Short Communication - (2022) Volume 19, Issue 7
Dengue and Dengue Haemorrhagic Fever Outbreak in Thailand: A Tropical Infectious Disease Leads to a Critical Potential Healthcare Threat in
a Developing Country
Naluepanat Yodjan*
1Department of Medical Science, Naresuan University, Thailand
*Correspondence:
Naluepanat Yodjan,
Department of Medical Science, Naresuan University,
Thailand,
Email:
Received: 29-Jun-2022, Manuscript No. IPDEHC-22-14254;
Editor assigned: 01-Jul-2022, Pre QC No. IPDEHC-22-14254 (PQ);
Reviewed: 15-Jul-2022, QC No. IPDEHC-22-14254;
Revised: 20-Jul-2022, Manuscript No. IPDEHC-22-14254 (R);
Published:
27-Jul-2022, DOI: 10.21767/2049-5471.19.7.34
Abstract
Dengue virus (DENV), a positive-sense single-stranded RNA virus belonging to the family of Flaviviridae, is transmitted to humans mainly by female mosquito bites. Its clinical features range from asymptomatic presentation to severe haemorrhagic fever. DENV has bedevilled several developing countries worldwide, including Thailand. An increasing outbreak in Thailand by DENV indicates circulating among mosquitoes and humans again. Concerned authorities should act to support and development healthcare systems, including research funding, leading to infection control and prevention efficiency
Keywords
Dengue fever; Dengue haemorrhagic fever; Virus; Healthcare; Infection
Introduction
Mosquitoes are important reservoir hosts for multiple pathogenic
viruses, similarly to bats and rodents [1,2]. They have
been associated with the Chikungunya virus, Zika virus, West
Nile virus, and Dengue virus [3-6]. First isolated from blood
specimens in 1943 in Japan, the Dengue virus (DENV) is a mosquito-
borne pathogen, a positive-sense single-stranded RNA
virus of the family Flaviviridae [7,8]. DENV is a significant tropical
infectious disease and has become a public health issue.
DENV is transmitted to humans through the bites of infected
female mosquitoes, primarily the Aedes aegypti mosquito and
forest mosquito Aedes albopictus [9]. However, there is evidence
of infections through organ transplants and blood transfusions
[10,11].
Description
DENV have a vast spectrum of clinical manifestations, ranging
from asymptomatic to flu-like, known as Dengue Fever (DF)
and severe form of Dengue disease (SDD), including Dengue
Haemorrhagic Fever (DHF) and Dengue Shock Syndrome (DSS) [12-14]. The general clinical manifestations represented severe
headache, pain behind the eyes, muscle and joint pains, nausea,
vomiting, diarrhoea, swollen glands, and rash. The severe
form of Dengue can lead to threatening complications, including
plasma leaking, fluid accumulation, respiratory dysfunction,
severe haemorrhage, or organ failure, and it is a potentially
fatal complication [15-18]. Diagnosis of viral infections is dependent
on immune-chromatographic tests, Hemagglutination
Inhibition Assay (HIA), Enzyme-Linked Immunosorbent Assay
(ELISA), and Reverse Transcriptase Polymerase Chain Reaction
(RT-PCR) can deliver the diagnostic results of clinical specimens
[19-22]. Currently, there are no specific-antiviral drugs or vaccine
for the virus and therapy is mainly supportive treatment.
The DENV has been outbreak worldwide, including in the USA,
Gabon, India, Malaysia, China, Italy, and Thailand [23-28]. Thailand
has been under its pounce in Southeast Asia; a review
reported by Yodjan indicated that from 2007 to 2021, the Dengue
virus was responsible for more than 1,000,000 confirmed
cases and approximately 1,067 deaths in the country, and the
incidence rate of Dengue and Dengue Haemorrhagic Fever varies between 62.33 to 241.03 per 100,000 inhabitants. In 2021,
9,235 cases were confirmed, and it is noted that the number
of patients significantly decreased compared to the preceding
year [9]. However, currently 9 September 2022, reports of the
DENV outbreak are circulating among mosquitoes and humans
again. The number of patients is significantly increasing; more
than 19,000 cases have been confirmed, with 14 deaths [29].
These situations reflect that disease surveillance systems and
control of vector-borne disease ecology are not efficient. All
precautionary actions must be employed to guarantee that
the country does not undergo another healthcare threat. Government
must allot more funds to the healthcare systems and
research. In addition, a highly proficient development assay
should be familiarized to distinguish between different flavivirus.
As the significant transmission origin of DENV remains in
mosquitoes, a particular focus must be applied to introducing
high sanitation facilities across the country and ensuring the
control of the mosquito populations is efficient due to Thailand
is at medically significant risk of contracting multiple arboviruses,
such as Dengue, Chikungunya and Zika virus.
Conclusion
Public awareness campaigns engage and educate local communities,
enlightening the masses on personal hygiene and mosquito
repellants. A public health database for correctly reporting
any infection case must be well-developed. Moreover, research
programs should be developed to control vector-borne transmissions,
disease ecology, and drug development. As a country
still recovering from the COVID-19 pandemic, a potential
threat of DENV can lead to a disastrous knock, further depriving
Thailand of healthcare systems. Therefore, the concerned
authorities must take immediate action, or DENV can be the
next public health threat to the country.
Author Contributions
Naluepanat Yodjan
Conceptualization, data curation, formal analysis, investigation,
methodology, validation, visualization, writing-original
draft, and writing-review and editing.
Conflicts of Interest
The author declares that there is no conflict of interests.
Funding Information
The author has not received any financial support for this manuscript.
Ethical Approval
Not Applicable.
Consent for Publication
Not Applicable.
Acknowledgements
None.
REFERENCES
- O’shea TJ, Cryan PM, Cunningham AA, Fooks AR, Hayman DT, et al. (2014) Bat flight and zoonotic viruses. Emerg Infect Dis 20: 741.
[Crossref] [Google Scholar]
- Yodjan N (2022) Virome diversity in rodents and their zoonotic viral infectious diseases: An essential reservoir of emerging and re-emerging viruses infecting humans. Access Microbiology.
[Crossref] [Google Scholar]
- Presti AL, Lai A, Cella E, Zehender G, Ciccozzi M (2014) Chikungunya virus, epidemiology, clinics and phylogenesis: A review. Asian Pac J Trop Med 7: 925-932.
[Crossref] [Google Scholar]
- Benelli G, Romano D (2017) Mosquito vectors of Zika virus. Entomol Gen 36: 309-318.
[Crossref] [Google Scholar]
- Turell MJ, Dohm DJ, Sardelis MR, O’guinn ML, Andreadis TG, et al. (2005) An update on the potential of North American mosquitoes (Diptera: Culicidae) to transmit West Nile virus. J Med Entomol 42: 57-62.
[Crossref] [Google Scholar]
- Halstead SB (2008) Dengue virus-mosquito interactions. Annu Rev Entomol 53: 273-291.
[Crossref] [Google Scholar]
- Messina JP, Brady OJ, Scott TW, Zou C, Pigott DM, et al. (2014) Global spread of dengue virus types: Mapping the 70 year history. Trends Microbiol 22: 138-146.
[Crossref] [Google Scholar]
- Harris E, Holden KL, Edgil D, Polacek C, Clyde K (2006) Molecular biology of flaviviruses. Novartis foundation symposium. Wiley Online Library 23.
[Crossref] [Google Scholar]
- Yodjan N (2022) A review of dengue and dengue haemorrhagic fever amidst the COVID-19 pandemic in Thailand: A raising concern and public health nested crises. Access Microbiol.
[Crossref] [Google Scholar]
- Rosso F, Pineda JC, Sanz AM, Cedano JA, Caicedo LA (2018) Transmission of dengue virus from deceased donors to solid organ transplant recipients: Case report and literature review. Braz J Infect Dis 22: 63-69.
[Google Scholar]
- Tambyah PA, Koay ES, Poon ML, Lin RV, Ong BK (2008) Dengue hemorrhagic fever transmitted by blood transfusion. N Engl J Med 359: 1526-1527.
[Crossref] [Google Scholar]
- Seneviratne S, Gurugama P, Garg P, Perera J, Wijewickrama A (2010) Dengue viral infections. Indian J Dermatol 55.
[Crossref] [Google Scholar]
- Chevillon C, Failloux AB (2003) Questions on viral population biology to complete dengue puzzle. Trends Microbiol 11: 415-421.
[Crossref] [Google Scholar]
- Noisakran S, Perng GC (2008) Alternate hypothesis on the pathogenesis of dengue hemorrhagic fever (DHF)/Dengue Shock Syndrome (DSS) in Dengue virus infection. Exp Biol Med 233: 401-408.
[Crossref] [Google Scholar]
- Bhattacharya K, Chaudhuri AK, Das A, Banerjee DK (2022) A Data Mining based study on Dengue Fever: A Review. International Research Journal on Advanced Science Hub 4: 101-107.
[Crossref] [Google Scholar]
- Daniel J, Irin Sherly S, Ponnuramu V, Pratap singh D, Netra S, et al. (2022) Recurrent neural networks for feature extraction from Dengue fever. Evid Based Complement Alternat Med 2022: 9.
[Crossref] [Google Scholar]
- Babu DS, Raju B, Swapna S, Kolluri J, Ramesh D, et al. (2022) Dengue symptoms classification analysis with improved conditional probability decision analysis. Appl Nanosci 1-9.
[Crossref] [Google Scholar]
- Chan M, Johansson MA (2012) The incubation periods of Dengue viruses. PloSOne 7: e50972.
[Crossref] [Google Scholar]
- Vaughn DW, Nisalak A, Kalayanarooj S, Solomon T, Dung NM, et al. (1998) Evaluation of a rapid immunochromatographic test for diagnosis of Dengue virus infection. J Clin Microbio 36: 234-238.
[Crossref] [Google Scholar]
- Sirikajornpan K, Nisalak A, Thaisomboonsuk B, Buddhari D, Yoon IK, et al. (2018) Comparison of anti-DENV/JEV IgG-mAb enzyme-linked immunosorbent assay and hemagglutination inhibition assay. Proquest 49(4): 629-638.
[Google Scholar]
- Wang SM, Sekaran SD (2010) Evaluation of a commercial SD dengue virus NS1 antigen capture enzyme-linked immunosorbent assay kit for early diagnosis of dengue virus infection. J Clinic microbiol 48: 2793-2797.
[Crossref] [Google Scholar]
- Rosen L, Drouet MT, Deubel V (1999) Detection of Dengue virus RNA by reverse transcription-polymerase chain reaction in the liver and lymphoid organs but not in the brain in fatal human infection. Am J Trop Med Hyg 61: 720-724.
[Crossref] [Google Scholar]
- Teets FD, Ramgopal MN, Sweeney KD, Graham AS, Michael SF, et al. (2014) Origin of the Dengue virus outbreak in Martin County, Florida, USA 2013. Virol Rep 1: 2-8.
[Crossref] [Google Scholar ]
- Leroy EM, Nkoghe D, Ollomo B, Nze-Nkogue C, Becquart P, et al. (2009) Concurrent chikungunya and Dengue virus infections during simultaneous outbreaks, Gabon, 2007. Emerg Infect Dis 15: 591.
[Crossref] [Google Scholar]
- Bharaj P, Chahar HS, Pandey A, Diddi K, Dar L, et al. (2008) Concurrent infections by all four Dengue virus serotypes during an outbreak of dengue in 2006 in Delhi, India. Virol J 5: 1-5.
[Crossref] [Google Scholar]
- Lee H, Rohani A (2005) Transovarial transmission of Dengue virus in Aedes aegypti and Aedes albopictus in relation to Dengue outbreak in an urban area in Malaysia.
[Google Scholar]
- Xu G, Dong H, Shi N, Liu S, Zhou A, et al. (2007) An outbreak of Dengue virus serotype 1 infection in Cixi, Ningbo, People’s Republic of China, 2004, associated with a traveler from Thailand and high density of Aedes albopictus. Am J Trop Med Hyg 76: 1182-1188.
[Google Scholar]
- Lazzarini L, Barzon L, Foglia F, Manfrin V, Pacenti M, et al. (2020) First autochthonous Dengue outbreak in Italy, August 2020. Euro Surveill 25: 2001606.
[Crossref] [Google Scholar]
- Office of disease prevention and control 3, N. S. 2022.
Citation: Syed AJ (2022) The Increase in Security Breaches Through Remote Working. Divers Equal Health Care. 19:35.
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