Lianne G. Eertink , Megan Swope , Tirth Uprety , Chithra Sreenivasan , Allen E. Page , Emma N. Adam , Dan Wang , Feng Li
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引用次数: 0
Abstract
Equine rotavirus A (ERVA) can cause foal diarrhoea and the most common ERVA genotypes are G3P[12] and G14P[12]. Since the introduction of a monovalent killed G3P[12] vaccine, infection in neonates has decreased. We aimed to determine the dynamics and longevity of maternally derived anti-G3P[12] neutralizing antibodies (NAbs) in foals and what, if any, cross-reactivity exists between maternally derived NAbs against G14P[12]. Serum samples were collected from 50 mare-foal pairs before each vaccination and up to 6 months post-foaling for mares and up to 7 months of age for foals. These samples were then used for virus-neutralization antibody assays with both G3P[12] and G14P[12] viruses. We observed that vaccination of mares could increase their serum NAb titers. Pre-nursing serum samples of foals collected at birth before the first nursing contained no detectable NAbs. In contrast, post-nursing serum samples of foals showed a significant amount of NAb levels, thereby confirming that these NAbs are passed through the mare’s colostrum. Our study demonstrated that there is variation in the ratio of NAbs transferred from the serum of mares to the serum of their foals. Results also confirmed evidence of cross-reactivity between maternal antibodies in the serum of G3P[12] vaccinated dams and G14P[12]. Heterologous (G14P[12]) NAb titers were about 2- to 4-fold lower than homologous (G3P[12]) titers in colostrum, milk, and serum samples of both mares and their foals. Our data demonstrate that G3 and G14 NAbs in the serum of foals decreased steadily over time with the lowest point measured at approximately 4 months of age.
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.