Abstract

Dengue fever is the most prevalent arboviral disease in the tropical and sub-tropical regions of the world. The present report describes molecular detection and serotyping of dengue viruses in acute phase blood samples collected from New Delhi, India. Phylogenetic and molecular clock analysis of dengue virus serotype 1 and 3 strains were also investigated. Dengue virus infection was detected in 68.87% out of 604 samples tested by RT-PCR between 2011 & 2014. Dengue serotype 1 was detected in 25.48% samples, dengue serotype 2 in 79.56% samples and dengue serotype 3 in 11.29% samples. Dengue serotype 4 was not detected. Co-infection by more than one dengue serotype was detected in 18.26% samples. Envelope gene of 29 DENV-1 and 14 DENV-3 strains were sequenced in the study. All the DENV-1 strains grouped with the American African genotype. All DENV-3 strains were found to belong to Genotype III. Nucleotide substitution rates of dengue 1 and 3 viruses were determined in the study. Time to the most recent common ancestor (TMRCA) of dengue 1 viruses was determined to be 132 years. TMRCA of DENV-3 viruses was estimated to be 149 years. Bayesian skyline plots were constructed for Indian DENV-1 and 3 strains which showed a decrease in population size since 2005 in case of DENV- 1 strains while no change was observed in recent years in case of DENV-3 strains. The study also revealed a change in the dominating serotype in Delhi, India in recent years. The study will be helpful in formulating control strategies for the outbreaks. In addition, it will also assist in tracking the movement and evolution of this emerging virus.

Highlights

  • Dengue is a mosquito-borne acute viral infection prevalent in tropical and subtropical areas of the world

  • The present study reports the prevalence of dengue viruses in the city of New Delhi, India

  • Dengue serotype 2 was detected in 80% of the dengue positive samples while dengue serotype 4 was not detected at all

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Summary

Introduction

Dengue is a mosquito-borne acute viral infection prevalent in tropical and subtropical areas of the world. During the first 4–5 days of the disease onset, virus culture, RT-PCR and NS1 antigen ELISA are the methods of choice for diagnosis of dengue as the virus is detectable in plasma, serum, circulating blood cells and other tissues. After this duration serological methods are preferred as the host antibodies could be detected by this time [1]. The present study reports genetic characterization of DENV-1 and 3 strains circulating in 2012–2014 in Delhi, India. Past population dynamics of Indian DENV-1 and 3 strains based on Bayesian skyline plots were investigated

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