Research Article
Prevalence and Associated Risk Factors of Bovine Ephemeral Fever in the Cattle of Nageshwari Upazila, Kurigram, Bangladesh
Md. Kamruzzaman Akimul1*, Md. Abdullah Al Mamun2, Md. Imran Hossen3
1Department of Microbiology and Public Health, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Babuganj-8210, Barishal, Bangladesh; 2Department of Pathology and Parasitology, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Babuganj-8210, Barishal, Bangladesh; 3Department of Anatomy and Histology, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Babuganj-8210, Barishal, Bangladesh.
Abstract | The Bovine Ephemeral Fever (BEF) is a viral disease transmitted by vectors among the cattle, which causes serious economic losses in the tropical and sub-tropical areas. This cross-sectional study aimed to estimate the prevalence of BEF and identify risk factors among cattle in Nageshwari Upazila, Kurigram District, Bangladesh. A clinical examination of 280 cattle that are of diverse age grouping, sex, and breed was done in January to April 2025. Structured questionnaires were used to collect information on different categories. The prevalence rates of BEF were 7.86% in total: the highest prevalence occurred in January (12.5%) and gradually decreased until April (2.86%), which are in agreement with the existence of seasonal patterns depending on the activity of the vectors. The highest prevalence in accordance to age was in cattle aged between 1 to 3 years (10.17%) and above 5 years (9.52%). There was greater prevalence in Male (9.68%) than in Female (7.34%) and in local breeds (8.64%) than in crossbreeds (5%). Nevertheless, all these differences were not of a statistical significance (p > 0.05). These findings suggest BEF occurrence is more influenced by environmental and vector-related factors than by age, sex, or breed. The results will give significant baseline epidemiological data that would present a guide to future research and control plans in Bangladesh.
Keywords | Bovine ephemeral fever (BEF), Prevalence, Risk factors, Cattle, Kurigram, Bangladesh
Editor | Muhammad Nauman Zahid, Quality Operations Laboratory, University of Veterinary and Animal Sciences, Lahore, Pakistan.
Received | August 15, 2025; Accepted | November 10, 2025; Published | December 19, 2025
*Correspondence | Md. Kamruzzaman Akimul, Department of Microbiology and Public Health, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Babuganj-8210, Barishal, Bangladesh; Email: [email protected]
Citation | Akimul MK, Al-Mamun MA, Hossen MI (2026). Prevalence and associated risk factors of bovine ephemeral fever in the cattle of Nageshwari Upazila, Kurigram, Bangladesh. S. Asian J. Life Sci. 14: 01-06.
DOI | https://dx.doi.org/10.17582/journal.sajls/2026/14.01.06
ISSN (Online) | 2307-8316; ISSN (Print) | 2309-3331
Copyright © 2026 Akimul et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
INTRODUCTION
Bovine Ephemeral Fever (BEF), also called as three-day sickness is a viral disease of cattle and buffaloes in areas with subtropical and tropical climates (Akakpo, 2015). It is considered an acute tropical disease and important economically. The Bovine Ephemeral Fever Virus (BEFV) which is of the genus Ephemerovirus in family Rhabdoviridae causes it. BEFV virion is a bullet-shaped, slightly tapered at one end envelope that is normally between 70 nm in diameter (60-80 nm), 145 nm in length (120-170 nm) (Holmes and Doherty, 1970; Gubala et al., 2008). Clinical signs that are more or less consistent with this disease include sudden onset of high fever, muscle stiffness, lameness, decreased feed intake, and clinical signs that normally persist up to three days. BEF has a low case fatality rate but produces significant economic losses because of the reduced milk yield, temporary infertility, interference with labor, and high susceptibility to secondary infections (Walker and Klement, 2015).
It is spread through blood-feeding arthropods, especially mosquitos (Culex spp.) and biting midges (Culicoides spp.) and a common outbreak takes place during a time that there is a higher activity by the spreading arthropod (Davies and Walker, 1974). Infected animals may show fever up to 41.5 oC, nasal discharge, shaking of the muscles, and recumbency of pain in the joint and muscle. Specifically, in high producing dairy cows, complications occur, most prominently mastitis, pneumonia, and reproductive complications (Radostits et al., 2007; OIE, 2021).
BEF has been described in Africa, the Middle East, Asia and northern Australia, with a seasonal pattern related to climatic conditions that favour the proliferation of vectors (OIE, 2021). In Asia, outbreaks have generated significant effects on the economies of, among others, India, China, Japan, and Thailand. Within the past years, researchers have discussed the effects of climate change and environmental changes shifting geographic range of insect vectors, which may result in the extended global distribution of BEF (Samy and Peterson, 2016).
In a situation like Bangladesh where the national population of cattle is approximated to be around 24 million (DLS, 2023), BEF becomes a hidden menace to livestock productivity. However, despite cases of sporadic BEF-like cases being detected, especially during monsoon and post-monsoon phases (Samy and Christley, 2018). Other factors such as poor disease surveillance, absence of molecular diagnostic systems, and regular misdiagnosis of the disease with other febrile diseases can be used. As the country relies on the cattle to produce dairy, draft power and provides income in rural areas, more consideration to BEF should be paid to handle the disease and retains financial sustainability.
Objectives of the study
To assess the epidemiological characteristics of Bovine Ephemeral Fever (BEF) among cattle in selected regions of Bangladesh.
MATERIALS AND METHODS
Study area and population
The study will be conducted on the Nageshwari Upazila of Kurigram District of Bangladesh from January to April, 2025, in areas with a large population density of cattle (Figure 1). A total population of 280 cattle will take part in the study.
Diagnosis of bovine ephemeral fever
A tentative diagnosis of BEF is primarily based on clinical signs, epidemiological data and seasonal occurrence. According to Akakpo (2015) key indicators include:
Data collection
Clinical observation on cattle will observe symptoms of Bovine Ephemeral Fever (BEF) such as fever, stiffness in the muscles, lameness, recumbence, and decreased feeding. An epidemiological questioner will be used to obtain information on the possible risk factors, including age, breed, sex, history of vaccination and recent contact with insect vectors (Walker and Klement, 2015).
Data analysis
Raw data were coded and entered into Microsoft excel in order to analyze the data. Clinical cases and related risk factor distributions were summarized based on the use of descriptive statistics. The association between categorical variables was determined using chi-square tests, whereas the independent predictors of BEF infection were determined using logistic. The study map was prepared with the help of ArcGIS tools. A p-value < 0.05 will be considered statistically significant.
RESULTS
Table 1 and Figure 2 provides the prevalence of Bovine Ephemeral Fever (BEF) in cattle on a monthly basis with a total prevalence of 7.86 (22/280). The highest prevalence was always recorded in January (12.50%), and February (10%), whereas the lowest prevalence was observed in April (2.86%).
Table 1: Monthly prevalence of bovine ephemeral fever (BEF) in cattle.
|
Month |
Total population |
Positive cases |
Prevalence (%) |
|
Overall prevalence |
280 |
22 |
7.86% |
|
January prevalence |
64 |
8 |
12.50% |
|
February prevalence |
80 |
8 |
10% |
|
March prevalence |
66 |
4 |
6.06% |
|
April prevalence |
70 |
2 |
2.86% |
Table 2: Overall prevalence of bovine ephemeral fever (BEF) by different categories.
|
Category |
Sub category |
Total population |
Positive cases |
Prevalence (%) |
Chi-square test |
P value |
|
Overall Prevalence |
280 |
22 |
7.86% |
|||
|
Age categories |
<1 year |
45 |
1 |
2.22% |
3.22 |
0.36 |
|
1-3years |
118 |
12 |
10.17% |
|||
|
3-5years |
54 |
3 |
5.56% |
|||
|
>5 years |
63 |
6 |
9.52% |
|||
|
Sex categories |
Male |
62 |
6 |
9.68% |
0.303 |
0.582 |
|
Female |
218 |
16 |
7.34% |
|||
|
Breed categories |
Local |
220 |
19 |
8.64% |
0.748 |
0.387 |
|
Cross |
60 |
3 |
5% |
|||
In Table 2, the prevalence of Bovine Ephemeral Fever (BEF) in cattle under various categories, with a total prevalence of 7.86% (22/280). The rates between and within age groups (2.22-10.17%), sexes (male 9.68% vs. female 7.34%), and breeds (local 8.64% vs. crossbred 5%), though not significantly different (p > 0.05).
As shown in Table 3, BEF had a prevalence of 12.5% (8/64) in January compared with the total prevalence of 7.86. The most prevalence was seen in cattle older than 5 years (23.53%), 1-3 years old (12.5%), and none in the calves under 1-year-old and cattle between 3-5 years old. Practical differences in prevalence by age, sex, and breed were not found to be significant (p > 0.05).
Table 3: BEF Prevalence in January by different categories.
|
Category |
Sub category |
Total population |
Positive cases |
Prevalence (%) |
Chi-square test |
P value |
|
January prevalence |
64 |
8 |
12.5% |
|||
|
Age categories |
<1 year |
8 |
0 |
0% |
3.52 |
0.318 |
|
1-3years |
32 |
4 |
12.5% |
|||
|
3-5years |
7 |
0 |
0% |
|||
|
>5 years |
17 |
4 |
23.53% |
|||
|
Sex categories |
Male |
18 |
3 |
16.67% |
0.044 |
0.834 |
|
Female |
46 |
5 |
10.87% |
|||
|
Breed categories |
Local |
43 |
6 |
13.95% |
0.0101 |
0.920 |
|
Cross |
21 |
2 |
9.52% |
|||
Table 4: BEF prevalence in February by different categories.
|
Category |
Sub category |
Total population |
Positive cases |
Prevalence (%) |
Chi Square test |
P value |
|
February prevalence |
80 |
8 |
10% |
|||
|
Age categories |
<1 year |
16 |
1 |
6.25% |
1.79 |
0.617 |
|
1-3years |
36 |
5 |
13.89% |
|||
|
3-5years |
10 |
0 |
0% |
|||
|
>5 years |
18 |
2 |
11.11% |
|||
|
Sex categories |
Male |
18 |
2 |
11.11% |
0.028 |
0.866 |
|
Female |
62 |
6 |
9.68% |
|||
|
Breed categories |
Local |
56 |
7 |
12.5% |
1.17 |
0.279 |
|
Cross |
24 |
1 |
4.17% |
|||
Table 4 reveals that in February, the prevalence of Bovine Ephemeral Fever (BEF) stood at 10% (8/80), which was marginally above the total prevalence of 7.86%. Cattle of age 1-3 years (13.89%), >5 years (11.11%), and <1 year (6.25%) showed the highest prevalence, with no cases recorded in the 3-5 years’ age group. Variations in prevalence among age, sex, and breed were not statistically pronounced (p > 0.05).
Table 5 shows the prevalence of Bovine Ephemeral Fever (BEF) in March and the total prevalence was 6.06% (4/66), lower than the total prevalence of 7.86%. The highest prevalence was found in cattle aged 35 years (11.76%), then aged between 13 years (8.70%), and none in cattle older than 5 years and calves younger than 1 year. The prevalence differences by age, sex, and breed category were not significant (p > 0.05).
Table 6 illustrates the prevalence of the Bovine Ephemeral Fever (BEF) in April with a total prevalence of 2.86 (2/70), the least prevalence compared to the other four months. The most prevalence was in cattle of the age 3-5 years (5%), 1-3 years (3.70%), and none in calves below 1 year of age or cattle older than 5 years. The age, sex, and breed differences in prevalence were not significant (p > 0.05).
Table 5: BEF prevalence in March by different categories.
|
Category |
Sub category |
Total population |
Positive cases |
Prevalence (%) |
Chi-Square test |
P value |
|
March Prevalence |
66 |
4 |
6.06% |
|||
|
Age categories |
<1 year |
13 |
0 |
0% |
2.75 |
0.432 |
|
1-3years |
23 |
2 |
8.70% |
|||
|
3-5years |
17 |
2 |
11.76% |
|||
|
>5 years |
13 |
0 |
0% |
|||
|
Sex categories |
Male |
12 |
1 |
8.33% |
0.115 |
0.734 |
|
Female |
54 |
3 |
5.56% |
|||
|
Breed categories |
Local |
56 |
4 |
7.14% |
0.705 |
0.401 |
|
Cross |
10 |
0 |
0% |
|||
Table 6: BEF prevalence in April by different categories.
|
Category |
Sub category |
Total population |
Positive cases |
Prevalence (%) |
Chi square test |
P value |
|
April prevalence |
70 |
2 |
2.86% |
|||
|
Age categories |
<1 year |
8 |
0 |
0% |
1.04 |
0.791 |
|
1-3years |
27 |
1 |
3.70% |
|||
|
3-5years |
20 |
1 |
5% |
|||
|
>5 years |
15 |
0 |
0% |
|||
|
Sex categories |
Male |
14 |
0 |
0% |
0.496 |
0.481 |
|
Female |
56 |
2 |
3.57% |
|||
|
Breed categories |
Local |
65 |
2 |
3.08% |
0.153 |
0.696 |
|
Cross |
5 |
0 |
0% |
|||
DISCUSSION
The present study focused on the monthly and categorical Bovine Ephemeral Fever (BEF) prevalence in cattle in Nageshwari Upazila, Kurigram District, Bangladesh. The overall prevalence during the four-month period from January to April, 2025 was 7.86%. In comparison, Nadeem et al. (2024) reported a higher seroprevalence of 18.33%. The overall highest rate of monthly prevalence in the current research was in January (12.50%), February (10%), March (6.06%), and April (2.86%) (Table 1 and Figure 2). That is comparatively lower than Liao et al. (1998) (13.6%) and higher than Hossain (2021) (4.54%). Such a decline indicates that there might be some seasonal factor affecting the disease transmission since the rates were higher in the cooler and probably more humid months, conditions that may suit the activities of these insect vectors that transmit BEF.
Age-wise categorization showed that age group 1-3 years of age recorded the highest overall prevalence (10.17%), age group over 5 years the second highest (9.52%), whereas calves with age of less than 1 year bore the lowest prevalence (2.22%) (p = 0.36) (Table 2). Similarly, Nadeem et al. (2024) detected the presence of BEFV in 20%, 96.97%, and 75% of cattle aged <1 year, 2-3 years, and >3 years, respectively (P = 0.00001). Based on sex-wise prevalence, it was observed that the overall prevalence in male cattle was slightly higher (9.68%) compared to female cattle (7.34%) (p = 0.582) (Table 2). This observation is contrary to that of Nadeem et al. (2024) who found females to have a higher seroprevalence (67.59%) than males (58.33%). This finding is consistent with the results of Zaghawa et al. (2016), who reported a significantly higher seropositive rate in males (24.4%) than in females (14.6%). Breed wise analysis indicated that there was a high prevalence of local breeds (4.64%) compared to crossbreeds (5%) (p = 0.387) (Table 2). This observation is inconsistent with the data of Nadeem et al. (2024) showing higher seroprevalence among crossbreeds (70%) in comparison with the local breed (45%). Although, indigenous cattle may be thought of as more resistant to the indigenous diseases, the high local frequency may indicate greater exposure based on less intensive management and housing of local breeds as compared to crossbred animals.
In January, the largest age-specific prevalence was apparent in cattle of >5 years (23.53%). The prevalence among the males (16.67%) was higher than that among the females (10.87%), whereas the local breeds (13.95%) were more prevalent than crossbreed (9.52%) (Table 3). In February, Cattle age 1-3 years had the greatest age-specific prevalence (13.89%), whereas none of the observations belonged to the 3-5 years age category. There was slight male (11.11%) prevalence compared to female (9.68%) with local breeds (12.5%) being affected more as compared to crossbreeds (4.17) (Table 4). In March, the highest age-specific prevalence was observed in the 3–5 years age group (11.76%), followed by the 1–3 years group (8.70%). No cases have been observed in the < 1 year and the > 5 years groups. The prevalence was slightly greater in males (8.33%) than females (5.56%) and local breeds (7.14%) were the only affected one (Table 5). In April, the highest age-specific prevalence was in the 3–5 years group (5%), followed by 1–3 years (3.70%), with no cases in <1 year or >5 years. Positive cases were confined to the females (3.57%) and all affected were local breeds (3.08%) (Table 6). But there were no significant differences (P > 0.05).
BEF is endemic and seasonally affected in the region, although its prevalence differed by age, sex, and breed but not significantly. A stronger focus on vector control, increased surveillance in summer months, and augmented studies on environmental and weather dynamics are suggested to minimise the effects of the disease on livestock health.
CONCLUSIONS
BEF has been found to occur among cattle in the study area with an overall prevalence rate of 7.86%. The greatest prevalence was reported in the month of January, which should be a seasonal pattern. Though age, sex and breed exhibited some variation in terms of infection, no significant associations were observed. The results highlight the importance of strategic surveillance and vector control during seasons of the year when the risks of the disease are high in order to reduce its impacts.
Limitations
The study limitations are that the clinical and serological cases are not confirmed with a molecular test, the sample size used in stratified analysis is not very large and the study takes into consideration a single upazila which may not be generalizable. Nonetheless, this study contributes valuable baseline data on BEF epidemiology in northern Bangladesh.
Acknowledgments
The authors would like to express their sincere appreciation to the Upazila Livestock Officer and all staff of the Upazila Livestock Office and Veterinary Hospital, Nageshwari, Kurigram, as well as to the local farmers and veterinary personnel of Nageshwari Upazila, Kurigram, for their valuable support during the fieldwork.
Novelty Statement
This study provides the first baseline report on the prevalence and associated risk factors of BEF in cattle in Nageshwari Upazila, Kurigram, Bangladesh. The findings highlight the seasonal occurrence of BEF and offer essential epidemiological data to support future disease surveillance and control strategies.
Author’s Contribution
Data collection: MKA, MAAM. Data analysis: MKA, MAAM. Writing the original draft: MKA, MIH. Review and editing: MKA. All authors read and approved the final manuscript.
Funding statement
This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors and was conducted voluntarily.
Generative AI and AI-assisted technology statement
The authors declare that no generative AI tools were used for data collection, analysis, or conclusions in this paper. AI was used only for improving language and grammar. The authors take full responsibility for the content of the article.
Conflict of interest
The authors have declared no conflict of interest.
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