

Page 29
Notes:
conferenceseries
.com
Volume 6, Issue 2 (Suppl)
Virol-mycol
ISSN: 2161-0517 VMID, an open access journal
Virology Asia 2017
May 11-12, 2017
May 11-12, 2017 Singapore
10
th
World Congress on
Virology and Mycology
Prevalence of dengue virus and their serotypes causing infection in eastern UP, India
Amresh Kumar Singh, Ruchi Mishra, Jayesh Pandey and Kusum Jasuja
BRD Medical College Gorakhpur, India
Statement of the Problem:
Dengue is one of themost seriousmosquito borne viral infections and in India it has dramatically expanded
over the last few decades, with rapidly changing epidemiology. The spectrum of manifestations is ranging from asymptomatic/mild
to dengue hemorrhagic fever (DHF), to a shock syndrome (DSS). Recent research shows that there is a clear shift in dengue virus
(DENV) having mortality 0.5–3.5% in DENV-2. So, this study was conducted to know the prevalence of dengue by different methods,
serotypes and its impact in epidemiology, mortality in UP, India.
Methodology & Theoretical Orientation:
Prospectively designed study was performed and all laboratory records were analyzed.
Blood samples were tested for dengue NS1 antigen, IgM antibodies, and nucleic acid detection by; dengue early NS1 enzyme linked
immune sorbent assay (ELISA), IgM capture ELISA, and real time reverse transcriptase PCR (RT-PCR), respectively. Descriptive
statistics were used and data were expressed in proportions. Nested RT-PCR was performed for serotyping.
Findings:
Out of total 863 samples tested, 203 (23.52%) were found positive for dengue virus infection by combination of different
methods with male preponderance (65%). Seasonal trend showed a gradual increase; starting from July with a peak in September
(34.5%). The most common presentation was fever (97%), only 1% cases presented with hemorrhagic manifestations. Out of total of
203 cases, 176 (86.7%) patients had fever, 16 (7.9%) DHF and 11 (5.4%) had DSS. Dengue IgG prevalence increased with age, with the
lowest (16.3%) in <20 years and the highest (78.3%) in 20-40 years. The range of platelet count was; 1,69,000-11000/cumm. A total
of 189/863 (21.9%) specimens were positive for NS1, 64/863 (7.4%) for IgM and 177/863 (20.5%) positive by nested RT-PCR. Of 203
positive cases, maximum serotypes were 123 (60.6%) for DENV-2 and mixed serotypes in 06 (2.96%) patients. Mortality was seen in
15 cases (7.4%), with maximum occurring in 2016.
Conclusion&Significance:
Dengue has established its transmission and high prevalence (23.52%) inUPwith predominantly affecting
adult males and preponderance by DENV-2 virus (60.6%). This study thus emphasizes the need for continuous sero-epidemiological
diagnosis/surveillance for effective dengue control in India.
Biography
Amresh Kumar Singh has expertise in different disciplines of Clinical Microbiology and Infectious Diseases Evaluation and passion in improving the health and
wellbeing of people living in Eastern UP, India. He has published many national as well as international journals and has teaching experience in teaching MBBS
students, BSc (Nursing), MSc (Microbiology) and MD. He participated in project for detection of antimicrobial resistance in Gram negative
bacilli
, and Gram positive
cocci
like, ESBLs, AmpC, MBLs, MRSA, VRE etc. He worked on diagnostic mycobacteriology (culture and antimicrobial sensitivity techniques including culture on
standard media, BacT/ALERT® 3D system, Mycobacteria growth indicator tube (MGIT) and
Mycobacterium tuberculosis
direct detection methods), antimicrobial
susceptibility testing in
M. tuberculosis
complex (MTBC) and NTM (conventional and DNA-based methods) like line probe assay and mutational study; Virology-
especially in dengue virus, HIV, enteroviruses (AES), viral encephalitis, acute hemorrhagic viral infection for their diagnosis and; tissue culture techniques for
isolation and identification of different medically important viruses for PCR (conventional, nested, Real-time RT-PCR), DNA sequencing, spoligotyping, pulse-field
gel electrophoresis, etc.
amresh.sgpgi@gmail.comAmresh Kumar Singh et al., Virol-mycol 2017, 6:2 (Suppl)
http://dx.doi.org/10.4172/2161-0517-C1-020