4.4 Article

Pathogenicity of an African swine fever virus strain isolated in Vietnam and alternative diagnostic specimens for early detection of viral infection

期刊

PORCINE HEALTH MANAGEMENT
卷 7, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s40813-021-00215-0

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African swine fever; Vietnam; Pathogenicity; Incubation period; Clinical signs; Virus excretion pattern; Alternative diagnostic specimen

资金

  1. Cooperative Research Program for Agriculture Science and Technology Development (Project title: Analysis and monitoring of clinical and epidemiological features of African swine fever), Rural Development Administration, Republic of Korea [PJ01484301]

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The study investigated the pathogenicity of ASFV isolates from Vietnam and explored alternative sampling methods for early detection. The results showed that the ASFV strain was peracute to acute form, and a rope-based oral fluid collection method could be useful for early detection, while ear tissue samples might be a simple alternative specimen for diagnosing ASF infection in dead pigs.
Background African swine fever (ASF), caused by the ASF virus (ASFV), was first reported in Vietnam in 2019 and spread rapidly thereafter. Better insights into ASFV characteristics and early detection by surveillance could help control its spread. However, the pathogenicity and methods for early detection of ASFV isolates from Vietnam have not been established. Therefore, we investigated the pathogenicity of ASFV and explored alternative sampling methods for early detection. Results Ten pigs were intramuscularly inoculated with an ASFV strain from Vietnam (titer, 10(3.5) HAD(50)/mL), and their temperature, clinical signs, and virus excretion patterns were recorded. In addition, herd and environmental samples were collected daily. The pigs died 5-8 days-post-inoculation (dpi), and the incubation period was 3.7 +/- 0.5 dpi. ASFV genome was first detected in the blood (2.2 +/- 0.8) and then in rectal (3.1 +/- 0.7), nasal (3.2 +/- 0.4), and oral (3.6 +/- 0.7 dpi) swab samples. ASFV was detected in oral fluid samples collected using a chewed rope from 3 dpi. The liver showed the highest viral loads, and ear tissue also exhibited high viral loads among 11 tissues obtained from dead pigs. Overall, ASFV from Vietnam was classified as peracute to acute form. The rope-based oral fluid collection method could be useful for early ASFV detection and allows successful ASF surveillance in large pig farms. Furthermore, ear tissue samples might be a simple alternative specimen for diagnosing ASF infection in dead pigs. Conclusions Our data provide valuable insights into the characteristics of a typical ASFV strain isolated in Vietnam and suggest an alternative, non-invasive specimen collection strategy for early detection.

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