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      Actinobacillus pleuropneumoniae, surface proteins and virulence: a review

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          Abstract

          Actinobacillus pleuropneumoniae (App) is a globally distributed Gram-negative bacterium that produces porcine pleuropneumonia. This highly contagious disease produces high morbidity and mortality in the swine industry. However, no effective vaccine exists to prevent it. The infection caused by App provokes characteristic lesions, such as edema, inflammation, hemorrhage, and necrosis, that involve different virulence factors. The colonization and invasion of host surfaces involved structures and proteins such as outer membrane vesicles (OMVs), pili, flagella, adhesins, outer membrane proteins (OMPs), also participates proteases, autotransporters, and lipoproteins. The recent findings on surface structures and proteins described in this review highlight them as potential immunogens for vaccine development.

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          Most cited references157

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          Outer-membrane vesicles from Gram-negative bacteria: biogenesis and functions.

          Outer-membrane vesicles (OMVs) are spherical buds of the outer membrane filled with periplasmic content and are commonly produced by Gram-negative bacteria. The production of OMVs allows bacteria to interact with their environment, and OMVs have been found to mediate diverse functions, including promoting pathogenesis, enabling bacterial survival during stress conditions and regulating microbial interactions within bacterial communities. Additionally, because of this functional versatility, researchers have begun to explore OMVs as a platform for bioengineering applications. In this Review, we discuss recent advances in the study of OMVs, focusing on new insights into the mechanisms of biogenesis and the functions of these vesicles.
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            Bacterial adhesion and entry into host cells.

            Successful establishment of infection by bacterial pathogens requires adhesion to host cells, colonization of tissues, and in certain cases, cellular invasion-followed by intracellular multiplication, dissemination to other tissues, or persistence. Bacteria use monomeric adhesins/invasins or highly sophisticated macromolecular machines such as type III secretion systems and retractile type IV pili to establish a complex host/pathogen molecular crosstalk that leads to subversion of cellular functions and establishment of disease.
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              Bacterial Secretion Systems: An Overview.

              Bacterial pathogens utilize a multitude of methods to invade mammalian hosts, damage tissue sites, and thwart the immune system from responding. One essential component of these strategies for many bacterial pathogens is the secretion of proteins across phospholipid membranes. Secreted proteins can play many roles in promoting bacterial virulence, from enhancing attachment to eukaryotic cells, to scavenging resources in an environmental niche, to directly intoxicating target cells and disrupting their functions. Many pathogens use dedicated protein secretion systems to secrete virulence factors from the cytosol of the bacteria into host cells or the host environment. In general, bacterial protein secretion apparatuses can be divided into classes, based on their structures, functions, and specificity. Some systems are conserved in all classes of bacteria and secrete a broad array of substrates, while others are only found in a small number of bacterial species and/or are specific to only one or a few proteins. In this chapter, we review the canonical features of several common bacterial protein secretion systems, as well as their roles in promoting the virulence of bacterial pathogens. Additionally, we address recent findings that indicate that the innate immune system of the host can detect and respond to the presence of protein secretion systems during mammalian infection.
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                Author and article information

                Contributors
                Role: Role:
                URI : https://loop.frontiersin.org/people/95896/overviewRole: Role: Role: Role: Role: Role:
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                Journal
                Front Vet Sci
                Front Vet Sci
                Front. Vet. Sci.
                Frontiers in Veterinary Science
                Frontiers Media S.A.
                2297-1769
                30 November 2023
                2023
                : 10
                : 1276712
                Affiliations
                [1] 1Laboratorio de Biología Celular y Tisular, Departamento de Morfología, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes , Aguascalientes, Mexico
                [2] 2Laboratorio de Estudios Ambientales, Departamento de Fisiología y Farmacología, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes , Aguascalientes, Mexico
                [3] 3Departamento de Ciencias Veterinaria, Centro de Ciencias Agropecuarias, Universidad Autónoma de Aguascalientes , Aguascalientes, Mexico
                Author notes

                Edited by: Jerry William Simecka, University of North Texas Health Science Center, United States

                Reviewed by: Rosa Estela Quiroz Castañeda, Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias (INIFAP), Mexico; Han Sang Yoo, Seoul National University, Republic of Korea

                *Correspondence: Alma L. Guerrero Barrera, alguerre@ 123456correo.uaa.mx ; lilian.guerrero@ 123456edu.uaa.mx

                †ORCID: Francisco J. Avelar Gonzalez, https://orcid.org/0000-0002-0777-9243

                Teodulo Quezada Tristan, https://orcid.org/0000-0002-3793-4582

                Article
                10.3389/fvets.2023.1276712
                10720984
                38098987
                7d678dac-2dea-4d92-ad4e-1fbe32deab8b
                Copyright © 2023 Soto Perezchica, Guerrero Barrera, Avelar Gonzalez, Quezada Tristan and Macias Marin.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 12 August 2023
                : 17 October 2023
                Page count
                Figures: 2, Tables: 5, Equations: 0, References: 157, Pages: 15, Words: 13822
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was financed through the support of the CONACyT scholarship (615420), through the support of PIB19-3 Host-pathogen relationship between bacteria and eukaryotic cells, and Resources of the Doctorate in Biological Sciences of the Autonomous University of Aguascalientes, Mexico.
                Categories
                Veterinary Science
                Review
                Custom metadata
                Veterinary Infectious Diseases

                actinobacillus pleuropneumoniae,bacterial envelope,membrane proteins,proteome,vaccine,biofilm

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