Prevalence of classical swine fever, African swine fever, and Japanese encephalitis: a multi-disease study in Indian pigs

Main Article Content

Neha Naik
Jagadish Hiremath
Chethan Kumar H.B
Vijay M
Mouna.V
Akshatha Velankar
Manjunatha J
K. P. Suresh
N. Shivasharanappa
Sharanagouda Patil
B.R. Gulati

Abstract

The health of swine populations is increasingly threatened by diseases such as classical swine fever (CSF), African swine fever (ASF), and Japanese encephalitis (JE), which causeeconomic losses. This study investigated the seroprevalence and distribution of these pathogens across 13 districts in Chhattisgarh, Madhya Pradesh, and Telangana, India. A total of 345 serum samples and 275 whole blood samples were collected for various diagnostic testing. Samples were analyzed using reverse transcriptase polymerase chain reaction (RT-PCR), virus neutralization test (VNT), and indirect enzyme-linked immunosorbent assay (iELISA), with CSF showing the highest seroprevalence in Chhattisgarh (76.63%), while ASF waslowest (7.21%). In Madhya Pradesh, the CSF seroprevalence was 33.33%, with no ASF detected. JE positivity was 12.37% in Chhattisgarh and 44.44% in Madhya Pradesh. RT-PCR of 275 whole blood samples from Telangana revealed 11.27% positivity for CSF and 9.45% for JE, with no ASF cases. In Chhattisgarh, 7.20% of the samples showed concurrent antibody positivity for both CSF and ASF. Additionally, 2.06% were positive for CSF, ASF, and JE, indicating concurrent exposure to multiple pathogens. Age-wise analysis showed the highest CSF positivity among older pigs in Chhattisgarh and Madhya Pradesh, with higher rates observed in pigs >2 years. These findings emphasize the necessity of antigen and antibody testing for effective swine disease surveillance, revealing concurrent exposure to multiple pathogens. A combined approach using serological and molecular diagnostics strengthens surveillance, supports multi-disease control strategies, and is vital for limiting disease spread and maintaining swine health.

Keywords:
Classical swine fever, Concurrent exposure, Disease surveillance, Seroprevalence, Swine diseases

Article Details

References

Guo X, Zhang M, Liu X, Zhang Y, Wang C, Guo Y. Attachment, entry, and intracellular trafficking of classical swine fever virus. Viruses. 2023;15(9):1870. doi: 10.3390/v15091870. DOI: https://doi.org/10.3390/v15091870

Patil SS, Suresh KP, Hemadri D, Hiremath J, Sridevi R, Krishnamoorthy P, et al. Spatial seroprevalence of classical swine fever in India. Tropical Animal Health and Production. 2021;53(3):389. doi: 10.1007/s11250-021-02829-6. DOI: https://doi.org/10.1007/s11250-021-02829-6

Sapre SK, Moghe RG, Bhagwat SV, Chaudhry PG, Purobit BL. A note on observations and investigations into an outbreak of swine fever in Bombay (Maharashtra). Indian Veterinary Journal.1962;39:527–534.

World Organisation for Animal Health. WOAH Terrestrial Manual, Chapter 3.9.1. African swine fever (Infection with African swine fever virus). WOAH. 2024. https://www.woah.org/fileadmin/Home/fr/Health_standards/tahm/3.09.01_ASF.pdf

Guinat C, Gogin A, Blome S, Keil G, Pollin R, Pfeiffer DU, et al. Transmission routes of African swine fever virus to domestic pigs: current knowledge and future research directions. Veterinary Record. 2016;178(11):262–267. doi: 10.1136/vr.103593. DOI: https://doi.org/10.1136/vr.103593

Patil SS, Suresh KP, Vashist V, Prajapati A, Pattnaik B, Roy P. African swine fever: a permanent threat to Indian pigs. Veterinary World. 2020;13(10):2275–2285. doi: 10.14202/vetworld.2020.2275-2285. DOI: https://doi.org/10.14202/vetworld.2020.2275-2285

Erlanger TE, Weiss S, Keiser J, Utzinger J, Wiedenmayer K. Past, present, and future of Japanese encephalitis. Emerging Infectious Diseases. 2009;15(1):1–7. doi: 10.3201/eid1501.080311. DOI: https://doi.org/10.3201/eid1501.080311

Dhanalakshmi M, Dhanze H, Bhilegaonkar KN, Mote A, Gupta I, Agri H, et al. Seroprevalence of Japanese encephalitis virus in pig populations of Tamil Nadu, India: Exploring the tropical endemic link of virus. Comparative Immunology, Microbiology and Infectious Diseases. 2024;110:102189. doi: 10.1016/j.cimid.2024.102189. DOI: https://doi.org/10.1016/j.cimid.2024.102189

Namachivayam V, Umayal K. Proceedings of National Conference on Japanese Encephalitis. New Delhi:Indian Council of Medical Research. 1982:30–33.

Gulati BR, Singha H, Singh BK, Virmani N, Khurana SK, Singh RK. Serosurveillance for Japanese encephalitis virus infection among equines in India. Journal of Veterinary Science. 2011;12(4):341–345. doi: 10.4142/jvs.2011.12.4.341. DOI: https://doi.org/10.4142/jvs.2011.12.4.341

World Organisation for Animal Health. WOAH Terrestrial Manual, Chapter 3.1.10. Japanese encephalitis. WOAH. 2021. https://www.woah.org/fileadmin/Home/fr/Health_standards/tahm/3.01.10_JEV.pdf

Sergeant ESG. Epitools Epidemiological Calculators. Australia:Ausvet. 2018. http://epitools.ausvet.com.au

Patil SS, Hemadri D, Shankar BP, Raghavendra AG, Veeresh H, Sindhoora B, et al. Genetic typing of recent classical swine fever isolates from India. Veterinary Microbiology. 2010;141(3–4):367–373. doi: 10.1016/j.vetmic.2009.09.021. DOI: https://doi.org/10.1016/j.vetmic.2009.09.021

Paton DJ, McGoldrick A, Greiser-Wilke I, Parchariyanon S, Song J-Y, Liou PP, et al. Genetic typing of classical swine fever virus. Veterinary Microbiology. 2000;73(2–3):137–157. doi: 10.1016/S0378-1135(00)00141-3. DOI: https://doi.org/10.1016/S0378-1135(00)00141-3

Agüero M, Fernández J, Romero L, Sánchez Mascaraque C, Arias M, Sánchez-Vizcaíno JM. Highly sensitive PCR assay for routine diagnosis of African swine fever virus in clinical samples. Journal of Clinical Microbiology. 2003;41(9):4431–4434. doi: 10.1128/JCM.41.9.4431-4434.2003. DOI: https://doi.org/10.1128/JCM.41.9.4431-4434.2003

Bharucha T, Sengvilaipaseuth O, Vongsouvath M, Vongsouvath M, Davong V, Panyanouvong P, et al. Development of an improved RT-qPCR Assay for detection of Japanese encephalitis virus (JEV) RNA including a systematic review and comprehensive comparison with published methods. PloS ONE. 2018;13(3): e0194412. doi: 10.1371/journal.pone.0194412. DOI: https://doi.org/10.1371/journal.pone.0194412

Zeng Z, Liu Z, Wang W, Tang D, Liang H, Liu Z. Establishment and application of a multiplex PCR for rapid and simultaneous detection of six viruses in swine. Journal of Virological Methods. 2014;208:102–106. doi: 10.1016/j.jviromet.2014.08.001. DOI: https://doi.org/10.1016/j.jviromet.2014.08.001

Jiang Y, Shang H, Xu H, Zhu L, Chen W, Zhao L, et al. Simultaneous detection of porcine circovirus type 2, classical swine fever virus, porcine parvovirus and porcine reproductive and respiratory syndrome virus in pigs by multiplex polymerase chain reaction. The Veterinary Journal. 2010;183(2):172–175. doi: 10.1016/j.tvjl.2008.11.016. DOI: https://doi.org/10.1016/j.tvjl.2008.11.016

Moennig V. The control of classical swine fever in wild boar. Frontiers in Microbiology. 2015;6:1211. doi: 10.3389/fmicb.2015.01211. DOI: https://doi.org/10.3389/fmicb.2015.01211

Li Y-C, Chiou M-T, Lin C-N. Serodynamic analysis of the piglets born from sows vaccinated with modified live vaccine or E2 subunit vaccine for classical swine fever. Pathogens. 2020;9(6):427. doi: 10.3390/pathogens9060427. DOI: https://doi.org/10.3390/pathogens9060427

Kleiboeker SB. Swine fever: classical swine fever and African swine fever. Veterinary Clinics of North America: Food Animal Practice. 2002;18(3):431–451. doi: 10.1016/s0749-0720(02)00028-2. DOI: https://doi.org/10.1016/S0749-0720(02)00028-2

Paton DJ, Greiser-Wilke I. Classical swine fever–an update. Research in Veterinary Science. 2003;75(3):169–178. doi: 10.1016/s0034-5288(03)00076-6. DOI: https://doi.org/10.1016/S0034-5288(03)00076-6

Chenais E, Depner K, Guberti V, Dietze K, Viltrop A, Ståhl K. Epidemiological considerations on African swine fever in Europe 2014–2018. Porcine Health Management. 2019;5(1):6. doi: 10.1186/s40813-018-0109-2. DOI: https://doi.org/10.1186/s40813-018-0109-2

Oliveira ARS, Cohnstaedt LW, Noronha LE, Mitzel D, McVey DS, Cernicchiaro N. Perspectives regarding the risk of introduction of the Japanese encephalitis virus (JEV) in the United States. Frontiers in Veterinary Science. 2020;7:48. doi: 10.3389/fvets.2020.00048. DOI: https://doi.org/10.3389/fvets.2020.00048

Raut AA, Aasdev A, Mishra A, Dutta B, Bharali A, Konwar N, et al. Detection of coinfection of a divergent subgroup of genotype I Japanese encephalitis virus in multiple classical swine fever virus outbreaks in pigs of Assam, India. Transboundary and Emerging Diseases. 2021;68(4):2622–2627. doi: 10.1111/tbed.13903. DOI: https://doi.org/10.1111/tbed.13903