|SHORT RESEARCH COMMUNICATION
|Year : 2017 | Volume
| Issue : 4 | Page : 369-371
Scrub typhus in Mizoram, India
H Lalrinkima1, R Lalremruata2, C Lalchhandama3, Lalthansanga Khiangte4, Freddy H Siamthara1, C Lalnunpuia1, SK Borthakur1, Gautam Patra1
1 Department of Parasitology, College of Veterinary Sciences and Animal Husbandry, Central Agricultural University, Aizawl, India
2 Department of Microbiology, Synod Hospital, Aizawl, India
3 Department of Toxicology, College of Veterinary Sciences and Animal Husbandry, Central Agricultural University, Aizawl, India
4 Department of Animal Genetics and Breeding, College of Veterinary Sciences and Animal Husbandry, Central Agricultural University, Aizawl, India
|Date of Submission||26-Jul-2017|
|Date of Acceptance||15-Nov-2017|
|Date of Web Publication||19-Feb-2018|
Department of Parasitology, College of Veterinary Sciences & Animal Husbandry, Central Agricultural University, Aizawl, Mizoram–796 014
Source of Support: None, Conflict of Interest: None
Keywords: IgM rapid ICT-test kit; India; Mizoram; Scrub typhus; seroprevalence
|How to cite this article:|
Lalrinkima H, Lalremruata R, Lalchhandama C, Khiangte L, Siamthara FH, Lalnunpuia C, Borthakur S K, Patra G. Scrub typhus in Mizoram, India. J Vector Borne Dis 2017;54:369-71
|How to cite this URL:|
Lalrinkima H, Lalremruata R, Lalchhandama C, Khiangte L, Siamthara FH, Lalnunpuia C, Borthakur S K, Patra G. Scrub typhus in Mizoram, India. J Vector Borne Dis [serial online] 2017 [cited 2021 Apr 19];54:369-71. Available from: https://www.jvbd.org/text.asp?2017/54/4/369/225844
Scrub typhus is caused by Orientia tsutsugamushi, (‘tsutsuga’ means something small and dangerous and ‘mushi’ means insect/mite/creature) which circulates mainly between human and rodents. Clinical signs and symptoms include febrile condition, headache, eschar, lymphadenopathy, muscular pain and gastrointestinal disorders which in severe and untreated case may end into fatal multiple organ failure,,,,,,. The observation of the eschar is often missed and other symptoms ofthe disease are not characteristic thus posing the problem of delayed diagnosis by the clinician. Although, scrub typhus is known since 1889 in Japan, the severe epidemics of scrub typhus in Burma (Myanmar) and Ceylon (Sri Lanka) during World War II intensified the interest of studying about this disease. Scrub typhus is endemic in a region called ‘tsutsugamushi triangle’ which extends from northern Japan and far-eastern Russia in the north, to the territories around the Solomon Sea into northern Australia in the south and to Pakistan and Afghanistan in the west,. In India, scrub typhus was first reported from Assam and West Bengal states during World War II. The disease is being reported in many endemic pockets of different states of India such as Maharashtra, Tamil Nadu, Karnataka, Kerala, Jammu and Kashmir, Uttarakhand, Himachal Pradesh, Rajasthan, West Bengal, Assam, Arunachal Pradesh, Sikkim, Nagaland and Meghalaya,,,,,.
Vaccination against this scourge faces challenging obstacles such as extensive antigenic diversity and short duration of immune protection following immunity stimulated by naturally acquired scrub typhus infection. Moreover, immunity to the homologous strain wanes over a period of few years. In the present situation, early diagnosis and chemotherapy is the only choice for combating scrub typhus infection and reducing associated mortality. Diagnosis of scrub typhus is carried out mainly by serological assays, though in recent years, there are specific molecular detection techniques employing amplification of different target genes by polymerase chain reaction.
The immunofluorescence assay (IFA) is considered as ‘gold standard’ for diagnosing rickettsial infections but faces certain demerits like its cost-effectiveness in developing countries and technical expertness. One of the most widely used serological assay, Weil-Felix test suffers from poor sensitivity and specificity. Scrub typhus ELISA, which uses O. tsutsugamushi recombinant p56 kD type-specific antigen of Karp, Kato, Gilliam and TA716 strains has > 90% sensitivity and specificity for detecting specific antibodies,. However, the samples are usually examined multiple times for ELISA test thereby causing delay in diagnosis. On the contrary, rapid detection in immunochromatographic test format can identify a single sample in short span of time.
The present study was carried out to know the current status of the prevalence of scrub typhus in Mizoram from clinically suspected patients who were admitted to Synod Hospital, Aizawl, Mizoram by rapid-ICT test kit. A cross-sectional study was conducted from October 2014 to December 2016 on serum samples of patients with undifferentiated fever from different parts of Mizoram admitted to the Synod Hospital, Mizoram. The samples were examined for detection of anti-OrientiaIgM antibody in rapid-ICT test having sensitivity of 98.6% and specificity of 98.2% (ImmuneMed scrub typhus rapid test kit, South Korea). Clinical samples were collected after taking informed consent from the patients.
A total of 4081 sera samples were examined for the presence of anti-Orientia IgM antibody in the human subjects. The result revealed that 6.9% (n=283) samples were positive in the test kit, irrespective of age and gender. The percentage of seropositivity was higher during the winter (November–February) at 13.5% (154/1141) followed by autumn (September–October) at 10.9% (141/1287). In summer and spring seasons the percentages were comparatively lower at levels of 4.8 and 5.5%, respectively. Age wise comparison of the prevalence indicated that 21–30 yr age group were most affected (prevalence 23.7%) followed by 31–40 yr age group (20.8%). The age groups of 1–10 and 41–50 yr showed least seropositivity (9.2% each). The seropositivity for the age groups, 11–20, 51–60 and ≥60 yr was in between these two extremes, i.e. 13.4, 11.7 and 12.0%, respectively [Figure 1]. The gender-wise comparison showed that males (56.2%) were having higher prevalence rate than females (43.8%), irrespective of age and season [Table 1].
|Figure 1: Pie-chart representing age-wise comparison of seropositivity of scrub typhus in Mizoram (October 2014 to December 2016). Higher prevalence was observed in 21–30 and 31–40 yr age groups.|
Click here to view
The overall prevalence of 6.9% in the present study was found to be lower in comparison to the earlier reports from different parts of India. The seropositivity of the results reported from the neighbouring states of northeastern India, i.e. Nagaland, Meghalaya and Arunachal Pradesh by indirect ELISA were 36.55, 53.33 and 40%, respectively,. The comparatively higher incidence of scrub typhus during autumn (11%) and winter (13.5%) in the present study may be due to increased human activities in the agricultural fields and bushes during these seasons, as there is relatively moderate climate in sub-tropical forests and accumulation of post-harvest paddy straw attracts rodent population, both contributing as deciding factors for scrub typhus transmission. Similar pattern of the disease occurrence has been reported from southern states of India where higher incidence was recorded in colder season of the year,; on the contrary, northern India and other southeast Asian countries encountered the disease at highest rate during rainy season of the year,,. The demographic characteristic in the seropositivity of scrub typhus varied with age and gender. The study results showed higher seropositivity in two age groups, viz. 21–30 and 31–40 yr; affecting predominantly males corroborating with earlier reports,,. The higher outdoor and agricultural activities by males could be the reason of higher seropositivity of scrub typhus in this gender.
In India, the first case of scrub typhus was reported from Assam and West Bengal in the year 1945; and the re-emergence of this scourge was reported in 2010 after a gap of 65 yr. Since then, there are little documentations about the incidences and seropositivity of scrub typhus from northeast India,. The subtropical rain forest of Northeast India is conducive for vector propagation and at the same time is vulnerable to climate change. There has been considerable debate as to whether global risk from vector-borne diseases will be impacted by climate change; however, this debate has mostly ignored the biological diversity of vectors and vector-borne diseases. Therefore, detailed studies on the correlation between the recent resurgence of scrub typhus in northeastern India and the climate change is warranted.
In conclusion, this study briefly describes the seroprevalence of scrub typhus in Mizoram state of northeastern India, where during post-monsoon autumn and winter seasons the increased human activities in bushes and agricultural fields have impacted upon the higher rate of scrub typhus incidences. Preventive measures like protective clothings and application of insect repellents along with public awareness about the disease transmission dynamics are important for reducing the disease prevalence.
Conflict of interest: None to declare.
The study does not involve ethical issues.
| Acknowledgements|| |
The authors sincerely acknowledge the Director, Synod Hospital, Aizawl for providing necessary data and the Dean, College of Veterinary Sciences and Animal Husbandry, Selesih, Aizawl for providing necessary facilities.
| References|| |
Kumar D, Raina DJ, Gupta S, Angurana A. Epidemiology of scrub typhus. JK Sci
Ramyasree A, Kalawat U, Rani ND, Chaudhury A. Seroprevalence of scrub typhus at a tertiary care hospital in Andhra Pradesh. Indian J Med Microbiol
2015; 55(1): 68-72.
Khan F, Mittal G, Agarwal RK, Ahmad S, Gupta S, Shadab M. Prevalence of scrub typhus–A cause of concern in Uttarakhand region, India. Int J Curr Microbiol App Sci
Kalal BS, Puranik P, Nagaraj S, Rego S, Shet A. Scrub typhus and spotted fever among hospitalised children in south India: Clinical profile and serological epidemiology. Indian J Med Microbiol
Varghese GM, Raj D, Francis MR, Sarkar R, Trowbridge P, Muliyi J. Epidemiology and risk factors of scrub typhus in south India. Indian J Med Res
2016; 144(1): 76-81.
Khan SA, Khamo V, Uriah HJ, Bora T, Dutta P. Scrub typhus in hilly regions of northeast India. Indian J Med Res
2016; 144(1): 138-40.
Walker DH. Scrub typhus-scientific neglect, ever-widening impact. New England J Med
Audy JR. Red mites and typhus
. London: University of London, Athlone Press 1968; p. 191.
Davis GE, Austrian RC, Bell EJ. Observations on tsutsugamushi disease (scrub typhus) in Assam and Burma: The recovery of strains of Rickettsia orientalis. Am J Trop Med Hyg
Kingston HWF, Blacksell SD, Tanganuchitcharnchai A, Laongnualpanich A, Basnyat B, Day NP, et al
. Comparative accuracy of the InBios scrub typhus detect IgM rapid test for the detection of IgM antibodies by using conventional serology. Clin Vaccine Immunol
2015; 22(10): 1130-2.
Velmurugan A, Selvaraj S, Pradeep J, Park S, Kim SH, Kim YJ, et al
. Serological diagnosis of acute scrub typhus in southern India: Evaluation of InBios scrub typhus detect IgM rapid test and comparison with other serological tests. J Clin Diag Res
Kim YJ, Park S, Premaratna R, Selvaraj S, Park SJ, Kim S, et al
. Clinical evaluation of rapid diagnostic test kit for scrub typhus with improved performance. J Korean Med Sci
2016; 31(18): 1190-6.
Jakharia A, Borkakoty B, Biswas D, Yadav K, Mahanta J. Seroprevalence of scrub typhus infection in Arunachal Pradesh, India. Vector Borne Zoonotic Dis
2016; 16(10): 659-63.
Mahajan SK, Rolain JM, Kashyap R, Bakshi D, Sharma V, Prasher BS,et al
. Scrub typhus in Himalayas. Emerg Infect Dis
2006; 12(10): 1590-2.
Sun Y, Wei YH, Yang Y, Ma Y, de Vlas SJ, Yao HW, et al
. Rapid increase of scrub typhus incidence in Guangzhou, southern China, 2006-2014. BMC Infect Dis
2017; 17(1): 13.
Lee YS, Wang PH, Tseng SJ, Ko CF, Teng HJ. Epidemiology of scrub typhus in eastern Taiwan, 2000-2004. Jpn J Infect Dis
Khan SA, Dutta P, Khan AM, Topno R, Borah J, Chowdhury P, et al
. Re-emergence of scrub typhus in Northeast India. Int J Infect Dis
2012; 16(12): e889-e890.
Ravindranath NH, Rao S, Sharma N, Nair M, Gopalakrishnan R, Rao AS, et al
. Climate change vulnerability profiles for Northeast India. Curr Sci
2011; 101(41): 384-94.
Ogden NH, Robbin Lindsay L. Effects of climate and climate change on vectors and vector-borne diseases: Ticks are different. Trends Parasitol
2016; 32(8): 646-56.
|This article has been cited by|
||Seropositivity of Scrub Typhus Inpatients Attending a Tertiary Care Hospital in Western Odisha
| ||Shuvankar Mukherjee,Anshuman Dash,Shreekant Tiwari |
| ||Journal of Evolution of Medical and Dental Sciences. 2020; 9(04): 178 |
|[Pubmed] | [DOI]|
||Rickettsial disease existence in India: resurgence in outbreaks with the advent of 20th century
| ||Abha Sharma,Bibhabati Mishra |
| ||Indian Journal of Health Sciences and Biomedical Research (KLEU). 2020; 13(1): 5 |
|[Pubmed] | [DOI]|
||Scrub typhus in patients with acute febrile illness: a 5-year study from India
| ||C K Thakur,R Chaudhry,N Gupta,E V Vinayaraj,V Singh,B K Das,R S Jadon,N Wig,R Lodha,S K Kabra,A B Dey,M Chhabra |
| ||QJM: An International Journal of Medicine. 2019; |
|[Pubmed] | [DOI]|