Next Article in Journal
Complete Genome Sequences of Human Japanese Encephalitis Virus Genotype V Isolates in Korea Reveal Genotype-Specific Amino Acid Signatures
Previous Article in Journal
Advances in Human Metapneumovirus Research: Clinical Impact, Diagnostic Innovations, and Therapeutic Challenges
Previous Article in Special Issue
In Vitro Influenza A Virus-Inactivating Activity of HIDROX®, Hydroxytyrosol-Rich Aqueous Olive Pulp Extract
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

The Evolving Threat of African Swine Fever in Asia

by
Wen-Hung Wang
1,2,
Arunee Thitithanyanont
3 and
Sheng-Fan Wang
1,4,5,6,*
1
Center for Tropical Medicine and Infectious Disease, Kaohsiung Medical University, Kaohsiung 80708, Taiwan
2
School of Medicine, College of Medicine, National Sun Yat-Sen University, Kaohsiung 804201, Taiwan
3
Department of Microbiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand
4
Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, Kaohsiung 80708, Taiwan
5
M.Sc. Program in Tropical Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan
6
Department of Medical Research, Kaohsiung Medical University Hospital, Kaohsiung 80708, Taiwan
*
Author to whom correspondence should be addressed.
Pathogens 2025, 14(12), 1278; https://doi.org/10.3390/pathogens14121278
Submission received: 3 December 2025 / Revised: 9 December 2025 / Accepted: 10 December 2025 / Published: 12 December 2025
(This article belongs to the Collection Emerging and Re-emerging Pathogens)

1. Introduction

Originally identified in Kenya in 1921, African swine fever (ASF) primarily remained a sub-Saharan concern for nearly a century [1]. However, its disastrous introduction into East Asia via China in 2018 fundamentally altered the global swine production landscape [2]. Over the past seven years, the region has undergone a profound epidemiological shift: what began as an acute, invading panzootic has transitioned into a state of chronic, deeply entrenched endemicity.
In retrospect, this transition was a predictable consequence of the virus’s formidable biological makeup. As the sole member of the Asfarviridae family, African swine fever virus (ASFV) is a genetically complex, large double-stranded DNA virus. Its resilience is derived from an intricate, multilayered icosahedral morphology, incorporating an internal lipid membrane and an outer envelope hijacked from the host cell [3], which confers extraordinary environmental tenacity. ASFV can withstand broad pH and temperature ranges and retain infectivity for months in contaminated fomites, feed, or soil, and even longer in frozen pork products [4].
This durability underpins complex transmission networks that are notoriously difficult to disrupt, necessitating a multilayered defense strategy. While direct contact is the primary route of transmission, indirect routes such as contaminated vehicles, equipment, personnel, and infectious swill feeding play a critical role [5]. Consequently, strict on-farm biosecurity, controlled animal and human movements, and the proper disposal and sterilization of food waste (particularly from international carriers) are essential in order to disrupt these networks (Figure 1). Furthermore, in specific ecological niches, sylvatic cycles involving Ornithodoros ticks act as long-term biological reservoirs [6]. Combined with a genome encoding numerous proteins that subvert host innate immunity, ASFV is uniquely suited for long-term persistence. Therefore, disease surveillance and efficient early detection through laboratory tests are indispensable (Figure 1). Asia is now facing the arduous reality of managing a resident, highly adaptable pathogen established across diverse ecological and production niches, where strict quarantine protocols and rapid stamping out remain the final lines of defense.

2. When the Last Barrier Breaks: The Breach of Taiwan

While widespread ASFV incursions have been reported across the region, for several years, Japan and Taiwan were the only East Asian nations to remain officially ASF-free. Japan has maintained historical freedom from the virus without any reported outbreaks. Regrettably, Taiwan lost its ASF-free status in October 2025 following a confirmed outbreak at a farm in Wuqi District. This detection, officially reported to the World Organisation for Animal Health (WOAH), represents a critical turning point for disease control in the region [7,8].
Taiwan was previously a regional anomaly, maintaining disease-free status despite close proximity to endemic neighbors and dense trade and travel links. This status was sustained through what was arguably one of the world’s most aggressive border enforcement regimes [9]; under a “zero-tolerance” policy, Taiwan implemented 100% X-ray screening of hand luggage from high-risk areas, immediate heavy fines (upwards of USD 6500) for travelers carrying undeclared pork products, and a decisive nationwide ban on the traditional practice of swill feeding to pigs. The successful incursion of the virus despite these measures underscores the difficulty of maintaining absolute exclusion against such a resilient pathogen in the long term.

3. From Virulent Waves to Silent Carriers

The antagonist in this ongoing crisis is not a static entity. In long-standing endemic zones, selective pressures on ASFV are shifting. While highly virulent genotype II strains remain dominant, the epidemiological picture has become increasingly blurred (Table 1). Historical experience indicates that in endemic regions, naturally attenuated strains may emerge over time, leading to chronic or subclinical infections that evade standard diagnostic and clinical surveillance protocols [10]. These less dramatic infections can quietly maintain transmission in systems where biosecurity is insufficient.
This natural evolution is now being aggressively accelerated by human intervention. Driven by economic pressure and desperation, the unlawful use of unapproved live-attenuated vaccines has yielded serious and sometimes disastrous consequences. Recent surveillance has detected vaccine-escape mutants and, most alarmingly, recombinant strains harboring genetic characteristics of both genotype I and II viruses [11].
Since 2021, novel genotype I/II recombinant strains have emerged in China and have subsequently spread to Northern Vietnam [12]. These viruses possess a unique and deceptive profile: they retain the lethal virulence of genotype II (including the CD2v gene, a key virulence factor in ASFV) while utilizing the genotype I backbone to evade protection from current genotype II-based vaccines [11]. Furthermore, these novel strains often manifest atypical or muted clinical signs, creating populations of “silent carriers” that facilitate viral movement through trade chains and production networks. This stealthy propagation undermines passive surveillance systems that rely heavily on mortality or classical clinical presentation as early warning signals.

4. The Illusion of a Quick Vaccine Fix

The increasing complexity of field strains underscores a critical danger: the industry’s hope for an immediate “vaccine savior.” The scientific obstacles to developing a safe, effective ASFV vaccine are immense. Natural infection does not reliably induce classical neutralizing antibodies, and correlates of protection remain poorly defined due to the virus’s complex immunomodulatory mechanisms [13]. While legitimate progress toward licensed live-attenuated vaccines has occurred in some nations [14], achieving a universally safe, genetically stable, and DIVA-compliant (Differentiating Infected from Vaccinated Animals) product suitable for widespread, largely unsupervised field use presents unprecedented challenges [13].
In this context, premature deployment of imperfect biologicals in an already complex epidemiological environment is not a solution; it acts as an accelerant for confusion and risk. Overreliance on a future technological fix also risks breeding complacency around the only defense currently proven effective against this environmentally stable virus: rigorous, consistently applied biosecurity along the entire production and value chain [15].

5. Conclusions

The consolidation of ASF endemicity across Asia serves as a stark reminder that, against such a biologically resilient pathogen, “zero-risk” zones are likely to be temporary. The region must transition from an “exclusion mindset” to preparing for a multi-decade course of disease management. The path forward necessitates a strategic realignment grounded in scientific reality. Governments must prioritize transparent genomic and epidemiological surveillance to track viral evolution and detect emergent variants. The industry must accept that modernization, compartmentalization, and rigorous biosecurity segregation are now baseline requirements for continuing production in an endemic environment. Until the complex immunological hurdles of ASFV are fully overcome to produce a truly safe, effective, and DIVA-compliant vaccine, biosecurity resilience will remain the primary form of protection between the swine industry and recurrent waves of devastating production losses.

Author Contributions

S.-F.W.: Writing—Original Draft Preparation, Writing—Review and Editing. W.-H.W.: Data Curation, Formal Analysis, Writing—Review and Editing. A.T.: Writing—Original Draft Preparation, Writing—Review and Editing. S.-F.W.: Conceptualization, Methodology, Writing—Review and Editing. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by grants from the National Science and Technology Council, R.O.C. (NSTC 112-2320-B-037-032-MY3, NSTC 113-2740-M-037-001 and NSTC 112-2740-M-037-001), the Kaohsiung Medical University Research Center (KMU-TC114B01), the Kaohsiung Medical University Research Foundation (KMU-M112007), the NYCU-KMU Joint Research Project (NYCU-KMU-113-I004), and the NSYSU-KMU Joint Research Project (#NSYSUKMU 113-I04).

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Penrith, M.L.; Vosloo, W.; Jori, F.; Bastos, A.D. African swine fever virus eradication in Africa. Virus Res. 2013, 173, 228–246. [Google Scholar] [CrossRef] [PubMed]
  2. Zhou, X.; Li, N.; Luo, Y.; Liu, Y.; Miao, F.; Chen, T.; Zhang, S.; Cao, P.; Li, X.; Tian, K.; et al. Emergence of African Swine Fever in China, 2018. Transbound. Emerg. Dis. 2018, 65, 1482–1484. [Google Scholar] [CrossRef] [PubMed]
  3. Gaudreault, N.N.; Madden, D.W.; Wilson, W.C.; Trujillo, J.D.; Richt, J.A. African Swine Fever Virus: An Emerging DNA Arbovirus. Front. Vet. Sci. 2020, 7, 215. [Google Scholar] [CrossRef] [PubMed]
  4. Mazur-Panasiuk, N.; Zmudzki, J.; Wozniakowski, G. African Swine Fever Virus—Persistence in Different Environmental Conditions and the Possibility of its Indirect Transmission. J. Vet. Res. 2019, 63, 303–310. [Google Scholar] [CrossRef] [PubMed]
  5. Guinat, C.; Gogin, A.; Blome, S.; Keil, G.; Pollin, R.; Pfeiffer, D.U.; Dixon, L. Transmission routes of African swine fever virus to domestic pigs: Current knowledge and future research directions. Vet. Rec. 2016, 178, 262–267. [Google Scholar] [CrossRef] [PubMed]
  6. Arzumanyan, H.; Hakobyan, S.; Avagyan, H.; Izmailyan, R.; Nersisyan, N.; Karalyan, Z. Possibility of long-term survival of African swine fever virus in natural conditions. Vet. World 2021, 14, 854–859. [Google Scholar] [CrossRef] [PubMed]
  7. World Organzation for Animal Health. WOAH Confirms First ASF Case in Taiwan. 2025. Available online: https://wahis.woah.org/#/in-review/6933 (accessed on 1 December 2025).
  8. African Swine Fever (ASF) Situation Update in Asia & Pacific Food and Agriculture Organization of the United Nations. 2025. Available online: https://www.fao.org/animal-health/situation-updates/asf-in-asia-pacific (accessed on 3 December 2025).
  9. Wang, W.H.; Lin, C.Y.; Chang Ishcol, M.R.; Urbina, A.N.; Assavalapsakul, W.; Thitithanyanont, A.; Lu, P.L.; Chen, Y.H.; Wang, S.F. Detection of African swine fever virus in pork products brought to Taiwan by travellers. Emerg. Microbes Infect. 2019, 8, 1000–1002. [Google Scholar] [CrossRef] [PubMed]
  10. Ito, S.; Bosch, J.; Martinez-Aviles, M.; Sanchez-Vizcaino, J.M. The Evolution of African Swine Fever in China: A Global Threat? Front. Vet. Sci. 2022, 9, 828498. [Google Scholar] [CrossRef] [PubMed]
  11. Zhao, D.; Sun, E.; Huang, L.; Ding, L.; Zhu, Y.; Zhang, J.; Shen, D.; Zhang, X.; Zhang, Z.; Ren, T.; et al. Highly lethal genotype I and II recombinant African swine fever viruses detected in pigs. Nat. Commun. 2023, 14, 3096. [Google Scholar] [CrossRef] [PubMed]
  12. Le, V.P.; Nguyen, V.T.; Le, T.B.; Mai, N.T.A.; Nguyen, V.D.; Than, T.T.; Lai, T.N.H.; Cho, K.H.; Hong, S.K.; Kim, Y.H.; et al. Detection of Recombinant African Swine Fever Virus Strains of p72 Genotypes I and II in Domestic Pigs, Vietnam, 2023. Emerg. Infect. Dis 2024, 30, 991–994. [Google Scholar] [CrossRef] [PubMed]
  13. Revilla, Y.; Perez-Nunez, D.; Richt, J.A. African Swine Fever Virus Biology and Vaccine Approaches. Adv. Virus Res. 2018, 100, 41–74. [Google Scholar] [PubMed]
  14. Tran, X.H.; Phuong, L.T.T.; Huy, N.Q.; Thuy, D.T.; Nguyen, V.D.; Quang, P.H.; Ngon, Q.V.; Rai, A.; Gay, C.G.; Gladue, D.P.; et al. Evaluation of the Safety Profile of the ASFV Vaccine Candidate ASFV-G-DeltaI177L. Viruses 2022, 14, 896. [Google Scholar] [CrossRef] [PubMed]
  15. Gallardo, M.C.; Reoyo, A.T.; Fernandez-Pinero, J.; Iglesias, I.; Munoz, M.J.; Arias, M.L. African swine fever: A global view of the current challenge. Porc. Health Manag. 2015, 1, 21. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The diagram illustrates a multi-faceted approach to preventing viral introduction and limiting spread within swine populations. Key strategies include strict border control and quarantine protocols, management of food waste (swill) from international sources, rigorous on-farm biosecurity, active disease surveillance, and rapid response mechanisms such as stamping out.
Figure 1. The diagram illustrates a multi-faceted approach to preventing viral introduction and limiting spread within swine populations. Key strategies include strict border control and quarantine protocols, management of food waste (swill) from international sources, rigorous on-farm biosecurity, active disease surveillance, and rapid response mechanisms such as stamping out.
Pathogens 14 01278 g001
Table 1. ASFV status and genotype distribution in Asia (updated November 2025).
Table 1. ASFV status and genotype distribution in Asia (updated November 2025).
CountrySeverity/StatusCirculating GenotypeRemarks
ChinaWidespread/EndemicGenotype I/II RecombinantSource of diverse viral strains including the highly virulent recombinant (I/II) variant.
VietnamWidespreadGenotype II RecombinantRecombinant strains (I/II) confirmed in Northern provinces; poses high risk of regional spread.
TaiwanLocal OutbreakGenotype I/II
Recombinant
The first confirmed domestic ASF outbreak occurred in October 2025 at a large pig farm in Wuqi District. According to the Ministry of Agriculture (MOA), the outbreak-associated strain exhibits high similarity to strains currently found in China and Vietnam.
PhilippinesRegional/ActiveGenotype IIPersistence in multiple provinces; spread driven by movement of contaminated pork products.
South KoreaSporadicGenotype IICases mostly confined to wild boar populations; farm outbreaks remain sporadic and contained.
ThailandEndemicGenotype IIWidespread distribution since initial detection in 2022.
LaosEndemicGenotype IIHigh risk of cross-border transmission due to porous borders with endemic neighbors.
CambodiaEndemicGenotype IISporadic outbreaks continue to be reported.
IndiaActive SpreadGenotype IIOutbreaks concentrated in Northeast India with signs of spread to other regions.
IndonesiaRegionalGenotype IIOutbreaks reported in major islands including Sumatra and Java.
MalaysiaRegionalGenotype IICases present in both Peninsular Malaysia and Borneo (Sabah/Sarawak).
Note: Taiwan’s status has been updated following the WOAH confirmation of the first local outbreak on 25 October 2025. The viral strain detected in Taiwan is highly similar to the genotype I/II recombinant strains currently endemic in China and Northern Vietnam.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Wang, W.-H.; Thitithanyanont, A.; Wang, S.-F. The Evolving Threat of African Swine Fever in Asia. Pathogens 2025, 14, 1278. https://doi.org/10.3390/pathogens14121278

AMA Style

Wang W-H, Thitithanyanont A, Wang S-F. The Evolving Threat of African Swine Fever in Asia. Pathogens. 2025; 14(12):1278. https://doi.org/10.3390/pathogens14121278

Chicago/Turabian Style

Wang, Wen-Hung, Arunee Thitithanyanont, and Sheng-Fan Wang. 2025. "The Evolving Threat of African Swine Fever in Asia" Pathogens 14, no. 12: 1278. https://doi.org/10.3390/pathogens14121278

APA Style

Wang, W.-H., Thitithanyanont, A., & Wang, S.-F. (2025). The Evolving Threat of African Swine Fever in Asia. Pathogens, 14(12), 1278. https://doi.org/10.3390/pathogens14121278

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop