Antagonistic Effect of Bacteria Isolated from the Digestive Tract of <i>Lutzomyia evansi</i> against Promastigotes of <i>Leishmania infantum</i>, Antimicrobial Activities and Susceptibility to Antibiotics — Oak Academic Publishing
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Antagonistic Effect of Bacteria Isolated from the Digestive Tract of <i>Lutzomyia evansi</i> against Promastigotes of <i>Leishmania infantum</i>, Antimicrobial Activities and Susceptibility to Antibiotics
Microbiodiversity and Bioprospection Research Group, Cellular and Molecular Biology Laboratory, National University of Colombia, Medellin, Colombia
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Microbiodiversity and Bioprospection Research Group, Cellular and Molecular Biology Laboratory, National University of Colombia, Medellin, Colombia
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Microbiodiversity and Bioprospection Research Group, Cellular and Molecular Biology Laboratory, National University of Colombia, Medellin, Colombia
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PECET-Medical Research Institute, University of Antioquia, Medellin, Colombia
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Molecular Systematics Group, National University of Colombia, Medellin, Colombia
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PECET-Medical Research Institute, University of Antioquia, Medellin, Colombia
1 Microbiodiversity and Bioprospection Research Group, Cellular and Molecular Biology Laboratory, National University of Colombia, Medellin, Colombia
2 Microbiodiversity and Bioprospection Research Group, Cellular and Molecular Biology Laboratory, National University of Colombia, Medellin, Colombia
3 Microbiodiversity and Bioprospection Research Group, Cellular and Molecular Biology Laboratory, National University of Colombia, Medellin, Colombia
4 PECET-Medical Research Institute, University of Antioquia, Medellin, Colombia
5 Molecular Systematics Group, National University of Colombia, Medellin, Colombia
6 PECET-Medical Research Institute, University of Antioquia, Medellin, Colombia
Lutzomyia evansi is a phlebotomine insect endemic to Colombia’s Caribbean coast and is considered the main vector of visceral and cutaneous leishmaniasis in the region. Specific studies of the direct effects generated by bacteria in the digestive tract of the insect vectors, under Leishmania infantum using in vitro models, represent a novel alternative as a control strategy for the transmission of leishmaniasis and also provide the opportunity to detect natural products or antimicrobial peptides with different biological activities. In this study, we evaluate the leishmanicidal and antimicrobial activities of Pantoea ananatis, Ochrobactrum anthropi and Enterobacter cloacae , isolated from the digestive tract of Lutzomyia evansi and the susceptibility of these bacteria to commonly used antibiotics. The antagonistic effect of Pantoea ananatis , Ochrobactrum anthropi and Enterobacter cloacae was evaluated against six species of human pathogenic bacteria and against stationary (Metacyclic-like) and exponential promastigotes (Procyclic-like) of Leishmania infantum (BCN-GFP strain) by co-culture assays for 24 hours. The activity of the bacterial isolates on Leishmania infantum promastigotes was quantified by flow cytometry. The susceptibility of the bacterial strains to clinically used antibiotics was analyzed by antibiogram. The highest percentage of inhibition was observed against exponential promastigotes with bacterial concentrations of 10 8 CFU/ml of Enterobacter cloacae (77.29% ± 0.6%) and Pantoea ananatis (70.17% ± 1.1%). The extracts produced by three bacterial isolates showed similar biological activity (13 mm - 22 mm inhibition halos) against all tested bacteria; however, significant differences were observed with respect to gram-positive bacteria (P < 0.003557). The most active antibacterial activity was displayed against the pathogenic bacteria Bacillus cereus . Ochrobactrum anthropi was the isolate with the highest number of antibiotic resistance patterns while Pantoea ananatis and Enterobacter cloacae showed greater susceptibility to the evaluated antibiotics. The growth inhibitory activity of exponential Leishmania infantum promastigotes shown by extracts of Enterobacter cloacae and Pantoea ananantis suggests that the presence of these bacteria in the vector intestine may affect the parasite development to metacyclic stages, infective to human hosts. This in turn confers said bacteria, a potential in controlling the transmission of Leishmania spp. that deserves to be studied in depth.
Alvar, J., Velez, I., Bern, C., et al. (2012) Leishmaniasis Worldwide and Global Estimates of Its Incidence. PLoS ONE, 7, e35671. http://dx.doi.org/10.1371/journal.pone.0035671
Amora, S., Bevilaqua, C., Feijo, F., Alves, N. and Maciel, M. (2009) Control de Phlebotomine (Diptera: Psychodidae) Leishmaniasis Vectors. Neotropical Entomology, 38, 303-310. http://dx.doi.org/10.1590/S1519-566X2009000300001
Vivero, R., Torres-Gutierrez, C., Bejarano, E., Cadena, H., Estrada, L., Florez, F., et al. (2015) Study on Natural Breeding Sites of Sand Flies (Diptera: Phlebotominae) in Areas of Leishmania Transmission in Colombia. Parasit and Vectors, 8, 116. http://dx.doi.org/10.1186/s13071-015-0711-y
Freitas-Junior, L., Chatelain, L., Andrade, H. and Siqueira-Neto, J. (2012) Visceral Leishmaniasis Treatment: What Do We Have, What Do We Need and How To Deliver It? International Journal for Parasitology: Drugs and Drug Resistance, 2, 11-19. http://dx.doi.org/10.1016/j.ijpddr.2012.01.003
Lemos. P., Dantas-Torresa, F., da Silva, F., Veloso, V., Gaudêncioa, K. and Brandao-Filhoa, S. (2013) Ecology of Lutzomyia longipalpis in an Area of Visceral Leishmaniasis Transmission in North-Eastern Brazil. Acta Tropica, 126, 99-102. http://dx.doi.org/10.1016/j.actatropica.2013.01.011
Montoya-Lerma, J., Cadena, H., Oviedo, M., Ready, P., Barazarte, R., Travi, B. and Lane, R. (2003) Comparative Vectorial Efficiency of Lutzomyia evansi and Lu. longipalpis for Transmitting Leishmania chagasi. Acta Tropica, 85, 19-29. http://dx.doi.org/10.1016/S0001-706X(02)00189-4
Rangel, E. and Vilela, M. (2008) Lutzomyia longipalpis (Diptera, Psychodidae, Phlebotominae) and Urbanization of Visceral Leishmaniasis in Brazil. Cadernos de Saúde Pública, 24, 2948-2952. http://dx.doi.org/10.1590/S0102-311X2008001200025
Desjeux, P. (2004) Leishmaniasis: Current Situation and New Perspectives. Comparative Immunology, Microbiology & Infectious Diseases, 27, 305-318. http://dx.doi.org/10.1016/j.cimid.2004.03.004
Raffa, K., Adams, A., Broderick, N., Boone, C., Cardoza, Y., Delalibera, I. and Vasanthakumar, A. (2008) Symbionts of Invasive Insects: Characterization, Ecological Roles, and Relation to Invasive Potential and Management Strategies. Department of Entomology, University of Wisconsin-Madison, Madison, 61-62.
Shanchez-Contreras, M. and Vlisidou, I. (2008) The Diversity of Insect-Bacteria Interactions and Its Applications for Disease Control. Biotechnology and Genetic Engineering, 25, 203-244. http://dx.doi.org/10.5661/bger-25-203
Antibiotic Susceptibility
Azambuja, P., Garcia, E. and Ratcliffe, N. (2005) Gut Microbiota and Parasite Transmission by Insect Vectors. Trends in Parasitology, 21, 568-572. http://dx.doi.org/10.1016/j.pt.2005.09.011
Sant’anna, M., Darby, A., Brazil, R., Montoya, J., Dillon, V., et al. (2012) Investigation of the Bacterial Communities Associated with Females of Lutzomyia Sand Fly Species from South America. PLoS ONE, 7, e42531. http://dx.doi.org/10.1371/journal.pone.0042531
Moraes, A., Sergio, H., et al. (2008) Leishmania (Leishmania) chagasi Interactions with Serratia marcescens: Ultrastructural Studies, Lysis and Carbohydrate Effects. Experimental Parasitology, 118, 561-568. http://dx.doi.org/10.1016/j.exppara.2007.11.015
Boulanger, N., Lowenberger, C., Volf, P., et al. (2004) Characterization of a Defensin from the Sand Fly Phlebotomus duboscqi Induced by Challenge with Bacteria or the Protozoan Parasite Leishmania major. Infection and Immunity, 72, 7140-7146. http://dx.doi.org/10.1128/IAI.72.12.7140-7146.2004
Días, H., Sant’anna, M. and Genta, F. (2012) Reactive Oxygen Species-Mediated Immunity against Leishmania mexicana and Serratia marcescens in the Phlebotomine Sand Fly Lutzomyia longipalpis. The Journal of Biological Chemistry, 287, 23995-24003. http://dx.doi.org/10.1074/jbc.M112.376095
Sant’Anna, M., Diaz-Albiter, H., Aguiar, K., et al. (2014) Colonisation Resistance in the Sand Fly Gut: Leishmania Protects Lutzomyia longipalpis from Bacterial Infection. Parasites & Vectors, 7, 329. http://dx.doi.org/10.1186/1756-3305-7-329
González, C., Cabrera, O., Munstermann, L. and Ferro, C. (2006) Distribución de los vectores de Leishmania infantum (Kinetoplastida: Trypanosomatidae) en Colombia. Biomédica, 26, 64-72. http://dx.doi.org/10.7705/biomedica.v26i1.1501
Vivero, R., Torres-Gutierrez, C., Bejarano, E., Estrada, L., Florez, F., et al. (2009) Nuevos registros de flebotomíneos (Diptera: Psychodidae), con el hallazgo de Lutzomyia longipalpis (Lutz & Neiva, 1912), en los alrededores de la Ciudad de Sincelejo, Colombia. Biota Neotropica, 9, 277-280. http://dx.doi.org/10.1590/S1676-06032009000400031
Pulido, S., Munoz, D., Restrepo, A., Mesa, C., Alzate, J., Vélez, I. and Robledo, S. (2011) Improvement of the Green Fluorescent Protein Reporter System in Leishmania spp. for the in Vitro and in Vivo Screening of Antileishmanial Drugs. Acta Tropica, 122, 36-45. http://dx.doi.org/10.1016/j.actatropica.2011.11.015
Romero-Tabarez, M., Jansen, R., Sylla, M., Lünsdorf, H., Haussler, S., Santosa, D., et al. (2006) 7-O-Malonyl Macrolactin A, a New Macrolactin Antibiotic from Bacillus subtilis Active against Methicillin-Resistant Staphylococcus aureus, Vancomycin-Resistant Enterococci, and a Small-Colony Variant of Burkholderia cepacia. Antimicrobial Agents and Chemotherapy, 50, 1701-1709. http://dx.doi.org/10.1128/AAC.50.5.1701-1709.2006
Krug, D., Zurek, G., Revermann, O., Vos, M., Velicer, G. and Müller, R. (2008) Discovering the Hidden Secondary Metabolome of Myxococcus xanthus: A Study of Intraspecific Diversity. Applied and Environmental Microbiology, 74, 3058-3068. http://dx.doi.org/10.1128/AEM.02863-07
Sierra-Garcia, I., Romero, M. and Orduz, S. (2012) Determinación de la actividad antimicrobiana e insecticida de extractos producidos por bacterias aisladas de suelo. Actualidades Biológicas, 34, 5-19.
Sangnoi, Y., Srisukchayakul, P., Arunpairojana, V. and Kanjana-Opas, A. (2009) Diversity of Marine Gliding Bacteria in Thailand and Their Cytotoxicity. Electronic Journal of Biotechnology, 12, 1-8.
El-Masry, H., Fahmy, H. and Abdelwahed, A. (2000) Synthesis and Antimicrobial Activity of Some New Benzimidazole Derivatives. Molecules, 5, 1429-1438. http://dx.doi.org/10.3390/51201429
Cona, E. (2002) Condiciones para un buen estudio de susceptibilidad mediante test de difusión en agar. Revista Chilena de Infectología, 19, 77-81. http://dx.doi.org/10.4067/S0716-10182002019200001
Clinical and Laboratory Standards Institute—CLSI (2009) Methods for Dilution Antimicrobial Susceptibility Test for Bacteria That Grow Aerobically. Approved Standard, 29, 1-65.
Maleki-Ravasan, M., Oshaghi, M., Afshar, D., et al. (2015) Aerobic Bacterial Flora of Biotic and Abiotic Compartments of a Hyperendemic Zoonotic Cutaneous Leishmaniasis (ZCL) Focus. Parasites & Vectors, 8, 63. http://dx.doi.org/10.1186/s13071-014-0517-3
Cox, C.R., Coburn, P.S. and Gilmore, M.S. (2005) Enterococcal Cytolysin: A Novel Two Component Peptide System That Serves as a Bacterial Defense against Eukaryotic and Prokaryotic Cells. Current Protein & Peptide Science, 6, 77-84. http://dx.doi.org/10.2174/1389203053027557
Sacks, D., Govind, M., Rowton, E., Spa, G., Epstein, L., Turcoi, S. and Beverley, S. (2000) The Role of Phosphoglycans in Leishmania-Sand Fly Interactions. Proceedings of the National Academy of Sciences of the United States of America, 97, 406-411. http://dx.doi.org/10.1073/pnas.97.1.406
Kamhawi, S. (2006) Phlebotomine Sand Flies and Leishmania Parasites: Friends or Foes? Trends in Parasitology, 22, 439-445. http://dx.doi.org/10.1016/j.pt.2006.06.012
Yadav, K., Bora, A., Datta, S., et al. (2015) Molecular Characterization of Midgut Microbiota of Aedes albopictus and Aedes aegypti from Arunachal Pradesh, India. Parasites & Vectors, 8, 641. http://dx.doi.org/10.1186/s13071-015-1252-0
Akhoundi, M., Bakhtiari, R., Guillard, T., Baghaei, A., Tolouei, R., Sereno, D., et al. (2012) Diversity of the Bacterial and Fungal Microflora from the Midgut and Cuticle of Phlebotomine Sand Flies Collected in North-Western Iran. PLoS ONE, 7, e50259. http://dx.doi.org/10.1371/journal.pone.0050259
Bonaterra, A., Badosa, E., Rezzonico, F., Duffy, B. and Montesinos, E. (2014) Phenotypic Comparison of Clinical and Plant-Beneficial Strains of Pantoea agglomerans. International Microbiology, 17, 81-90.
Maayer, D., Chan, W., Rubagotti, E., Venter, E., Toth, I., Birch, P. and Coutinho, C. (2014) Analysis of the Pantoea ananatis Pan-Genome Reveals Factors Underlying Its Ability to Colonize and Interact with Plant, Insect and Vertebrate Hosts. BMC Genomics, 15, 404. http://www.biomedcentral.com/1471-2164/15/404
Bisi, D. and Lampe, D. (2011) Secretion of Anti-Plasmodium Effector Proteins from a Natural Pantoea agglomerans Isolated by Using PelB and HlyA Secretion Signals. Applied and Environmental Microbiology, 77, 4669-4675. http://dx.doi.org/10.1128/AEM.00514-11
Volf, P., Kiewegová, A. and Nemec, A. (2002) Bacterial Colonisation in the Gut of Phlebotomus dubosqi (Diptera: Psychodidae): Transtadial Passage and the Role of Female Diet. Folia Parasitologica, 49, 73-77. http://dx.doi.org/10.14411/fp.2002.014
Vallet-Gely, I., Lemaitre, B. and Boccard, F. (2008) Bacterial Strategies to Overcome Insect Defences. Nature, 6, 302-313. http://dx.doi.org/10.1038/nrmicro1870
Shyntum, D., Theron, J., Venter, S., Moleleki, L., Toth, I. and Coutinho, T. (2015) Pantoea ananatis Utilizes a Type VI Secretion System for Pathogenesis and Bacterial Competition. Molecular Plant-Microbe Interactions, 28, 420-431. http://dx.doi.org/10.1094/MPMI-07-14-0219-R
Holland, B. (2010) The Extraordinary Diversity of Bacterial Protein Secretion Mechanisms. In: Economou, A., Ed., Protein Secretion Methods and Protocols, Humana Press, New York, 1-20. http://dx.doi.org/10.1007/978-1-60327-412-8_1
Riley, M., Goldtone, C., Wertz, J. and Gordon, D. (2003) A Phylogenetic Approach to Assessing the Targets of Microbial Warfare. Journal of Evolutionary Biology, 16, 690-697. http://dx.doi.org/10.1046/j.1420-9101.2003.00575.x
Mandal, S., Sharma, S., Pinnaka, K., Kumari, A. and Korpole, S. (2013) Isolation and Characterization of Diverse Antimicrobial Lipopeptides Produced by Citrobacter and Enterobacter. BMC Microbiology, 13, 152. http://dx.doi.org/10.1186/1471-2180-13-152
Seleem, M., Ali, M., Boyle, S., et al. (2006) Establishment of a Gene Expression System in Ochrobactrum anthropi. Applied and Environmental Microbiology, 72, 6833-6836. http://dx.doi.org/10.1128/AEM.01446-06
Bergman, J. (2003) Does the Acquisition of Antibiotic and Pesticide Resistance Provide Evidence for Evolution? Journal of Creation, 17, 26-32.
Ogawa, J., Takeda, S., Xie, S., et al. (2001) Purification, Characterization, and Gene Cloning of Purine Nucleosidase from Ochrobactrum anthropi. Applied and Environmental Microbiology, 67, 1783-1787. http://dx.doi.org/10.1128/AEM.67.4.1783-1787.2001
Tamburro, A., Robuffo, I., Heipieper, H., et al. (2004) Expression of Glutathione S-Transferase and Peptide Methionine Sulphoxide Reductase in Ochrobactrum anthropi Is Correlated to the Production of Reactive Oxygen Species Caused by Aromatic Substrates. FEMS Microbiology Letters, 241, 151-156. http://dx.doi.org/10.1016/j.femsle.2004.10.013
Higgins, C., Murtough, S., Williamson, E., Hiom, S. and Payne, D. (2001) Biocides among Non-Fermenting Gram-Negative Bacteria. Clinical Microbiology and Infection, 7, 308-315. http://dx.doi.org/10.1046/j.1198-743x.2001.00253.x
Vay, C., Almuzara, M., Rodríguez, C., Pugliese, M., Barba, F., Mattera, J. and Famiglietti, A. (2005) Actividad “in Vitro” de diferentes antibacterianos sobre bacilos gram-negativos no fermentadores, excluidos Pseudomonas aeruginosa y Acinetobacter spp. Revista Argentina de Microbiología, 37, 34-45.
Nadjar, D., Labia, R., Cerceau, C., Bizet, C., Philippon, A. and Arlet, G. (2001) Molecular Characterization of Chromosomal Class C β-Lactamase and Its Regulatory Gene in Ochrobactrum anthropi. Antimicrobial Agents and Chemotherapy, 45, 2324-2330. http://dx.doi.org/10.1128/AAC.45.8.2324-2330.2001
Duran, R., Vatansever, U., Acunas, B. and Basaran, U. (2009) Ochrobactrum anthropi Bacteremia in a Preterm Infant with Meconium Peritonitis. International Journal of Infectious Diseases, 2, 61-63. http://dx.doi.org/10.1016/j.ijid.2008.06.027
Fernández-Fuentes, M., Morente, E., Abriouel, H., Pulido, R. and Gálvez, A. (2012) Isolation and Identification of Bacteria from Organic Foods: Susceptibility to Biocides and Antibiotics. Food Control, 26, 73-78. http://dx.doi.org/10.1016/j.foodcont.2012.01.017