Pathobiological characterization and estimation of the basic reproduction number of a recombinant african swine fever virus in contact-exposed pigs in Vietnam
The Viet Hoang Nguyen , Ngoc Duong Vu , Viet Dung Nguyen , Thi Tam Than , Thuy Nga Dang , Huu Thien Nguyen , Thi Chau Giang Tran , Hoai Thuong Nguyen , Phuong Anh Nguyen , Ki-Hyun Cho , Seong-Keun Hong , Aruna Ambagala , Yeon-Hee Kim , Van Phan Le
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Abstract
African swine fever virus (ASFV) causes a highly lethal disease in domestic pigs, resulting in severe economic losses. This study examined the clinical course, viral dynamics, immune response, and pathological changes in pigs infected with a recombinant ASFV strain of p72 genotypes I/II (rASFV I/II) via direct inoculation or natural contact. The directly infected pig developed persistent fever (> 40 °C), anorexia, lethargy, and respiratory distress soon after the onset of viremia, and died six days post-inoculation (dpi). Contact-exposed pigs showed similar clinical signs and died between 12 and 21 days post-exposure (dpe). Real-time PCR revealed rapid viral replication in blood and secretions, with peak viral loads detected at or just before death. No detectable antibody response was observed in either group, indicating acute disease progression and high virulence. Gross pathological examination revealed severe lesions in the spleen, lymph nodes, gastrointestinal tract, and lungs. Epidemiological analysis using the susceptible–infectious–removed (SIR) model estimated the generation time (mean ± SD) as 1.101 ± 0.507 days. The basic reproduction number (R₀) was 1.201 (95% CI: 0.628–2.302) using the exponential growth method and 1.248 (95% CI: 0.310–3.236) using the maximum likelihood method. These findings demonstrate the high virulence and transmission potential of the rASFV I/II strain, highlighting the need for early detection and rapid containment measures.
期刊介绍:
Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal.
Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge.
Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.