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Volume 27, Number 7—July 2021
Dispatch

Retrospective Study of Kyasanur Forest Disease and Deaths among Nonhuman Primates, India, 1957–2020

Sulagna Chakraborty, William E. SanderComments to Author , Brian F. Allan, and Flavia C.D. Andrade
Author affiliation: University of Illinois Urbana–Champaign, Urbana–Champaign, Illinois, USA

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Abstract

Kyasanur Forest disease (KFD) is a tickborne hemorrhagic disease affecting primates along the Western Ghats mountain range in India. Our retrospective study indicated that >3,314 monkey deaths attributed to KFD were reported in KFD-endemic states in India during 1957–2020. These data can help guide surveillance to protect animal and human health.

Figure 1

Ecology of Kyasanur Forest disease virus. Reproduced from https://www.cdc.gov/vhf/kyasanur/resources/virus-ecology.html.

Figure 1. Ecology of Kyasanur Forest disease virus. Reproduced from https://www.cdc.gov/vhf/kyasanur/resources/virus-ecology.html.

Kyasanur Forest disease (KFD) is a highly infectious tickborne disease affecting humans and monkeys. The etiologic agent of this disease is the Kyasanur Forest disease virus (KFDV), a flavivirus. Since its discovery in 1957 in Karnataka State, India, KFD has expanded to 5 states along the western coastline in India (1) and ≈10,000 reported cases of KFD in humans, averaging 400–500 cases annually (2). After an incubation period of 3–8 days, primary clinical symptoms include fever, myalgia, and gastrointestinal and bleeding problems. In a small subset of patients, a second phase of the disease can include neurologic manifestations and fever. If the disease is detected early, symptomatic supportive care can improve recovery from the disease. Case-fatality rates range from 3% to 15% (1,3). The primary vectors of KFDV are Haemaphysalis spinigera and H. turturis ticks, which are endemic to southern India and transmit the virus to monkeys and humans (4). Larvae and nymphs of these ticks feed on monkeys when the monkeys are ground foraging, providing routes of infection and spread. In addition, KFDV can be transmitted transovarially in these ticks (Figure 1).

Macaca radiata and Semnopithecus entellus are 2 monkey species in the KFD-endemic region frequently associated with KFD; these monkeys can succumb to the virus quickly (3). For monkeys, KFDV causes nonspecific and degenerative changes in abdominal organs, hemorrhage, and encephalitis. Experimentally infected monkeys have diarrhea, bradycardia, and hypotension and ultimately die (5). Monkey migration might expand KFDV geographic distribution, in which infected ticks are carried across state borders through connected natural areas (1,3,4). Although reporting of monkey deaths from KFD during the past 60 years has been unsystematic and inconsistent, the data provide valuable information. We summarize reports of monkey deaths connected with KFD in India and evaluate the utility of reporting KFD occurrence in monkeys for human disease surveillance.

The Study

We conducted a retrospective review of scientific literature through Web of Science, PubMed Central, and Google Scholar and included data from Pro-MED Mail, newspapers, and government reports issued during 1957–2020. The search keywords included KFD, KFDV, monkey fever, Kyasanur Forest disease, and mankan kayla (a local term in Karnataka, India). We used 55 peer-reviewed journal articles, 109 Pro-MED Mail reports, 1 report by the Karnataka State government, and 1 newspaper report to generate estimates. We created a database from all information sources; our final dataset (Table 1) contains the most updated information for all years from the available data.

Information on monkey deaths caused by KFD is limited, particularly for species-specific deaths. Our review of all data sources indicates that >3,314 monkey deaths associated with KFD were reported during 1957–2020 (Table 1). However, only a subset of deaths were tested for KFDV. During this period, 760 monkeys underwent necropsy, and 334 were laboratory-confirmed to have KFDV infection (Appendix). Of the reported monkey deaths, a total of 1,676 deaths occurred in S. entellus monkeys and 400 deaths occurred in M. radiata monkeys; species were not reported for the remaining 1,238 deaths.

Figure 2

Hotspot areas for human cases and monkey deaths attributable to Kyasanur Forest disease, India,1957–2020. Inset map shows the region in context of the Indian subcontinent.

Figure 2. Hotspot areas for human cases and monkey deaths attributable to Kyasanur Forest disease, India,1957–2020. Inset map shows the region in context of the Indian subcontinent.

We found an early report of KFD in monkeys outside of Karnataka in Tamil Nadu state in 2012, which could be linked to an outbreak of human cases at the Bandipur Tiger Reserve in 2012. Monkeys from Karnataka might have entered Tamil Nadu carrying the virus or infected ticks. Subsequently, KFD in monkeys was reported in Kerala state in 2014 and Goa and Maharashtra states in 2016. Substantial overlap occurred between reported monkey deaths and human cases of KFD (Figure 2). We identified the drivers behind KFD transmission and geographic expansion based on the literature (Table 2).

Higher mortality rates occurred among S. entellus monkeys (81% of 1,159 deaths) than among M. radiata monkeys during 1957–1964 (7). Most monkey deaths were reported in evergreen and semievergreen forests in the Western Ghats (8). We found no other information associating the frequency of monkey deaths to habitat.

The abundance of these primate species in the area of interest is difficult to determine because of limited studies with inconsistent sampling methods. In Karnataka, higher encounter rates with M. radiata monkeys were reported in wet evergreen forests and human-inhabited areas (9). M. radiata monkeys were encountered mainly in the Western Ghats and the Southern Plateau, whereas S. entellus monkeys were abundant in the Western Ghats and Northern Plains. Based on a 2001 Environmenta Information System bulletin (10), the national population of M. radiata monkeys in India was ≈150,000 and that of S. entellus monkeys was ≈300,000. Both species have suffered population decline because of habitat loss, translocation, and hunting, and minimal efforts have been undertaken to conserve these species (9,11).

Conclusions

Our study highlights the need for consistent surveillance of monkey deaths. Monkey deaths caused by KFDV are harbingers of human cases (1,3,4), making these animals potential sentinels for KFD (6). Therefore, determining these primate species’ relative susceptibility to KFDV to evaluate the potential to use monkey deaths for surveillance is essential. In laboratory experiments, higher mortality rates have been reported in S. entellus than M. radiata monkeys (12). Patil et al. (13) experimentally infected M. radiata monkeys with KFDV and found that only 20% of these primates had onset of severe clinical signs, but all exhibited viral shedding and a humoral immune response. Thus, other factors might contribute to KFD mortality rates under natural conditions, and M. radiata monkeys might be less susceptible to KFD than previously thought. KFDV infection can often be subclinical in nature, explaining why fewer deaths have been observed for M. radiata than S. entellus monkeys. By shedding the virus through body secretions, M. radiata monkeys might aid in expanding KFDV into new areas. This phenomenon underscores the need for conducting serum or fecal surveillance of primates to determine KFDV epidemiology and transmission.

Most human cases of KFD are typically reported during December–May, the same period during which monkey deaths generally occur. Local public health authorities often undertake precautionary measures on the basis of monkey deaths, including spraying acaricide around areas with monkey carcasses and vaccination of persons within a 5-km radius (6,14). The importance of animals as sentinels of infectious diseases, environmental hazards, and acts of bioterrorism is well documented (15). Because monkey deaths are used as sentinels for KFD, establishing year-round surveillance systems that consistently report KFD-related monkey deaths by date, location, and species is essential to better understand the epidemiology of the disease and design appropriate public health measures.

One limitation of our review is the inconsistency and gaps in the availability of reported monkey deaths caused by KFD. Few studies report monkey mortality data or provide specific monkey deaths by location, year, and species, so assessing whether mortality rates have changed over time is difficult. Another limitation is the incomplete data on testing and diagnoses of monkey carcasses for KFDV because of challenges such as distance to the testing site and delays in discovery.

Further research is needed to develop serosurveys specific to KFDV among monkeys, determine species-specific vulnerability to KFDV, and assess whether KFDV can spread through routes other than tick transmission. Testing capacity in KFD-endemic states should be strengthened to conduct timely monkey necropsies, providing more information on the prevalence of KFD in these sentinel animals, to elucidate the epidemiology of KFDV and protect monkey and human health.

Ms. Chakraborty is a doctoral candidate in the Program in Ecology Evolution and Conservation Biology at the University of Illinois, Urbana–Champaign. Her research interests include the ecology and epidemiology of vectorborne diseases and One Health approaches in disease surveillance and prevention.

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Acknowledgment

Funding for this study was obtained through the University of Illinois Campus Research Board and was supported by the Cooperative State Research, Education, and Extension Service of the US Department of Agriculture (project no. ILLU 875-952).

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References

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Figures
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Cite This Article

DOI: 10.3201/eid2707.210463

Original Publication Date: June 12, 2021

Table of Contents – Volume 27, Number 7—July 2021

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William Sander, University of Illinois Urbana–Champaign, 1008 W Hazelwood Dr, Urbana, IL 61802, USA

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Page created: May 21, 2021
Page updated: June 17, 2021
Page reviewed: June 17, 2021
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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