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Artykuły w czasopismach na temat „Commensalism”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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1

Georgescu, Paul, Daniel Maxin, and Hong Zhang. "Global stability results for models of commensalism." International Journal of Biomathematics 10, no. 03 (2017): 1750037. http://dx.doi.org/10.1142/s1793524517500371.

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We analyze the global stability of the coexisting equilibria for several models of commensalism, first by devising a procedure to modify several Lyapunov functionals which were introduced earlier for corresponding models of mutualism, further confirming their usefulness. It is seen that commensalism promotes global stability, in connection with higher-order self-limiting terms which prevent unboundedness. We then use the theory of asymptotically autonomous systems to prove global stability results for models of commensalism which are subject to Allee effects, finding that commensalisms of appr

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2

Mathis, Kaitlyn A., and Judith L. Bronstein. "Our Current Understanding of Commensalism." Annual Review of Ecology, Evolution, and Systematics 51, no. 1 (2020): 167–89. http://dx.doi.org/10.1146/annurev-ecolsys-011720-040844.

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Commensalisms, interactions between two species in which one species benefits and the other experiences no net effect, are frequently mentioned in the ecological literature but are surprisingly little studied. Here we review and synthesize our limited understanding of commensalism. We then argue that commensalism is not a single type of interaction; rather, it is a suite of phenomena associated with distinct ecological processes and evolutionary consequences. For each form of commensalism we define, we present evidence for how, where, and why it occurs, including when it is evolutionarily pers

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3

Hulme-Beaman, A., K. Dobney, T. Cucchi, and JB Searle. "An ecological and evolutionary framework for commensalism in anthropogenic environments." Trends in Ecology & Evolution 31 (June 7, 2016): 633–45. https://doi.org/10.1016/j.tree.2016.05.001.

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Commensalism within anthropogenic environments has not been extensively discussed, despite its impact on humans, and there is no formal framework for assessing this ecological relationship in its varied forms. Here, we examine commensalism in anthropogenic environments in detail, considering both ecological and evolutionary drivers. The many assumptions about commensalism and the nature of anthropogenic environments are discussed and we highlight dependency as a key attribute of anthropogenic commensals (anthrodependent taxa). We primarily focus on mammalian species in the anthropogenic-commen

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4

Balaji, Vignesh Kanna, Latha Ragunathan, Kavitha Kannaiyan, and Jeyakumari Duraipandian. "The role of Malassezia species on Human skin: Commensals and Pathogens." Research Journal of Biotechnology 18, no. 9 (2023): 271–77. http://dx.doi.org/10.25303/1809rjbt2710277.

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Malassezia spp are recognized as skin commensals that may be pathogenic under certain conditions. For many years, it was known as commensals but recently it has been identified causing many superficial skin infections and fungemia. There are many hypotheses regarding the pathogenesis of Malassezia infections. As there is limited data on physiology and pathogenesis of Malassezia, therefore, in recent years new tools has been evolved for Malassezia culture, detection and genetic manipulation which have revealed the ubiquity of Malassezia on skin. As Malassezia cannot synthesize fatty acid, it se

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5

Tobin Kåhrström, Christina. "Converting to commensalism." Nature Reviews Microbiology 11, no. 9 (2013): 597. http://dx.doi.org/10.1038/nrmicro3101.

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6

Romo, Jesus A., and Carol A. Kumamoto. "On Commensalism of Candida." Journal of Fungi 6, no. 1 (2020): 16. http://dx.doi.org/10.3390/jof6010016.

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Candida species are both opportunistic fungal pathogens and common members of the human mycobiome. Over the years, the main focus of the fungal field has been on understanding the pathogenic potential and disease manifestation of these organisms. Therefore, understanding of their commensal lifestyle, interactions with host epithelial barriers, and initial transition into pathogenesis is less developed. In this review, we will describe the current knowledge on the commensal lifestyle of these fungi, how they are able to adhere to and colonize host epithelial surfaces, compete with other members

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7

Blaser, Martin J., and Fred T. Valentine. "Viral Commensalism in Humans?" Journal of Infectious Diseases 198, no. 1 (2008): 1–3. http://dx.doi.org/10.1086/588705.

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8

May, A. "WHY WERE REEFS AND STROMATOPOROIDS SO RARE IN THE LOWER DEVONIAN?" Sciences of Europe, no. 104 (November 7, 2022): 24–32. https://doi.org/10.5281/zenodo.7298618.

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In the middle Lower Devonian, the Pragian, reefs were very rare worldwide and stromatoporoids were rare and little diverse. As an explanation for this phenomenon, it is not sufficient that the global sea level had its low for the Devonian period during the Pragian and Lower Emsian. Therefore, three stromatoporoid-bearing reefs from the Pragian of Western and Central Europe were studied: Koněprusy in the Czech Republic, Seewarte in Austria and Zújar in Southern Spain. The following possible causes for the extreme rarity of reefs in the Pragian emerged: 1) Conspicuously high or low water

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9

Damle, SG. "Commensalism the new scientific revolution?" Contemporary Clinical Dentistry 9, no. 5 (2018): 1. http://dx.doi.org/10.4103/ccd.ccd_403_18.

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10

WATANABE, Takuya. "Commensalism of Wildflowers with Weeds." Journal of the Japanese Society of Revegetation Technology 16, no. 3 (1990): 71–74. http://dx.doi.org/10.7211/jjsrt.16.3_71.

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11

Variyam, Easwaran P. "Commensalism of pathogenic Entamoeba histolytica." Gastroenterology 108, no. 4 (1995): A935. http://dx.doi.org/10.1016/0016-5085(95)28046-4.

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12

Macholán, Miloš, Kristina Daniszová, and Zuzana Hiadlovská. "The Expansion of House Mouse Major Urinary Protein Genes Likely Did Not Facilitate Commensalism with Humans." Genes 14, no. 11 (2023): 2090. http://dx.doi.org/10.3390/genes14112090.

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Mouse wild-derived strains (WDSs) combine the advantages of classical laboratory stocks and wild animals, and thus appear to be promising tools for diverse biomedical and evolutionary studies. We employed 18 WDSs representing three non-synanthropic species (Mus spretus, Mus spicilegus, and M. macedonicus) and three house mouse subspecies (Mus musculus musculus, M. m. domesticus, M. m. castaneus), which are all important human commensals to explore whether the number of major urinary protein (MUP) genes and their final protein levels in urine are correlated with the level of commensalism. Contr

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13

Jawad, Shireen. "Study the Dynamics of Commensalism Interaction with Michaels-Menten Type Prey Harvesting." Al-Nahrain Journal of Science 25, no. 1 (2022): 45–50. http://dx.doi.org/10.22401/anjs.25.1.08.

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This paper suggests and analyses a model consisting of two commensal populations with Michaelis-Menten type of harvesting for the first population. The first harvested commensal species draws strength from the second hosted species. The overall dynamics are provided to achieve the coexistence, stability and persistence of the equilibrium points for the proposed system. The local bifurcation near the positive equilibrium point is attained. Moreover, numerical simulation using MATLAB is investigated to the impact of the commensalism interaction on the behavior of the planned model. The analysis

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14

Nayak, Sangeeta, Nishmitha D. Shetty, and Deepa G. Kamath. "Commensalism of Fusobacterium nucleatum - The dilemma." Journal of Indian Society of Periodontology 28, no. 4 (2024): 427–30. https://doi.org/10.4103/jisp.jisp_286_23.

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Fusobacterium nucleatum is a Gram-negative, anaerobic bacterium that serves as a periodontal pathogen and plays a key role in linking Gram-positive and Gram-negative bacteria within the periodontal biofilm. It was shown that Fusobacterium produces significant amounts of butyric acid, which is a great source of energy for anti-inflammatory cells. On the other hand, it is associated with the destruction of periodontal structures. This bacterium can enter the blood circulation as a result of periodontal infection. It could cause numerous conditions such as halitosis, dental pulp infection, oral c

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15

Gu, Zi-Qi, Kuo-Yao Tseng, and Yu-Huan Tsai. "Candida gut commensalism and inflammatory disease." Medicine in Microecology 3 (March 2020): 100008. http://dx.doi.org/10.1016/j.medmic.2020.100008.

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16

Gow, Neil A. R. "A developmental program for Candida commensalism." Nature Genetics 45, no. 9 (2013): 967–68. http://dx.doi.org/10.1038/ng.2737.

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17

Bolton, Madeleine. "Clever commensalism in a harsh environment." Frontiers in Ecology and the Environment 20, no. 10 (2022): 580. http://dx.doi.org/10.1002/fee.2579.

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18

Li, Jingchun, Diarmaid Ó Foighil, and Ellen E. Strong. "Commensal associations and benthic habitats shape macroevolution of the bivalve clade Galeommatoidea." Proceedings of the Royal Society B: Biological Sciences 283, no. 1834 (2016): 20161006. http://dx.doi.org/10.1098/rspb.2016.1006.

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The great diversity of marine life has been shaped by the interplay between abiotic and biotic factors. Among different biotic interactions, symbiosis is an important yet less studied phenomenon. Here, we tested how symbiotic associations affected marine diversification, using the bivalve superfamily Galeommatoidea as a study system. This superfamily contains large numbers of obligate commensal as well as free-living species and is therefore amenable to comparative approaches. We constructed a global molecular phylogeny of Galeommatoidea and compared macroevolutionary patterns between free-liv

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19

Zhao, Liang, Bin Qin, and Xianbo Sun. "Dynamic Behavior of a Commensalism Model with Nonmonotonic Functional Response and Density-Dependent Birth Rates." Complexity 2018 (December 2, 2018): 1–6. http://dx.doi.org/10.1155/2018/9862584.

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In this paper, we propose and analyze a commensalism model with nonmonotonic functional response and density-dependent birth rates. The model can have at most four nonnegative equilibria. By applying the differential inequality theory, we show that each equilibrium can be globally attractive under suitable conditions. However, commensalism can be established only when resources for both species are large enough.

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20

Zhao, Kaihong. "Global asymptotic stability for a classical controlled nonlinear periodic commensalism AG-ecosystem with distributed lags on time scales." Filomat 37, no. 29 (2023): 9899–911. http://dx.doi.org/10.2298/fil2329899z.

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Commensalism is a common phenomenon in nature. The Ayala-Gilpin (AG) dynamical system model is commonly used to describe the nonlinear interactions between species in ecosystems. Combining commensalism with AG-system models, the manuscript emphasizes on a classical controlled nonlinear periodic commensalism AG-ecosystem with distributed lags on time scales. In our model, the discrete and continuous cases are unified and generalized in the sense of time scale. Firstly, it is proved that a class of auxiliary functions have only two zeros in the real number field. Then, with the aid of these auxi

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21

Prasad, B. Hari, and N. Ch Pattabhi Ramacharyulu. "Discrete Model of Commensalism Between Two Species." International Journal of Modern Education and Computer Science 4, no. 8 (2012): 40–46. http://dx.doi.org/10.5815/ijmecs.2012.08.06.

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22

Wyncoll, Greg, and Daniel Tangri. "The Origins of Commensalism and Human Sedentism." Paléorient 17, no. 2 (1991): 157–59. http://dx.doi.org/10.3406/paleo.1991.5093.

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23

Nussbaum, J. C., and R. M. Locksley. "Infectious (Non)tolerance--Frustrated Commensalism Gone Awry?" Cold Spring Harbor Perspectives in Biology 4, no. 5 (2012): a007328. http://dx.doi.org/10.1101/cshperspect.a007328.

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24

Prieto, Daniel, Inês Correia, Jesús Pla, and Elvira Román. "Adaptation ofCandida albicansto commensalism in the gut." Future Microbiology 11, no. 4 (2016): 567–83. http://dx.doi.org/10.2217/fmb.16.1.

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25

DE WERT, LEONI, KEVIN MAHON, and GRAEME D. RUXTON. "Protection by association: evidence for aposematic commensalism." Biological Journal of the Linnean Society 106, no. 1 (2012): 81–89. http://dx.doi.org/10.1111/j.1095-8312.2012.01855.x.

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26

Iliev, Iliyan D., and David M. Underhill. "Striking a balance: fungal commensalism versus pathogenesis." Current Opinion in Microbiology 16, no. 3 (2013): 366–73. http://dx.doi.org/10.1016/j.mib.2013.05.004.

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27

Southwick, Charles H., and M. Farooq Siddiqi. "Primate commensalism : the rhesus monkey in India." Revue d'Écologie (La Terre et La Vie) 49, no. 3 (1994): 223–31. http://dx.doi.org/10.3406/revec.1994.2473.

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28

Joshi, Manish, and Julien Royet. "Uridine Catabolism Breaks the Bonds of Commensalism." Cell Host & Microbe 27, no. 3 (2020): 312–14. http://dx.doi.org/10.1016/j.chom.2020.02.008.

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29

Iliev, Iliyan D., and David M. Underhill. "Striking a balance: fungal commensalism versus pathogenesis." Current Opinion in Microbiology 16, no. 3 (2013): 366–73. https://doi.org/10.5281/zenodo.13523440.

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30

Iliev, Iliyan D., and David M. Underhill. "Striking a balance: fungal commensalism versus pathogenesis." Current Opinion in Microbiology 16, no. 3 (2013): 366–73. https://doi.org/10.5281/zenodo.13523440.

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31

Iliev, Iliyan D., and David M. Underhill. "Striking a balance: fungal commensalism versus pathogenesis." Current Opinion in Microbiology 16, no. 3 (2013): 366–73. https://doi.org/10.5281/zenodo.13523440.

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32

Iliev, Iliyan D., and David M. Underhill. "Striking a balance: fungal commensalism versus pathogenesis." Current Opinion in Microbiology 16, no. 3 (2013): 366–73. https://doi.org/10.5281/zenodo.13523440.

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33

Jakobsen, Louise M. A., Maria X. Maldonado-Gómez, Ulrik K. Sundekilde, Henrik J. Andersen, Dennis S. Nielsen, and Hanne C. Bertram. "Metabolic Effects of Bovine Milk Oligosaccharides on Selected Commensals of the Infant Microbiome—Commensalism and Postbiotic Effects." Metabolites 10, no. 4 (2020): 167. http://dx.doi.org/10.3390/metabo10040167.

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Oligosaccharides from human or bovine milk selectively stimulate growth or metabolism of bacteria associated with the lower gastrointestinal tract of infants. Results from complex infant-type co-cultures point toward a possible synergistic effect of combining bovine milk oligosaccharides (BMO) and lactose (LAC) on enhancing the metabolism of Bifidobacterium longum subsp. longum and inhibition of Clostridium perfringens. We examine the interaction between B. longum subsp. longum and the commensal Parabacteroides distasonis, by culturing them in mono- and co-culture with different carbohydrates

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34

Telesford, Kiel, Javier Ochoa-Repáraz, and Lloyd H. Kasper. "Gut Commensalism, Cytokines, and Central Nervous System Demyelination." Journal of Interferon & Cytokine Research 34, no. 8 (2014): 605–14. http://dx.doi.org/10.1089/jir.2013.0134.

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35

Hayashi, T. "MICROBIOLOGY: Breaking the Barrier Between Commensalism and Pathogenicity." Science 313, no. 5788 (2006): 772–73. http://dx.doi.org/10.1126/science.1131752.

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36

ZAPALSKI, MIKOŁAJ K. "PARASITISM VERSUS COMMENSALISM: THE CASE OF TABULATE ENDOBIONTS." Palaeontology 50, no. 6 (2007): 1375–80. http://dx.doi.org/10.1111/j.1475-4983.2007.00716.x.

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37

Roper, Caroline, Claudia Castro, and Brian Ingel. "Xylella fastidiosa: bacterial parasitism with hallmarks of commensalism." Current Opinion in Plant Biology 50 (August 2019): 140–47. http://dx.doi.org/10.1016/j.pbi.2019.05.005.

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38

Xue, Yalong, Xiangdong Xie, Fengde Chen, and Rongyu Han. "Almost Periodic Solution of a Discrete Commensalism System." Discrete Dynamics in Nature and Society 2015 (2015): 1–11. http://dx.doi.org/10.1155/2015/295483.

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A nonautonomous discrete two-species Lotka-Volterra commensalism system with delays is considered in this paper. Based on the discrete comparison theorem, the permanence of the system is obtained. Then, by constructing a new discrete Lyapunov functional, a set of sufficient conditions which guarantee the system global attractivity are obtained. If the coefficients are almost periodic, there exists an almost periodic solution and the almost periodic solution is globally attractive.

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39

Reddy, J. Goverdhan, and Sita B. Rambabu. "A Mathematical Study of Two Species Commensalism Model." Research Journal of Science and Technology 9, no. 3 (2017): 385. http://dx.doi.org/10.5958/2349-2988.2017.00067.5.

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40

TOKESHI, MUTSUNORI. "On the evolution of commensalism in the Chironomidae." Freshwater Biology 29, no. 3 (1993): 481–89. http://dx.doi.org/10.1111/j.1365-2427.1993.tb00782.x.

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41

Sanders, Dirk, and F. J. Frank van Veen. "Indirect commensalism promotes persistence of secondary consumer species." Biology Letters 8, no. 6 (2012): 960–63. http://dx.doi.org/10.1098/rsbl.2012.0572.

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Local species extinctions may lead to, often unexpected, secondary extinctions. To predict these, we need to understand how indirect effects, within a network of interacting species, affect the ability of species to persist. It has been hypothesized that the persistence of some predators depends on other predator species that suppress competitively dominant prey to low levels, allowing a greater diversity of prey species, and their predators, to coexist. We show that, in experimental insect communities, the absence of one parasitoid wasp species does indeed lead to the extinction of another th

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42

Furness, Peter. "Coroners and Medical Examiners: Mutualism, Commensalism or Parasitism?" Medico-Legal Journal 80, no. 3 (2012): 86–101. http://dx.doi.org/10.1258/mlj.2012.012011.

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Han, Geongoo, Rebecca Yunker, Mohammad Hasan, et al. "Host and microbe adaptation underlying true fungal commensalism." Journal of Immunology 210, no. 1_Supplement (2023): 81.11. http://dx.doi.org/10.4049/jimmunol.210.supp.81.11.

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Abstract Fungi are found ubiquitously in the mammalian gut however the role of commensal fungi in the host is poorly understood. Laboratory mice are used to model host-fungi interactions however due to ultra-clean housing they do not harbor fungi. The human commensal fungus Candida albicans is widely studied to dissect host-commensal fungi interactions however prior dysbiosis of commensal bacteria is required to colonize laboratory mice. Insights from such forced host-fungal interactions are unsuitable for extrapolating mechanisms underlying fungal commensalism and its breakdown. To discover t

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44

Romo, Jesús A., and Jose L. Lopez-Ribot. "Candidalysin: An unlikely aide for fungal gut commensalism." Cell Host & Microbe 32, no. 5 (2024): 625–26. http://dx.doi.org/10.1016/j.chom.2024.04.010.

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45

Urrialde, Verónica, Daniel Prieto, Susana Hidalgo-Vico, Elvira Román, Jesús Pla, and Rebeca Alonso-Monge. "Deletion of the SKO1 Gene in a hog1 Mutant Reverts Virulence in Candida albicans." Journal of Fungi 5, no. 4 (2019): 107. http://dx.doi.org/10.3390/jof5040107.

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Candida albicans displays the ability to adapt to a wide variety of environmental conditions, triggering signaling pathways and transcriptional regulation. Sko1 is a transcription factor that was previously involved in early hypoxic response, cell wall remodeling, and stress response. In the present work, the role of sko1 mutant in in vivo and ex vivo studies was explored. The sko1 mutant behaved as its parental wild type strain regarding the ability to colonize murine intestinal tract, ex vivo adhesion to murine gut epithelium, or systemic virulence. These observations suggest that Sko1 is ex

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46

Osuna, Osvaldo, and Geiser Villavicencio-Pulido. "A seasonal commensalism model with a weak Allee effect to describe climate-mediated shifts." Selecciones Matemáticas 11, no. 02 (2024): 212–21. https://doi.org/10.17268/sel.mat.2024.02.01.

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Climate change is affecting the life cycle of tight interacting species. Commonly, the seasonal population dynamics of species is analyzed through models with periodic rates; however, assuming periodicity in seasonal phenomena which depend on environmental drivers is very restrictive. In this work, we analyze seasonal commensalism between two species in which the per capita growth rate of each species is affected by a weak Allee effect and the demographic and ecological rates are assumed almost periodic. To do this, we construct and analyze an almost periodic model to describe commensalism usi

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47

Cornett, James W. "Apparent Commensalism of a Red-tailed Hawk and Badger." Western Birds 52, no. 1 (2021): 80–81. http://dx.doi.org/10.21199/wb52.1.7.

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48

Heard, Stephen B. "Pitcher-Plant Midges and Mosquitoes: A Processing Chain Commensalism." Ecology 75, no. 6 (1994): 1647–60. http://dx.doi.org/10.2307/1939625.

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49

Wang, Yuanyuan, Jia Zhou, Yun Zou, et al. "Fungal commensalism modulated by a dual-action phosphate transceptor." Cell Reports 38, no. 4 (2022): 110293. http://dx.doi.org/10.1016/j.celrep.2021.110293.

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Kreth, J., R. A. Giacaman, R. Raghavan, and J. Merritt. "The road less traveled - defining molecular commensalism withStreptococcus sanguinis." Molecular Oral Microbiology 32, no. 3 (2016): 181–96. http://dx.doi.org/10.1111/omi.12170.

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