1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Foot-and-mouth disease virus O/ME-SA/Ind 2001 lineage outbreak in vaccinated Holstein Friesian cattle in Saudi Arabia in 2016

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background: Foot-and-mouth disease virus (FMDV) is a highly contagious viral infection of large ruminants. Despite the massive application of vaccines against FMDV, several outbreaks are still being reported in Africa and Asia.

          Aim: To perform molecular characterization of FMDV in an outbreak among a cattle herd Saudi Arabia in 2016. This herd had been vaccinated with a polyvalent FMDV vaccine.

          Methods: To investigate this outbreak, we collected specimens from 77 animals showing typical clinical signs of FMDV. Specimens including sera, nasal swabs, and tissues (tongue, coronary bands, hooves, and hearts) were collected. We tested the collected cattle sera for the presence of FMDV antibodies with commercial ELISA kits. In addition, we tested the swabs for the presence of the most common FMDV strains (O, A, Asia-1 and SAT-2) with RT-PCR using serotype-specific oligonucleotides.

          Results: Serology showed that 22% of the tested sera were positive. Molecular testing of the examined swabs confirmed that 24% of the tested animals were positive. Our sequencing analysis confirmed that the circulating strains of FMDV belonged to FMDV serotype O. The phylogenetic tree based on the FMDV-VP-1 gene revealed high nucleotide identity between the circulating strains and the Bangladesh strain (99%). These strains were distinct (shared 89% nucleotide identity) from the FMDV-O strains used for the preparation of the vaccine administered to the animals in this herd. Moreover, they had 7% nucleotide difference between the FMDV-O strains reported in Saudi Arabian in 2013.

          Conclusion: More in-depth molecular characterization of these FMDV strains is warranted.

          Related collections

          Most cited references40

          • Record: found
          • Abstract: not found
          • Article: not found

          On the Validity of Inferences from Non-random Sample

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found
            Is Open Access

            Understanding the transmission of foot-and-mouth disease virus at different scales

            Foot-and-mouth disease (FMD) is highly infectious, but despite the large quantities of FMD virus released into the environment and the extreme susceptibility of host species to infection, transmission is not always predictable. Whereas virus spread in endemic settings is characterised by frequent direct and indirect animal contacts, incursions into FMD-free countries may be seeded by low-probability events such as fomite or wind-borne aerosol routes. There remains a void between data generated from small-scale experimental studies and our ability to reliably reconstruct transmission routes at different scales between farms, countries and regions. This review outlines recent transmission studies in susceptible host species, and considers new approaches that integrate virus genomics and epidemiological data to recreate and understand the spread of FMD.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Pathogenesis of Primary Foot-and-Mouth Disease Virus Infection in the Nasopharynx of Vaccinated and Non-Vaccinated Cattle

              A time-course pathogenesis study was performed to compare and contrast primary foot-and-mouth disease virus (FMDV) infection following simulated-natural (intra-nasopharyngeal) virus exposure of cattle that were non-vaccinated or vaccinated using a recombinant adenovirus-vectored FMDV vaccine. FMDV genome and infectious virus were detected during the initial phase of infection in both categories of animals with consistent predilection for the nasopharyngeal mucosa. A rapid progression of infection with viremia and widespread dissemination of virus occurred in non-vaccinated animals whilst vaccinated cattle were protected from viremia and clinical FMD. Analysis of micro-anatomic distribution of virus during early infection by lasercapture microdissection localized FMDV RNA to follicle-associated epithelium of the nasopharyngeal mucosa in both groups of animals, with concurrent detection of viral genome in nasopharyngeal MALT follicles in vaccinated cattle only. FMDV structural and non-structural proteins were detected in epithelial cells of the nasopharyngeal mucosa by immunomicroscopy 24 hours after inoculation in both non-vaccinated and vaccinated steers. Co-localization of CD11c+/MHC II+ cells with viral protein occurred early at primary infection sites in vaccinated steers while similar host-virus interactions were observed at later time points in non-vaccinated steers. Additionally, numerous CD8+/CD3- host cells, representing presumptive natural killer cells, were observed in association with foci of primary FMDV infection in the nasopharyngeal mucosa of vaccinated steers but were absent in non-vaccinated steers. Immunomicroscopic evidence of an activated antiviral response at primary infection sites of vaccinated cattle was corroborated by a relative induction of interferon -α, -β, -γ and -λ mRNA in micro-dissected samples of nasopharyngeal mucosa. Although vaccination protected cattle from viremia and clinical FMD, there was subclinical infection of epithelial cells of the nasopharyngeal mucosa that could enable shedding and long-term persistence of infectious virus. Additionally, these data indicate different mechanisms within the immediate host response to infection between non-vaccinated and vaccinated cattle.
                Bookmark

                Author and article information

                Journal
                Vet Q
                Vet Q
                TVEQ
                tveq20
                The Veterinary Quarterly
                Taylor & Francis
                0165-2176
                1875-5941
                2018
                09 January 2019
                : 38
                : 1
                : 88-98
                Affiliations
                [a ]Department of Microbiology and Parasitology, College of Veterinary Medicine, King Faisal University , Al-Hasa, Saudi Arabia;
                [b ]Department of Virology, Faculty of Veterinary Medicine, Kafrelsheikh University , Kafelsheikh, Egypt;
                [c ]Department of Veterinary Public Health, College of Veterinary Medicine, King Faisal University , Al-Hasa, Saudi Arabia;
                [d ]Food Control Department, Faculty of Veterinary Medicine, Zagazig University , Al Sharqia Governorate, Egypt;
                [e ]Department of Pathology, College of Veterinary medicine, King Faisal University , Saudi Arabia;
                [f ]Department of Pathology, College of Veterinary Medicine, Suez Canal University , Ismailia Governorate, Egypt
                Author notes
                CONTACT Maged Gomaa Hemida mhemida@ 123456kfu.edu.sa Department of Microbiology and Parasitology, College of Veterinary Medicine, King Faisal University , Al-Hufuf, Al-Ahsa, Bo Box: 400, Saudi Arabia
                Author information
                http://orcid.org/0000-0002-5986-7237
                Article
                1539568
                10.1080/01652176.2018.1539568
                6831000
                30706772
                5598acd7-d96b-4b52-bcdf-dee2a93dee64
                © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 May 2018
                : 16 October 2018
                : 19 October 2018
                Page count
                Figures: 5, Tables: 1, Pages: 14, Words: 6329
                Funding
                Funded by: King Faisal University for the moral
                Award ID: 170010
                We thank the deanship of scientific research at the King Faisal University for the moral and financial support (Grant No: 170010)
                Categories
                Original Article

                cattle,foot-and-mouth disease,pcr,pathology,serotype o,saudi arabia

                Comments

                Comment on this article