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      Septicaemia of subterranean termites Coptotermes curvignathus caused by disturbance of bacteria isolated from termite gut and its foraging pathways

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          Abstract

          Microbial pathogens continue to attract a great deal of attention to manage the termite population. Every bacterium has its own mode of action and in fact, the mechanisms used by bacteria to attack termites remain elusive at the moment. Hence, the objective of this study was to evaluate the susceptibility of subterranean termites Coptotermes curvignathus to opportunistic pathogens using culturable aerobic bacteria isolated from the termite gut and its foraging pathways. Bacterial suspensions were prepared in concentrations of 10 3, 10 6 and 10 9 colony-forming units (CFU) ml −1 and introduced to the termites via oral-contact and physical contact treatment. The data show that contact method acted slower and gave lower mortality, compared to the oral-contact method. Coptotermes curvignathus were highly susceptible to Serratia marcescens and Pseudomonas aeruginosa. Serratia marcescens showed the highest mortality percentage of 68% and 54% at bacterial concentration of 10 9 CFU ml −1 via oral-contact and contact method, respectively. Serratia marcescens was also defined as the bacteria with the highest ability to induce the high mortality of C. curvignathus with the lowest concentration of bacterial suspension at a given time under laboratory condition. The results of this study indicate that P. aeruginosa and S. marcescens in particular may be attractive candidates worth further examination as a possible biocontrol agent against C. curvignathus in the field and to evaluate environmental and ecological risks of the biocontrol.

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          Common virulence factors for bacterial pathogenicity in plants and animals.

          A Pseudomonas aeruginosa strain (UCBPP-PA14) is infectious both in an Arabidopsis thaliana leaf infiltration model and in a mouse full-thickness skin burn model. UCBPP-PA14 exhibits ecotype specificity for Arabidopsis, causing a range of symptoms from none to severe in four different ecotypes. In the mouse model, UCBPP-PA14 is as lethal as other well-studied P. aeruginosa strains. Mutations in the UCBPP-PA14 toxA, plcS, and gacA genes resulted in a significant reduction in pathogenicity in both hosts, indicating that these genes encode virulence factors required for the full expression of pathogenicity in both plants and animals.
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            Killing of Caenorhabditis elegans by Pseudomonas aeruginosa used to model mammalian bacterial pathogenesis

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              Multiple Toxin-Antitoxin Systems in Mycobacterium tuberculosis

              The hallmark of Mycobacterium tuberculosis is its ability to persist for a long-term in host granulomas, in a non-replicating and drug-tolerant state, and later awaken to cause disease. To date, the cellular factors and the molecular mechanisms that mediate entry into the persistence phase are poorly understood. Remarkably, M. tuberculosis possesses a very high number of toxin-antitoxin (TA) systems in its chromosome, 79 in total, regrouping both well-known (68) and novel (11) families, with some of them being strongly induced in drug-tolerant persisters. In agreement with the capacity of stress-responsive TA systems to generate persisters in other bacteria, it has been proposed that activation of TA systems in M. tuberculosis could contribute to its pathogenesis. Herein, we review the current knowledge on the multiple TA families present in this bacterium, their mechanism, and their potential role in physiology and virulence.
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                Author and article information

                Journal
                R Soc Open Sci
                R Soc Open Sci
                RSOS
                royopensci
                Royal Society Open Science
                The Royal Society
                2054-5703
                August 2020
                26 August 2020
                26 August 2020
                : 7
                : 8
                : 200847
                Affiliations
                [1 ]Institute of Tropical Forestry and Forest Product, Universiti Putra Malaysia , 43400 Serdang, Selangor, Malaysia
                [2 ]Faculty of Forestry and Environment, Universiti Putra Malaysia , 43400 Serdang, Selangor, Malaysia
                Author notes
                Authors for correspondence: Kit Ling Chin e-mail: kitling.chin419@ 123456gmail.com
                Authors for correspondence: Paik San H'ng e-mail: ngpaiksan@ 123456gmail.com
                [†]

                Institute of Tropical Forestry and Forest Products, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.

                Author information
                http://orcid.org/0000-0002-2293-4088
                http://orcid.org/0000-0002-8584-9198
                Article
                rsos200847
                10.1098/rsos.200847
                7481678
                32968530
                57bf7cd9-827f-4681-a506-0773aca685aa
                © 2020 The Authors.

                Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

                History
                : 16 May 2020
                : 30 July 2020
                Funding
                Funded by: Ministry of Higher Education, Malaysia, http://dx.doi.org/10.13039/501100003093;
                Award ID: Fundamental Research Grant Scheme (FRGS) FRGS/1/20
                Award ID: Higher Institution Centre of Excellence (HICoE) wi
                Categories
                1001
                60
                200
                Ecology, Conservation, and Global Change Biology
                Research Article
                Custom metadata
                August, 2020

                coptotermes curvignathus,by oral-contact,by contact,bacterial concentration,biocontrol efficiency

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