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      Heterotrimeric G-alpha subunits Gpa11 and Gpa12 define a transduction pathway that control spore size and virulence in Mucor circinelloides

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          Abstract

          Mucor circinelloides is one of the causal agents of mucormycosis, an emerging and high mortality rate fungal infection produced by asexual spores (sporangiospores) of fungi that belong to the order Mucorales. M. circinelloides has served as a model genetic system to understand the virulence mechanism of this infection. Although the G-protein signaling cascade plays crucial roles in virulence in many pathogenic fungi, its roles in Mucorales are yet to be elucidated. Previous study found that sporangiospore size and calcineurin are related to the virulence in Mucor, in which larger spores are more virulent in an animal mucormycosis model and loss of a calcineurin A catalytic subunit CnaA results in larger spore production and virulent phenotype. The M. circinelloides genome is known to harbor twelve gpa ( gpa1 to gpa12) encoding G-protein alpha subunits and the transcripts of the gpa11 and gpa12 comprise nearly 72% of all twelve gpa genes transcript in spores. In this study we demonstrated that loss of function of Gpa11 and Gpa12 led to larger spore size associated with reduced activation of the calcineurin pathway. Interestingly, we found lower levels of the cnaA mRNAs in sporangiospores from the Δ gpa12 and double Δ gpa11gpa12 mutant strains compared to wild-type and the Δ cnaA mutant had significantly lower gpa11 and gpa12 mRNA levels compared to wild-type. However, in contrast to the high virulence showed by the large spores of Δ cnaA, the spores from Δ gpa11gpa12 were avirulent and produced lower tissue invasion and cellular damage, suggesting that the gpa11 and gpa12 define a signal pathway with two branches. One of the branches controls spore size through regulation of calcineurin pathway, whereas virulences is controlled by an independent pathway. This virulence-related regulatory pathway could control the expression of genes involved in cellular responses important for virulence, since sporangiospores of Δ gpa11gpa12 were less resistant to oxidative stress and phagocytosis by macrophages than the Δ cnaA and wild-type strains. The characterization of this pathway could contribute to decipher the signals and mechanism used by Mucorales to produce mucormycosis.

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          The epidemiology and clinical manifestations of mucormycosis: a systematic review and meta-analysis of case reports

          The epidemiology of mucormycosis in the era of modern diagnostics is relatively under-explored.
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            Pathogenesis of mucormycosis.

            Mucormycosis is a life-threatening infection that occurs in patients who are immunocompromised because of diabetic ketoacidosis, neutropenia, organ transplantation, and/or increased serum levels of available iron. Because of the increasing prevalence of diabetes mellitus, cancer, and organ transplantation, the number of patients at risk for this deadly infection is increasing. Despite aggressive therapy, which includes disfiguring surgical debridement and frequently adjunctive toxic antifungal therapy, the overall mortality rate is high. New strategies to prevent and treat mucormycosis are urgently needed. Understanding the pathogenesis of mucormycosis and the host response to invading hyphae ultimately will provide targets for novel therapeutic interventions. In this supplement, we review the current knowledge about the virulence traits used by the most common etiologic agent of mucormycosis, Rhizopus oryzae. Because patients with elevated serum levels of available iron are uniquely susceptible to mucormycosis and these infections are highly angioinvasive, emphasis is placed on the ability of the organism to acquire iron from the host and on its interactions with endothelial cells lining blood vessels. Several promising therapeutic strategies in preclinical stages are identified.
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              Regulation, Signaling, and Physiological Functions of G-Proteins.

              Heterotrimeric guanine-nucleotide-binding regulatory proteins (G-proteins) mainly relay the information from G-protein-coupled receptors (GPCRs) on the plasma membrane to the inside of cells to regulate various biochemical functions. Depending on the targeted cell types, tissues, and organs, these signals modulate diverse physiological functions. The basic schemes of heterotrimeric G-proteins have been outlined. In this review, we briefly summarize what is known about the regulation, signaling, and physiological functions of G-proteins. We then focus on a few less explored areas such as the regulation of G-proteins by non-GPCRs and the physiological functions of G-proteins that cannot be easily explained by the known G-protein signaling pathways. There are new signaling pathways and physiological functions for G-proteins to be discovered and further interrogated. With the advancements in structural and computational biological techniques, we are closer to having a better understanding of how G-proteins are regulated and of the specificity of G-protein interactions with their regulators.
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                Author and article information

                Contributors
                Role: Data curationRole: Investigation
                Role: Data curationRole: InvestigationRole: Methodology
                Role: ConceptualizationRole: Investigation
                Role: InvestigationRole: Methodology
                Role: Data curationRole: Methodology
                Role: Data curationRole: Methodology
                Role: Funding acquisitionRole: Methodology
                Role: Data curationRole: Formal analysisRole: Methodology
                Role: ConceptualizationRole: Formal analysisRole: Methodology
                Role: Data curationRole: Formal analysisRole: InvestigationRole: MethodologyRole: ResourcesRole: Writing – review & editing
                Role: Formal analysisRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: ResourcesRole: Writing – review & editing
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: Funding acquisitionRole: InvestigationRole: MethodologyRole: Project administrationRole: ResourcesRole: SupervisionRole: ValidationRole: Writing – original draftRole: Writing – review & editing
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                30 December 2019
                2019
                : 14
                : 12
                : e0226682
                Affiliations
                [1 ] Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo (UMSNH), Morelia, Michoacán, México
                [2 ] Departamento de Biología Molecular, Laboratorio Estatal de Salud Pública del Estado de Michoacán, Morelia, Michoacán, México
                [3 ] Departamento de Genética y Microbiología, Facultad de Biología, Universidad de Murcia, Murcia, España
                [4 ] Facultad de Medicina Veterinaria y Zootecnia, Universidad Michoacana de San Nicolás Hidalgo, Morelia, Michoacán, Mexico
                [5 ] Facultad de Ciencias de la Salud, Universidad Anáhuac, Naucalpan de Juarez, Estado de México, México
                [6 ] Facultad de Químico Farmacobiología, Universidad Michoacana de San Nicolás de Hidalgo, Morelia, Michoacan, México
                [7 ] Department of Biology, South Texas Center of Emerging Infectious Diseases (STCEID), University of Texas at San Antonio, San Antonio, Texas, United States of America
                Soonchunhyang University, REPUBLIC OF KOREA
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Author information
                http://orcid.org/0000-0003-1384-3608
                http://orcid.org/0000-0002-1117-9136
                http://orcid.org/0000-0002-8337-5830
                http://orcid.org/0000-0002-0125-346X
                http://orcid.org/0000-0001-7605-1726
                http://orcid.org/0000-0003-2838-7211
                Article
                PONE-D-19-09579
                10.1371/journal.pone.0226682
                6936849
                31887194
                848b8a65-6581-4624-9b18-f708a8a98b59
                © 2019 Patiño-Medina et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 3 April 2019
                : 3 December 2019
                Page count
                Figures: 11, Tables: 0, Pages: 26
                Funding
                V M-C, MI R-D Coordinación de la Investigación Científica, Universidad Michoacana de San Nicolás de Hidalgo, México (2.6, 2.35). https://www.cic.umich.mx V M-C, MI R-D, J C-G Consejo Nacional de Ciencia y Tecnología, México (CONACYT; 181747, 167071, and 256119). https://www.conacyt.gob.mx V G Fundación Séneca-Agencia de Ciencia y Tecnología de la Región de Murcia, Spain (19339/PI/14). https://www.fseneca.es The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Mycology
                Fungal Reproduction
                Fungal Spores
                Biology and Life Sciences
                Genetics
                Mutation
                Mutant Strains
                Biology and Life Sciences
                Mycology
                Fungal Reproduction
                Fungal Spore Germination
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Artificial Gene Amplification and Extension
                Polymerase Chain Reaction
                Research and Analysis Methods
                Molecular Biology Techniques
                Artificial Gene Amplification and Extension
                Polymerase Chain Reaction
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                Oligonucleotides
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                Medicine and Health Sciences
                Immunology
                Immune Cells
                White Blood Cells
                Macrophages
                Biology and Life Sciences
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