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      High-throughput sequencing technologies in the detection of livestock pathogens, diagnosis, and zoonotic surveillance

      review-article
      a , 1 , b , 1 , c , b , d , a , e , f , * , e , g , *
      Computational and Structural Biotechnology Journal
      Research Network of Computational and Structural Biotechnology
      Domestic animals, High-throughput sequencing, Next-generation sequencing, Infectious diseases, Zoonotic pathogens, HTS, High-throughput sequencing, NGS, next-generation sequencing, PCR, polymerase chain reaction, qRT-PCR, quantitative reverse transcription polymerase chain reaction, BLAST, basic local alignment search tool, WG-NGS, whole-genome-NGS, BRD, Bovine respiratory disease, RABV, rabies virus, PGI2, Proteus genomic island 2, APEC, avian pathogenic E. coli, TCR, T-cell receptor, MRSA, Methicillin-resistant Staphylococcus aureus, WGS, whole-genome sequencing, GHSA, Global Health Security Agenda, mNGS, metagenomic next-generation sequencing, COVID-19, coronavirus disease 2019, ACE2, angiotensin-converting enzyme II, ILTV, infectious laryngotracheitis virus

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          Graphical abstract

          Overview of impact of sequencing technologies and its applications in livestock research.

          Abstract

          Increasing globalization, agricultural intensification, urbanization, and climatic changes have resulted in a significant recent increase in emerging infectious zoonotic diseases. Zoonotic diseases are becoming more common, so innovative, effective, and integrative research is required to better understand their transmission, ecological implications, and dynamics at wildlife-human interfaces. High-throughput sequencing (HTS) methodologies have enormous potential for unraveling these contingencies and improving our understanding, but they are only now beginning to be realized in livestock research. This study investigates the current state of use of sequencing technologies in the detection of livestock pathogens such as bovine, dogs ( Canis lupus familiaris), sheep ( Ovis aries), pigs ( Sus scrofa), horses ( Equus caballus), chicken ( Gallus gallus domesticus), and ducks ( Anatidae) as well as how it can improve the monitoring and detection of zoonotic infections. We also described several high-throughput sequencing approaches for improved detection of known, unknown, and emerging infectious agents, resulting in better infectious disease diagnosis, as well as surveillance of zoonotic infectious diseases. In the coming years, the continued advancement of sequencing technologies will improve livestock research and hasten the development of various new genomic and technological studies on farm animals.

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          Most cited references141

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          A pneumonia outbreak associated with a new coronavirus of probable bat origin

          Since the outbreak of severe acute respiratory syndrome (SARS) 18 years ago, a large number of SARS-related coronaviruses (SARSr-CoVs) have been discovered in their natural reservoir host, bats 1–4 . Previous studies have shown that some bat SARSr-CoVs have the potential to infect humans 5–7 . Here we report the identification and characterization of a new coronavirus (2019-nCoV), which caused an epidemic of acute respiratory syndrome in humans in Wuhan, China. The epidemic, which started on 12 December 2019, had caused 2,794 laboratory-confirmed infections including 80 deaths by 26 January 2020. Full-length genome sequences were obtained from five patients at an early stage of the outbreak. The sequences are almost identical and share 79.6% sequence identity to SARS-CoV. Furthermore, we show that 2019-nCoV is 96% identical at the whole-genome level to a bat coronavirus. Pairwise protein sequence analysis of seven conserved non-structural proteins domains show that this virus belongs to the species of SARSr-CoV. In addition, 2019-nCoV virus isolated from the bronchoalveolar lavage fluid of a critically ill patient could be neutralized by sera from several patients. Notably, we confirmed that 2019-nCoV uses the same cell entry receptor—angiotensin converting enzyme II (ACE2)—as SARS-CoV.
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            Coming of age: ten years of next-generation sequencing technologies.

            Since the completion of the human genome project in 2003, extraordinary progress has been made in genome sequencing technologies, which has led to a decreased cost per megabase and an increase in the number and diversity of sequenced genomes. An astonishing complexity of genome architecture has been revealed, bringing these sequencing technologies to even greater advancements. Some approaches maximize the number of bases sequenced in the least amount of time, generating a wealth of data that can be used to understand increasingly complex phenotypes. Alternatively, other approaches now aim to sequence longer contiguous pieces of DNA, which are essential for resolving structurally complex regions. These and other strategies are providing researchers and clinicians a variety of tools to probe genomes in greater depth, leading to an enhanced understanding of how genome sequence variants underlie phenotype and disease.
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              PacBio Sequencing and Its Applications

              Single-molecule, real-time sequencing developed by Pacific BioSciences offers longer read lengths than the second-generation sequencing (SGS) technologies, making it well-suited for unsolved problems in genome, transcriptome, and epigenetics research. The highly-contiguous de novo assemblies using PacBio sequencing can close gaps in current reference assemblies and characterize structural variation (SV) in personal genomes. With longer reads, we can sequence through extended repetitive regions and detect mutations, many of which are associated with diseases. Moreover, PacBio transcriptome sequencing is advantageous for the identification of gene isoforms and facilitates reliable discoveries of novel genes and novel isoforms of annotated genes, due to its ability to sequence full-length transcripts or fragments with significant lengths. Additionally, PacBio’s sequencing technique provides information that is useful for the direct detection of base modifications, such as methylation. In addition to using PacBio sequencing alone, many hybrid sequencing strategies have been developed to make use of more accurate short reads in conjunction with PacBio long reads. In general, hybrid sequencing strategies are more affordable and scalable especially for small-size laboratories than using PacBio Sequencing alone. The advent of PacBio sequencing has made available much information that could not be obtained via SGS alone.
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                Author and article information

                Contributors
                Journal
                Comput Struct Biotechnol J
                Comput Struct Biotechnol J
                Computational and Structural Biotechnology Journal
                Research Network of Computational and Structural Biotechnology
                2001-0370
                26 September 2022
                2022
                26 September 2022
                : 20
                : 5378-5392
                Affiliations
                [a ]Interdisciplinary Graduate Program in Advanced Convergence Technology and Science, Jeju National University, Jeju-si 63243, Republic of Korea
                [b ]Department of Molecular Biology and Genetic Engineering, School of Bioengineering and Biosciences, Lovely Professional University, Punjab, India
                [c ]Section of Surgical Sciences and Epithelial Biology Center, Vanderbilt University Medical Center, Nashville, TN, USA
                [d ]Department of Science and Technology, Ministry of Science and Technology, Govt. of India, Technology Bhavan, New Delhi, India
                [e ]Department of Animal Biotechnology, Faculty of Biotechnology, College of Applied Life Sciences, Jeju National University, Jeju-si 63243, Republic of Korea
                [f ]Bio-Health Materials Core-Facility Center, Jeju National University, Jeju-si 63243, Republic of Korea
                [g ]Department of Biotechnology, School of Bio, Chemical and Processing Engineering (SBCE), Kalasalin-gam Academy of Research and Educational, Krishnankoil 626126, India
                Author notes
                [1]

                S.G.G.D and B.S. contributed equally and Co-First Author.

                Article
                S2001-0370(22)00433-0
                10.1016/j.csbj.2022.09.028
                9526013
                36212529
                06f92b6a-016a-4206-8d96-91457631c382
                © 2022 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 19 March 2022
                : 20 September 2022
                : 21 September 2022
                Categories
                Review

                domestic animals,high-throughput sequencing,next-generation sequencing,infectious diseases,zoonotic pathogens,hts, high-throughput sequencing,ngs, next-generation sequencing,pcr, polymerase chain reaction,qrt-pcr, quantitative reverse transcription polymerase chain reaction,blast, basic local alignment search tool,wg-ngs, whole-genome-ngs,brd, bovine respiratory disease,rabv, rabies virus,pgi2, proteus genomic island 2,apec, avian pathogenic e. coli,tcr, t-cell receptor,mrsa, methicillin-resistant staphylococcus aureus,wgs, whole-genome sequencing,ghsa, global health security agenda,mngs, metagenomic next-generation sequencing,covid-19, coronavirus disease 2019,ace2, angiotensin-converting enzyme ii,iltv, infectious laryngotracheitis virus

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