Pathogenic Potential of Erysipelothrix piscisicarius in Pigs and Its Implications for Surveillance in Brazil

IF 3 2区 农林科学 Q2 INFECTIOUS DISEASES
Fernando Moreira Petri, Giovana da Silva Nogueira, Gustavo M. R. Simão, Ana K. Panneitz, Gabriel A. de Aguiar, Ana Clara A. de Lima, Eduarda R. Braga, Kellem do Carmo, Suzana S. Kuchiishi, Adrienny T. Reis, Fabio A. Vannucci, Luís Guilherme de Oliveira
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引用次数: 0

Abstract

Erysipelothrix (E.) piscisicarius is an emerging pathogen previously described in fish and more recently isolated from a clinical outbreak in swine. This study aimed to evaluate the course of infection and pathological outcomes of E. piscisicarius in pigs using an experimental intradermal challenge model. Twenty-six 70-day-old pigs were randomly allocated into three groups: high-dose (HD group, n = 10) and low-dose (LD group, n = 10) were challenged intradermally with 1010 colony forming units (CFUs) and 108 CFU using a Brazilian field isolate obtained from a pig with erysipelas-like lesions and confirmed by whole-genome sequencing (WGS) and average nucleotide identity (ANI), respectively, while CONT (control, n = 6) served as a negative control. Clinical monitoring, hematological assessments, acute-phase proteins (APPs) quantification, bacteriological culture, and quantitative PCR (qPCR) targeting the spaC gene were performed over 14 days. Challenged pigs developed mild clinical signs, including transient fever and characteristic rhomboid skin lesions resembling classical swine erysipelas. No mortality occurred. Hematological analysis revealed significant reductions in red blood cell (RBC) count, hemoglobin (HGB), and hematocrit (HCT), particularly in the LD group at 7 and 14 days post-challenge (dpc) (p  < 0.05), suggestive of inflammatory anemia. APP analysis showed a significant increase in ceruloplasmin across all groups over time, whereas transferrin levels decreased only in the control group. Bacterial isolation was unsuccessful; however, qPCR detected E. piscisicarius deoxyribonucleic acid (DNA) in blood, skin, liver, and spleen samples, confirming systemic dissemination, particularly at 7 dpc. These findings demonstrate that E. piscisicarius can induce clinical and pathological alterations in swine, although with mild severity under experimental conditions. Moreover, the study highlights the importance of differentiating E. piscisicarius from E. rhusiopathiae in diagnostics, given the potential limitations of current vaccine strategies.

Abstract Image

猪瘟丹毒在猪中的致病潜力及其对巴西监测的意义
猪瘟丹毒(E.)是一种新出现的病原体,以前在鱼类中发现,最近从猪的临床暴发中分离出来。本研究旨在通过实验性皮内感染模型来评估猪肉苁苁菌的感染过程和病理结果。将26头70日龄的猪随机分为三组:高剂量组(HD组,n = 10)和低剂量组(LD组,n = 10),分别用1010个菌落形成单位(CFU)和108个菌落形成单位(CFU)进行皮内注射,使用的是从患有丹毒样病变的猪身上获得的巴西野外分离物,并通过全基因组测序(WGS)和平均核苷酸鉴定(ANI)确认,而CONT(对照组,n = 6)作为阴性对照。在14天内进行临床监测、血液学评估、急性期蛋白(APPs)定量、细菌学培养和靶向spaC基因的定量PCR (qPCR)。感染猪出现轻度临床症状,包括短暂发热和典型的菱形皮肤病变,类似于典型的猪丹毒。无死亡发生。血液学分析显示,红细胞(RBC)计数、血红蛋白(HGB)和红细胞压积(HCT)显著降低,特别是在LD组在攻击后7天和14天(dpc) (p < 0.05),提示炎症性贫血。APP分析显示,随着时间的推移,所有组的铜蓝蛋白水平都显著增加,而转铁蛋白水平仅在对照组下降。细菌分离不成功;然而,qPCR在血液、皮肤、肝脏和脾脏样本中检测到piscisicarius脱氧核糖核酸(DNA),证实了全身传播,特别是在第7天。这些结果表明,尽管在实验条件下的严重程度较轻,但piscisicarius可引起猪的临床和病理改变。此外,考虑到当前疫苗策略的潜在局限性,该研究强调了在诊断中区分piscisicarius与rhusiopathiae的重要性。
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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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