Immunological Assessment of Veterinary Infectious Diseases

A special issue of Veterinary Sciences (ISSN 2306-7381). This special issue belongs to the section "Veterinary Microbiology, Parasitology and Immunology".

Deadline for manuscript submissions: 10 January 2025 | Viewed by 5920

Special Issue Editors


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Guest Editor
Department of Animal Health, University of León, 24071 León, Spain
Interests: veterinary pathology; microbiology; porcine respiratory disease complex; antimicrobial resistance; vaccines; immune response; immunohistochemistry

E-Mail Website
Guest Editor
Department of Animal Health, University of León, 24071 León, Spain
Interests: veterinary pathology; microbiology; porcine respiratory disease complex; antimicrobial resistance; vaccines; immune response; immunohistochemistry
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Guest Editor
Department of Animal Health, Universidad de León, León, Spain
Interests: antimicrobial resistance; biofilm; microbiology; porcine respiratory disease complex; vaccination
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Infectious diseases are responsible for large economic losses in farm animals, pets, and wildlife. Most of these diseases are contagious, and they result in high animal mortality and morbidity associated with reduced animal growth, treatment costs, and condemnation in organs and carcasses at the slaughterhouse. Moreover, zoonotic diseases represent a danger to human health. The diagnosis of infectious diseases is mainly based on serological tests and cultures of the causative pathogens. Histopathological studies with routine staining or histochemical techniques may also help to identify some pathogens and/or their tissue injury. However, these tools have limitations such as difficulties in interpreting serological results in immunocompromised animals, the unavailability of fresh tissue for culture, and non-specific tissue lesions, among others. In this context, the aim of this Special Issue is to encourage scientists to publish their immunological studies on any infectious disease in animals to better understand the host–pathogen relationships that allow for the improvement and development of novel prophylactic, therapeutic and diagnostic tools.

Prof. Dr. María José García-Iglesias
Prof. Dr. César-B. Gutiérrez Martín
Dr. Sonia Martinez
Guest Editors

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Keywords

  • immunological assessment
  • infectious diseases
  • animals

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Published Papers (3 papers)

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Research

13 pages, 1812 KiB  
Article
Detection of Serum IgG Specific for Brachyspira pilosicoli and “Brachyspira canis” in Dogs
by Julia Gothe, Matthias Horn, Christoph G. Baums, Romy M. Heilmann and Wieland Schrödl
Vet. Sci. 2024, 11(7), 302; https://doi.org/10.3390/vetsci11070302 - 3 Jul 2024
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Abstract
Brachyspira pilosicoli (B. pilosicoli) is a pathogen in pigs, poultry, and humans causing colitis, diarrhea, and poor growth rates. Its role as a canine pathogen is controversial, and the seroprevalence of specific IgG antibodies against B. pilosicoli in dogs is unknown. [...] Read more.
Brachyspira pilosicoli (B. pilosicoli) is a pathogen in pigs, poultry, and humans causing colitis, diarrhea, and poor growth rates. Its role as a canine pathogen is controversial, and the seroprevalence of specific IgG antibodies against B. pilosicoli in dogs is unknown. A further, not yet officially recognized Brachyspira species in dogs is “Brachyspira canis” (“B. canis“), which is proposed to be apathogenic. This study evaluates enzyme-linked immunosorbent assays (ELISAs) measuring serum IgG antibodies specific for B. pilosicoli or “B. canis” and investigates levels of specific IgG antibodies against B. pilosicoli and “B. canis” in a cohort of clinical patients presented at an animal referral clinic. These ELISAs use detergent-extracted antigens from B. pilosicoli and “B. canis”. To increase analytic specificity, we precipitated the antigens with trichloroacetic acid (TCA) to isolate and concentrate the respective protein fraction. Our results indicate that a large number of serum IgG antibodies bind to shared epitopes of detergent-extracted antigens of the two spirochaetes. Our data also suggest that dogs might not only carry B. pilosicoli but also have “B. canis”-specific serum IgG antibodies. Full article
(This article belongs to the Special Issue Immunological Assessment of Veterinary Infectious Diseases)
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15 pages, 5934 KiB  
Article
Identification, Genetic Characterization, and Pathogenicity of Three Feline Herpesvirus Type 1 Isolates from Domestic Cats in China
by Mingliang Deng, Haiyang Liang, Yue Xu, Qiwen Shi, Fang Bao, Caiying Mei, Zhihong Dai and Xianhui Huang
Vet. Sci. 2024, 11(7), 285; https://doi.org/10.3390/vetsci11070285 - 25 Jun 2024
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Abstract
(1) Background: Feline herpesvirus (FHV-1) is a significant pathogen in cats, causing respiratory and ocular diseases with consequential economic and welfare implications. (2) Methods: This study aimed to isolate and characterize FHV-1 from clinical samples and assess its pathogenicity. We collected 35 nasal [...] Read more.
(1) Background: Feline herpesvirus (FHV-1) is a significant pathogen in cats, causing respiratory and ocular diseases with consequential economic and welfare implications. (2) Methods: This study aimed to isolate and characterize FHV-1 from clinical samples and assess its pathogenicity. We collected 35 nasal and ocular swabs from cats showing symptoms of upper respiratory tract infection and FHV positivity detected by polymerase chain reaction (PCR). Viral isolation was carried out using feline kidney (F81) cell lines. Confirmation of FHV-1 presence was achieved through PCR detection, sequencing, electron microscopy, and indirect immunofluorescence assay. The isolated strains were further characterized by evaluating their titers, growth kinetics, and genetic characteristics. Additionally, we assessed the pathogenicity of the isolated strains in a feline model, monitoring clinical signs, viral shedding, and histopathological changes. (3) Results: Three strains of FHV-1 were isolated, purified, and identified. The isolated FHV-1 strains exhibited high homology among themselves and with domestic isolates and FHV-1 viruses from around the world. However, they showed varying degrees of virulence, with one strain (FHV-A1) causing severe clinical signs and histopathological lesions. (4) Conclusion: This study advances our understanding of the genetic and pathogenic characteristics of FHV-1 in China. These findings underscore FHV-A1 isolate as a potentially ideal candidate for establishing a challenge model and as a potential vaccine strain for vaccine development. Full article
(This article belongs to the Special Issue Immunological Assessment of Veterinary Infectious Diseases)
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11 pages, 864 KiB  
Article
An ELISA to Detect Antibodies to Bovine Alphaherpesviruses 1 and 5 and Bubaline Alphaherpesvirus 1 in Cattle Sera
by Camila Mengue Scheffer, Sylio Alfredo Petzhold, Ana Paula Muterle Varela, Willian Pinto Paim, Phelipe Magalhães Duarte, Márcia Regina Loiko, Cristine Cerva, Candice Schmidt, Adrieli Wendlant, Samuel Paulo Cibulski, Diane Alves de Lima, Caroline Tochetto, Anne Caroline Ramos dos Santos, Juliana Inês Herpich, Thais Fumaco Teixeira, Helton Fernandes dos Santos, Fabrício Souza Campos, Ana Cláudia Franco and Paulo Michel Roehe
Vet. Sci. 2023, 10(2), 110; https://doi.org/10.3390/vetsci10020110 - 2 Feb 2023
Cited by 2 | Viewed by 2217
Abstract
Bovine alphaherpesvirus 1 (subtypes 1.1, 1.2a, and 1.2b), type 5 (subtypes 5a, 5b, and 5c), and bubaline herpesvirus 1 (BuHV-1) induce highly, though not fully cross-reactive serological responses. Most types and subtypes of these viruses circulate particularly in countries of the southern hemisphere, [...] Read more.
Bovine alphaherpesvirus 1 (subtypes 1.1, 1.2a, and 1.2b), type 5 (subtypes 5a, 5b, and 5c), and bubaline herpesvirus 1 (BuHV-1) induce highly, though not fully cross-reactive serological responses. Most types and subtypes of these viruses circulate particularly in countries of the southern hemisphere, notably Brazil and Argentina. Therefore, the detection of infected animals is important in defining prevention and control strategies, particularly when flocks are destined for international trade. Identification of infected herds is most often achieved by assays that detect antibodies, such as enzyme immunoassays (ELISAs). However, to date, no ELISA has been evaluated in its capacity to detect antibodies to these alphaherpesviruses. Here, an ELISA was developed to detect antibodies to all currently recognized BoAHV-1, BoAHV-5, and BuAHV-1 types/subtypes, and its sensitivity and specificity were determined. Six hundred bovine sera were screened in serum neutralization tests (SN) against the seven viruses. ELISAs prepared with each of the viruses were compared to SN. Subsequently, a combined assay with multiple antigens LISA was prepared by mixing five viral antigens, chosen for their highest sensitivity in the preparative assays. In comparison to SN, the mAgELISA sensitivity was 96.5% with 96.1% specificity (κ = 0.93; PPV = 95.0%; NPV = 97.3%). The findings reveal that the mAgELISA developed here is highly suitable for the detection of antibodies, comparable in sensitivity and specificity to that of SN when performed with all known types and subtypes of bovine and bubaline alphaherpesviruses. Full article
(This article belongs to the Special Issue Immunological Assessment of Veterinary Infectious Diseases)
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