014, sporadic DENV cases were reported from several country areas along with huge outbreak reported from Swat and Mansehra districts in KPK province resulting in 57 deaths in Swat and adjacent areas .
The high mortality rate during 2011–2013 in Lahore and Swat may point out multiple risk factors: a) these areas were affected by flood due to heavy rainfall which provide suitable environment for vector breeding; b) co-circulation of multiple dengue virus serotypes in these dengue endemic areas leading to significant morbidity and mortality.
In Pakistan, two standard methods, ELISA and rapid immunochromatographic test, for the diagnosis of dengue infection are available only at few major hospitals. Detection of IgM antibodies by ELISA is a sensitive marker for the identification of acute dengue virus infection. These antibodies are detectable in 50% of patients by days 3–5 after onset of illness, increasing to 80% by day 5 and 99% by day 10. In countries like Pakistan, the infected individuals’ visit the health facilities several days after the onset of disease. Considering these facts anti-dengue IgM ELISA may serve as a better diagnostic tool and be the method of choice referring to the development of IgM antibodies three to five days after the onset of clinical signs .
Presently, Pakistan lacks an active surveillance system for dengue and other arbovirus infections and solely rely on the passive surveillance system that does not cover the entire population, especially areas with poor health care settings. Development of an active surveillance system would enable health authorities to better monitor the disease incidence and transmission of DENV infection to identify high risk areas, and target dengue control activities.
There is no specific treatment available for dengue virus infection, so patient management is mainly supportive. Early diagnosis and mosquito vector control is the gold standard approach to control the dengue virus infection . Our findings emphasize that the rapid diagnostic kits to rule out the DENV infection must be available at health facilities of known endemic areas particularly during the outbreak period (post-monsoon season) for the early diagnosis and in-time management of dengue cases .
Incessant outbreaks of dengue infection in multiple geographical areas across Pakistan highlight the urgent need of a comprehensive surveillance and diagnostic system in order to identify the true disease burden and pinpoint risk factors. Further research on dengue virus infection in Pakistan should involve rapid diagnostic facilities, identifying circulating serotypes, studying vector population dynamics, implementation of sustainable vector control strategies, and public awareness on priority.
Azad Jammu & Kashmir
Annual patients’ incidence
Dengue hemorrhagic fever
Dengue shock syndrome
Enzyme linked immune-sorbent assay
World Health Organization
Johnson BW, Russell BJ, Lanciotti RS. Serotype-specific detection of dengue viruses in a fourplex real-time reverse transcriptase PCR assay. J Clin Microbiol. 2005;43(10):4977–983.
Toan DT, Hoat LN, Hu W, Wright P, Martens P. Risk factors associated with an outbreak of dengue fever/dengue hemorrhagic fever in Hanoi, Vietnam. Epidemiol Infect. 2014;143:1594–8.
WHO. Dengue, Guidelines for diagnosis, treatment, prevention and control. 2009. http://www.who.int/tdr/publications/documents/dengue-diagnosis.pdf?ua=1). Accessed 20 June 2016.
Halstead SB. Neutralization and antibody-dependent enhancement of dengue viruses. Adv Virus Res. 2003;60:421–67.
Garg A, Garg AJ, Rao YK, Upadhyay GC, Sakhuja S. Prevalence of dengue among clinically suspected febrile episodes at a Teaching Hospital in North India. J Infect Dis Immunol. 2011;3:85–9.
Bhatia R, Dash AP, Sunyoto T. Changing epidemiology of dengue in South-East Asia. WHO South-East Asia Journal of Public Health. 2013;2(1):23.
Jamil B, Hassan R, Zafar A, Bewley K, Chamberlain J, Mioulet V, Rowlands M, Hewson R. Dengue Virus Serotype 3 Karachi Pakistan. Emerg Infect Dis. 2007;13:182–3.
Khan E, Kisat M, Khan N, Nasir A, Ayub S, Hasan R. Demographic and clinical features of dengue fever in Pakistan from 2003-2007: a retrospective cross sectional study. PLoS One. 2010;5(9):e12505. doi:10.1371/journal.pone.0012505.
Rasheed SB, Butlin RK, Boots M. A review of dengue as an emerging disease in Pakistan. Public Health. 2013;127(1):11–7. doi:10.1016/j.puhe.2012.09.006.
Mahmood K, Jameel T, Aslam FH, Tahir M. Incidence of dengue haemorrhagic fever in local population of Lahore, Pakistan. Biomedica. 2009;25:93–106.
Wasay M, Channa R, Jumani M, Zafar A. Changing patterns and outcome of Dengue infection; report from a tertiary care hospital in Pakistan. J Pak Med Assoc. 2008;58(9):488–9.
Fouzia TJ, Tahir AJ, Noshin WY, Abdul M, Javed A, Umer NS, Muhammad KS. Prevalence of all four dengue serotypes confirmed by using Real Time RT-PCR among population of Lahore Pakistan. IJAVMS. 2009;3:1–3.
Fatima Z, Idrees M, Bajwa MA, Tahir Z, Ullah O, Zia MQ, et al. Serotype and genotype analysis of dengue virus by sequencing followed by phylogenetic analysis using samples from three mini outbreaks-2007–2009 in Pakistan. BMC Microbiol. 2011;11:200. doi:10.1186/1471-2180-11-200.
Koo C, Nasir A, Hapuarachchi HC, Lee KS, Hasan Z, Ng LC, et al. Evolution and heterogeneity of multiple serotypes of Dengue virus in Pakistan, 2006–2011. Virol J. 2013;10:275. doi:10.1186/1743-422X-10-275.
Rafiq MK, Afsheen A, Rasheed S. Dengue in Pakistan: Journey from a disease free to a hyper endemic nation. J Dow Univ Health Sci Karachi. 2011;5(3):81–4.
Suleman M, Faryal R, Aamir UB, Alam MM, Nisar N, Sharif S, et al. Dengue outbreak in Swat and Mansehra, Pakistan 2013; An epidemiological and diagnostic perspective. Asian Pac J Trop Med. 2016;9(4):380–4. doi:10.1016/j.apjtm.2016.03.010.
Akhtar N, Khan J, Khan A. Dengue Outbreak in Khyber Pakhtoonkhwa, Pakistan 2013. European Acad Res. 2014;1:3842–57.
Khan J, Khan I, Amin I. A comprehensive entomological, serological and molecular study of 2013 dengue outbreak of Swat, Khyber Pakhtunkhwa, Pakistan. PLoS One. 2016;11(2):e0147416. doi:10.1371/journal.pone.0147416.
Anjum BF, Azmat HK, Hazrat M. Climate Change Perspective in Pakistan. Pakistan J Meteorol. 2005;2(3):11–21.
Gupta E, Dar L, Kapoor G, Broor S. The changing epidemiology of dengue in Delhi, India. Virol J. 2006;3:92.
Pyush T, Rashmi K, Sanjeev T, Tambe JJ, Vimala V. Descriptive epidemiology of dengue virus transmission in Uttar Pradesh. Indian J Med Res. 1984;80:613–9.
WHO. Country report, Vector borne diseases in Pakistan, Directorate of Malaria Control, Government of Pakistan. Sudan: Inter country workshop Khartoum; 2003. p. 21–3.
Ahmed I, Khan D, Tariq RM, Qadri SS. Population dynamics of dengue vector Aedes aegypti L. in Thirteen Towns of Karachi, Pakistan. Int J Biotech. 2011;8:437–43.
Hunsperger EA, Yoksan S, Buchy P, Nguyen VC, Sekaran SD, et al. Evaluation of Commercially available anti-dengue virus immunoglobulin M Tests. Emerg Infect Dis. 2009;15:436–40.
Sankar SG, Dhananjeyan KJ, Paramasivean R, Thenmozhi V, Tyagi BK, Vennison SJ. Evaluation and use of NS1 IgM antibody detection for acute dengue virus diagnosis: report from an outbreak investigation. Clin Microbiol Infect. 2012;18:E8–E10.
Amin AAA, Hussain AMZ, Murshed M, Chowdhury IA, et al. Serodiagnosis of dengue infection by haemagglutination inhibition test (HI) in suspected cases in Chittagong, Bangladesh. Dengue Bull. 1999;23:34–8.
We would like to acknowledge the support we received from the administration and medical staff working at various hospitals in KPK Province. We especially thankful to Dr. Bilal Bahrawar Khan, Senior Epidemiologist, Khyber Pakhtunkhwa; Mian Sufian Mr. Umer Daraz, and Mr. Yasir Arshad from Department of Virology, National Institute of health for their technical support in sample collection and transportation.
The authors funded the study themselves.
Availability of data and materials
"The datasets supporting the conclusions of this article are included within the article and its additional files."
SSZZ, MMA, UZBA, HWL and MS conceived and designed the study. HWL, MMA, SS, SS; MSR analyzed data and wrote the manuscript. MSR and AK performed the laboratory tests. MA, MU and MRS collected patients’ information and performed analysis. “All authors read and approved the final version of the manuscript″.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study was approved by the Internal Review board of National Institute of Health, Islamabad, Pakistan
Consent to participants
A written informed consent was obtained from the patients/parents or guardians before the collection of blood samples.
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Suleman, M., Lee, HW., Zaidi, S.S.Z. et al. Preliminary Seroepidemiological survey of dengue infections in Pakistan, 2009-2014. Infect Dis Poverty 6, 48 (2017). https://doi.org/10.1186/s40249-017-0258-6