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.
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.
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 Wuque. 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.
Table 1.
ASFV status and genotype distribution in Asia (updated November 2025).
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.
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