Serosurveillance and Postvaccination Seromonitoring of Peste Des Petits Ruminants in Small Ruminants in Central Gondar Zone, Northwest Ethiopia

IF 2.6 2区 农林科学 Q2 INFECTIOUS DISEASES
Firdyawukal Abuhay Tafere, Mastewal Birhan Atanaw, Enyiew Alemnew Alamerew, Melkie Dagnaw Fenta, Genetu Kassahun Berie, Kefale Ambachew Shiferaw, Bemrew Admassu Mengistu, Anmaw Shite Abat
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引用次数: 0

Abstract

Peste des petits ruminants (PPR) is a highly contagious transboundary viral disease of small ruminants caused by the PPR virus (PPRV). Despite Ethiopia’s goal of eradicating PPR by 2027 through a risk-based vaccination strategy, the disease remains endemic, with 554 outbreaks reported nationwide. This cross-sectional study was conducted in the North Gondar Zone, Ethiopia, between June 2024 and February 2025 to evaluate antibody responses in vaccinated small ruminants and estimate PPRV seroprevalence in unvaccinated flocks. A multistage cluster sampling design was used to select the study sites, while individual animals were selected using a haphazard sampling approach to approximate random sampling. A total of 600 serum samples were collected, including 300 from vaccinated and 300 from unvaccinated small ruminants; samples from vaccinated animals were obtained ~28 days postvaccination. All samples were tested for anti-PPRV antibodies using competitive enzyme-linked immunosorbent assay (c-ELISA). Overall individual-level seropositivity in the vaccinated population was 75%, comprising 75.73% in sheep and 72.1% in goats, serving as a proxy measure of flock immunity. In unvaccinated animals, PPRV seroprevalence was 14.33% (95% confidence interval [CI]: 10.6%–18.82%). Multivariable logistic regression identified age and flock size as the main risk factors influencing seropositivity. Adult animals were 2.89 times as likely to be seropositive as young animals (95% CI: 1.17–7.15; p = 0.022), and animals in medium-sized flocks were more likely to test positive than those in small flocks (AOR = 2.26; 95% CI: 1.11–4.63; p = 0.026). No significant differences were observed across districts, species, sex, production systems, newly introduced animals, or animal movement (p  > 0.05). The observed seropositivity was slightly below the commonly used 80% population immunity target associated with reducing transmission under the PPR eradication framework. The detection of PPRV antibodies in unvaccinated animals indicates previous exposure to PPRV and highlights the need for strengthened surveillance to assess whether active virus circulation persists in the area. To achieve effective control and eventual eradication of PPR, intensified vaccination programs combined with active surveillance are needed. Furthermore, refining vaccination strategies in alignment with global and national eradication plans is essential to establish PPR-free zones in these districts.

埃塞俄比亚西北部冈达尔中部地区小反刍动物中小反刍兽疫血清监测和疫苗接种后血清监测
小反刍兽疫是由小反刍兽疫病毒(PPRV)引起的小反刍动物高度传染性跨界病毒性疾病。尽管埃塞俄比亚的目标是通过基于风险的疫苗接种战略,到2027年根除小反刍兽疫,但该疾病仍然是地方性的,全国报告了554起疫情。这项横断面研究于2024年6月至2025年2月在埃塞俄比亚北贡达尔地区进行,目的是评估接种疫苗的小反刍动物的抗体反应,并估计未接种疫苗的畜群中PPRV的血清流行率。采用多阶段整群抽样设计选择研究地点,采用随机抽样方法选择动物个体,近似随机抽样。共采集血清样本600份,其中接种疫苗的小反刍动物300份,未接种疫苗的小反刍动物300份;接种疫苗后约28天采集动物标本。所有样品均采用竞争性酶联免疫吸附试验(c-ELISA)检测抗pprv抗体。在接种疫苗的人群中,总体个体水平血清阳性为75%,其中绵羊为75.73%,山羊为72.1%,可作为群体免疫力的替代指标。在未接种疫苗的动物中,PPRV血清阳性率为14.33%(95%可信区间[CI]: 10.6%-18.82%)。多变量logistic回归确定年龄和畜群大小是影响血清阳性的主要危险因素。成年动物血清阳性的可能性是幼畜的2.89倍(95% CI: 1.17-7.15; p = 0.022),中型畜群的动物比小型畜群的动物更容易检测出阳性(AOR = 2.26; 95% CI: 1.11-4.63; p = 0.026)。不同地区、物种、性别、生产系统、新引进动物或动物运动间无显著差异(p < 0.05)。观察到的血清阳性略低于根除小反刍兽疫框架下常用的与减少传播相关的80%人群免疫目标。在未接种疫苗的动物中检测到PPRV抗体表明曾接触过PPRV,并强调需要加强监测,以评估该地区是否继续存在活跃的病毒传播。为实现有效控制并最终根除小反刍兽疫,需要加强疫苗接种规划并结合积极监测。此外,根据全球和国家根除计划完善疫苗接种战略对于在这些地区建立无小反刍兽疫区至关重要。
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来源期刊
Transboundary and Emerging Diseases
Transboundary and Emerging Diseases 农林科学-传染病学
CiteScore
8.90
自引率
9.30%
发文量
350
审稿时长
1 months
期刊介绍: Transboundary and Emerging Diseases brings together in one place the latest research on infectious diseases considered to hold the greatest economic threat to animals and humans worldwide. The journal provides a venue for global research on their diagnosis, prevention and management, and for papers on public health, pathogenesis, epidemiology, statistical modeling, diagnostics, biosecurity issues, genomics, vaccine development and rapid communication of new outbreaks. Papers should include timely research approaches using state-of-the-art technologies. The editors encourage papers adopting a science-based approach on socio-economic and environmental factors influencing the management of the bio-security threat posed by these diseases, including risk analysis and disease spread modeling. Preference will be given to communications focusing on novel science-based approaches to controlling transboundary and emerging diseases. The following topics are generally considered out-of-scope, but decisions are made on a case-by-case basis (for example, studies on cryptic wildlife populations, and those on potential species extinctions): Pathogen discovery: a common pathogen newly recognised in a specific country, or a new pathogen or genetic sequence for which there is little context about — or insights regarding — its emergence or spread. Prevalence estimation surveys and risk factor studies based on survey (rather than longitudinal) methodology, except when such studies are unique. Surveys of knowledge, attitudes and practices are within scope. Diagnostic test development if not accompanied by robust sensitivity and specificity estimation from field studies. Studies focused only on laboratory methods in which relevance to disease emergence and spread is not obvious or can not be inferred (“pure research” type studies). Narrative literature reviews which do not generate new knowledge. Systematic and scoping reviews, and meta-analyses are within scope.
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