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      Current treatment options for leptospirosis: a mini-review

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          Abstract

          Leptospirosis, one of the most common global zoonotic infections, significantly impacts global human health, infecting more than a million people and causing approximately 60,000 deaths annually. This mini-review explores effective treatment strategies for leptospirosis, considering its epidemiology, clinical manifestations, and current therapeutic approaches. Emphasis is placed on antibiotic therapy, including recommendations for mild and severe cases, as well as the role of probiotics in modulating the gut microbiota. Furthermore, novel treatment options, such as bacteriophages and newly synthesized/natural compounds, are discussed, and the findings are expected to provide insights into promising approaches for combating leptospirosis.

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          Most cited references119

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          Role of the microbiota in immunity and inflammation.

          The microbiota plays a fundamental role on the induction, training, and function of the host immune system. In return, the immune system has largely evolved as a means to maintain the symbiotic relationship of the host with these highly diverse and evolving microbes. When operating optimally, this immune system-microbiota alliance allows the induction of protective responses to pathogens and the maintenance of regulatory pathways involved in the maintenance of tolerance to innocuous antigens. However, in high-income countries, overuse of antibiotics, changes in diet, and elimination of constitutive partners, such as nematodes, may have selected for a microbiota that lack the resilience and diversity required to establish balanced immune responses. This phenomenon is proposed to account for some of the dramatic rise in autoimmune and inflammatory disorders in parts of the world where our symbiotic relationship with the microbiota has been the most affected. Copyright © 2014 Elsevier Inc. All rights reserved.
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            The microbiota in adaptive immune homeostasis and disease.

            In the mucosa, the immune system's T cells and B cells have position-specific phenotypes and functions that are influenced by the microbiota. These cells play pivotal parts in the maintenance of immune homeostasis by suppressing responses to harmless antigens and by enforcing the integrity of the barrier functions of the gut mucosa. Imbalances in the gut microbiota, known as dysbiosis, can trigger several immune disorders through the activity of T cells that are both near to and distant from the site of their induction. Elucidation of the mechanisms that distinguish between homeostatic and pathogenic microbiota-host interactions could identify therapeutic targets for preventing or modulating inflammatory diseases and for boosting the efficacy of cancer immunotherapy.
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              The gut–liver axis and the intersection with the microbiome

              In the past decade, an exciting realization has been that diverse liver diseases, ranging from non-alcoholic steatohepatitis, alcoholic steatohepatitis, and cirrhosis, to hepatocellular carcinoma, are not unrelated but fall along a spectrum. Recent work on the biology of the gut-liver communication axis has assisted in understanding the basic biology of both alcoholic and nonalcoholic fatty liver disease. Of immense importance is the massive advancement in understanding of the role of the microbiome, driven by high-throughput DNA sequencing and improved computational techniques that allow the complexity of the microbiome to be interrogated, together with improved experimental designs. Here, we review the gut-liver communications of these various forms of liver disease, explore the molecular, genetic and microbiome relationships, discuss prospects for exploiting the microbiome to determine the stage of liver disease, and to predict the effects of pharmaceutical, dietary, and other interventions at a population and individual level. We conclude that although much remains to be done in understanding the relationship between the microbiome and liver disease, rapid progress towards clinical applications is being made, especially in study designs that complement human intervention studies with mechanistic work in mice that have been humanized in multiple respects, including the genetic, immunological and microbiome characteristics of individual patients. These “avatar mice” may be especially useful for guiding new microbiome-based or microbiome-informed therapies.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                25 April 2024
                2024
                : 15
                : 1403765
                Affiliations
                [1] 1Department of Biochemistry and Pharmacology, Uzhhorod National University , Uzhhorod, Ukraine
                [2] 2Department of Microbiology, Virology, and Immunology, I. Horbachevsky Ternopil National Medical University , Ternopil, Ukraine
                [3] 3Department of Microbiology, Shahr-e-Qods Branch, Islamic Azad University , Tehran, Iran
                [4] 4Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen , Bergen, Norway
                Author notes

                Edited by: Axel Cloeckaert, Institut National de recherche pour l’agriculture, l’alimentation et l’environnement (INRAE), France

                Reviewed by: Fernando P. Monroy, Northern Arizona University, United States

                Mario D'incau, Experimental Zooprophylactic Institute of Lombardy and Emilia Romagna (IZSLER), Italy

                *Correspondence: Pavlo Petakh, pavlo.petakh@ 123456uzhnu.edu.ua
                Valentyn Oksenych oksenych@ 123456gmail.com
                Article
                10.3389/fmicb.2024.1403765
                11081000
                38725681
                f9b1c636-682c-458e-9bc7-3028a8d50982
                Copyright © 2024 Petakh, Behzadi, Oksenych and Kamyshnyi.

                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
                : 19 March 2024
                : 15 April 2024
                Page count
                Figures: 1, Tables: 0, Equations: 0, References: 120, Pages: 9, Words: 8550
                Funding
                The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
                Categories
                Microbiology
                Mini Review
                Custom metadata
                Infectious Agents and Disease

                Microbiology & Virology
                leptospira interrogans,antibiotic,corticosteroid,probiotic,leptospirosis
                Microbiology & Virology
                leptospira interrogans, antibiotic, corticosteroid, probiotic, leptospirosis

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