Comparative infectivity and horizontal transmission ability of the isolates PCV2a, PCV2b, and PCV2d

IF 2.4 2区 农林科学 Q3 MICROBIOLOGY Veterinary microbiology Pub Date : 2024-08-06 DOI:10.1016/j.vetmic.2024.110214
Chong Yu , Mengxiang Cao , Yanwu Wei, Hao Zhang, Jianhang Liu, Li Feng, Liping Huang
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Abstract

Porcine circovirus type 2 (PCV2) causes postweaning multisystemic wasting syndrome in piglets. Differences in the infectivity and horizontal transmissibility of different isolates of PCV2a, PCV2b, and PCV2d in pigs were evaluated by HE and IHC staining, PCR, virus titration, and IPMA to determine their clinical symptoms, pathological changes, levels of virus and antibody, and cohabitation infectivity. In the cohabitation infection experiment, weak viremia and low levels of antibodies were detected in the pigs challenged with PCV2a-CL, whereas no viremia or antibodies were detected in the corresponding cohabiting pigs. Furthermore, no PCV2 was isolated from any organ of pigs that were challenged with PCV2a-CL, as well as from those of their cohabiting pigs. In contrast, persistent viremia and pathological changes, including swollen inguinal lymph nodes, were detected in both the challenged and cohabiting pigs after PCV2b-BY or PCV2d-LNHC infection. Alive PCV2 was detected in the tonsils, inguinal lymph nodes, spleen, and kidneys of the experimental pigs by virus titration, and the highest viral titer was detected in the tonsils, followed by the inguinal lymph nodes. In a comparative analysis of the challenged and cohabiting pigs, a 1-week delay in viremia and specific antibodies was observed in the cohabiting pigs. Moreover, the number of viruses isolated from the tonsils and inguinal lymph nodes of the pigs cohabiting with PCV2d-LNHC-challenged pigs was significantly greater than those in the pigs that were directly challenged with PCV2d-LNHC in cohabitation infection experiment (P<0.05). Together, these results indicated that the infectivity and horizontal transmissibility of the strains PCV2b-BY and PCV2d-LNHC were much greater than those of the strain PCV2a-CL and provided some insights into PCV2 pathogenicity.

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PCV2a、PCV2b 和 PCV2d 分离物的传染性和水平传播能力比较。
猪圆环病毒 2 型(PCV2)会导致仔猪断奶后多系统消瘦综合征。通过 HE 和 IHC 染色、PCR、病毒滴定和 IPMA 评估了 PCV2a、PCV2b 和 PCV2d 不同分离株在猪体内的感染性和水平传播性差异,以确定它们的临床症状、病理变化、病毒和抗体水平以及同居感染性。在同居感染实验中,接受 PCV2a-CL 挑战的猪体内检测到微弱的病毒血症和低水平的抗体,而相应的同居猪体内未检测到病毒血症或抗体。此外,从感染 PCV2a-CL 的猪及其同群猪的任何器官中都没有分离到 PCV2。相反,在感染 PCV2b-BY 或 PCV2d-LNHC 后,受感染猪和同居猪体内都检测到了持续的病毒血症和病理变化,包括腹股沟淋巴结肿大。通过病毒滴定法,在实验猪的扁桃体、腹股沟淋巴结、脾脏和肾脏中检测到了存活的 PCV2,在扁桃体中检测到的病毒滴度最高,其次是腹股沟淋巴结。对实验猪和同居猪进行比较分析后发现,同居猪的病毒血症和特异性抗体延迟了 1 周。此外,在同居感染实验中,与 PCV2d-LNHC 感染猪同居的猪的扁桃体和腹股沟淋巴结中分离到的病毒数量明显多于直接感染 PCV2d-LNHC 的猪(P<0.05)。
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来源期刊
Veterinary microbiology
Veterinary microbiology 农林科学-兽医学
CiteScore
5.90
自引率
6.10%
发文量
221
审稿时长
52 days
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.
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