Photorhabdus Spp.: an Overview of the Beneficial Aspects of Mutualistic Bacteria of Insecticidal Nematodes
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Genetics and Physiology of Motility by Photorhabdus Spp Brandye A
University of New Hampshire University of New Hampshire Scholars' Repository Doctoral Dissertations Student Scholarship Spring 2006 Genetics and physiology of motility by Photorhabdus spp Brandye A. Michaels University of New Hampshire, Durham Follow this and additional works at: https://scholars.unh.edu/dissertation Recommended Citation Michaels, Brandye A., "Genetics and physiology of motility by Photorhabdus spp" (2006). Doctoral Dissertations. 324. https://scholars.unh.edu/dissertation/324 This Dissertation is brought to you for free and open access by the Student Scholarship at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. GENETICS AND PHYSIOLOGY OF MOTILITY BYPHOTORHABDUS SPP. BY BRANDYE A. MICHAELS BS, Armstrong Atlantic State University, 1999 DISSERTATION Submitted to the University of New Hampshire in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Microbiology May, 2006 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. UMI Number: 3217433 INFORMATION TO USERS The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleed-through, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. ® UMI UMI Microform 3217433 Copyright 2006 by ProQuest Information and Learning Company. -
1 Caracterización Molecular Y
Tropical and Subtropical Agroecosystems 23 (2020): #64 Grifaldo-Alcantara et al., 2020 CARACTERIZACIÓN MOLECULAR Y MORFOMÉTRICA DE Heterorhabditis indica (CEPA CP13JA) AISLADO EN EL CULTIVO DE CAÑA DE AZÚCAR † [MOLECULAR AND MORPHOMETRIC CHARACTERIZATION OF Heterorhabditis indica (STRAIN CP13JA) ISOLATED IN THE CULTIVATION SUGARCANE] Pedro Fabian Grifaldo-Alcantara1, Raquel Alatorre-Rosas2, Hilda Victoria Silva-Rojas2, Patricia S. Stock3, Francisco Hernandez-Rosas4, Haidel Vargas-Madriz1, Ausencio Azuara-Dominguez5 and Yuridia Durán-Trujillo6 * 1 Centro Universitario de la Costa Sur, Universidad de Guadalajara, Departamento de Producción Agrícola. Av. Independencia Nacional # 151, Autlán de Navarro, Jalisco, C.P. 48900, México. Email. [email protected], [email protected] 2 Colegio de Postgraduados, Campus Montecillo, Km. 36.5 carretera México- Texcoco, Montecillo, Texcoco, Edo de México, México. C.P. 56230. Email. [email protected], [email protected] 3 University of Arizona, Department of Entomology / Plant Sciences. Forbes Bldg. Km 410. 1140 E. South Campus Tucson, AZ. USA. Email. [email protected] 4 Colegio de Postgraduados, Campus Córdoba, Km 348 carretera Federal Córdoba- Veracruz, Amatlán de los Reyes, Veracruz, México. C.P. 94946. México. Email. [email protected] 5 Tecnológico Nacional de México/I.T. de Cd. Victoria, Ciudad Victoria, Tamaulipas, CP 87010 México. Email. [email protected] 6 Universidad Autónoma de Guerrero, Facultad de Ciencias Agropecuarias y Ambientales. Periférico Poniente S/N Frente a la Colonia Villa de Guadalupe, Iguala de la independencia, Guerrero, México, CP 40040. Email. [email protected] *Corresponding author SUMMARY Background. Heterorhabditis and Steinernema are two genera of entomopathogen nematodes used as effective biocontrollers in pest insect control. Target. -
Evolutionary Patchwork of an Insecticidal Toxin
Ruffner et al. BMC Genomics (2015) 16:609 DOI 10.1186/s12864-015-1763-2 RESEARCH ARTICLE Open Access Evolutionary patchwork of an insecticidal toxin shared between plant-associated pseudomonads and the insect pathogens Photorhabdus and Xenorhabdus Beat Ruffner1, Maria Péchy-Tarr2, Monica Höfte3, Guido Bloemberg4, Jürg Grunder5, Christoph Keel2* and Monika Maurhofer1* Abstract Background: Root-colonizing fluorescent pseudomonads are known for their excellent abilities to protect plants against soil-borne fungal pathogens. Some of these bacteria produce an insecticidal toxin (Fit) suggesting that they may exploit insect hosts as a secondary niche. However, the ecological relevance of insect toxicity and the mechanisms driving the evolution of toxin production remain puzzling. Results: Screening a large collection of plant-associated pseudomonads for insecticidal activity and presence of the Fit toxin revealed that Fit is highly indicative of insecticidal activity and predicts that Pseudomonas protegens and P. chlororaphis are exclusive Fit producers. A comparative evolutionary analysis of Fit toxin-producing Pseudomonas including the insect-pathogenic bacteria Photorhabdus and Xenorhadus, which produce the Fit related Mcf toxin, showed that fit genes are part of a dynamic genomic region with substantial presence/absence polymorphism and local variation in GC base composition. The patchy distribution and phylogenetic incongruence of fit genes indicate that the Fit cluster evolved via horizontal transfer, followed by functional integration of vertically transmitted genes, generating a unique Pseudomonas-specific insect toxin cluster. Conclusions: Our findings suggest that multiple independent evolutionary events led to formation of at least three versions of the Mcf/Fit toxin highlighting the dynamic nature of insect toxin evolution. -
Identification of Photorhabdus Symbionts by MALDI-TOF Mass Spectrometry
bioRxiv preprint doi: https://doi.org/10.1101/2020.01.10.901900; this version posted January 11, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Identification of Photorhabdus symbionts by MALDI-TOF mass spectrometry Virginia Hill1,2, Peter Kuhnert2, Matthias Erb1, Ricardo A. R. Machado1* 1 Institute of Plant Sciences, University of Bern, Switzerland 2Institute of Veterinary Bacteriology, Vetsuisse Faculty, University of Bern, Switzerland. *Correspondence: [email protected] Abstract Species of the bacterial genus Photorhabus live in a symbiotic relationship with Heterorhabditis entomopathogenic nematodes. Besides their use as biological control agents against agricultural pests, some Photorhabdus species are also a source of natural products and are of medical interest due to their ability to cause tissue infections and subcutaneous lesions in humans. Given the diversity of Photorhabdus species, rapid and reliable methods to resolve this genus to the species level are needed. In this study, we evaluated the potential of matrix-assisted laser desorption/ionization time-of flight mass spectrometry (MALDI-TOF MS) for the identification of Photorhabdus species. To this end, we established a collection of 55 isolates consisting of type strains and multiple field strains that belong to each of the validly described species and subspecies of this genus. Reference spectra for the strains were generated and used to complement a currently available database. The extended reference database was then used for identification based on the direct transfer and protein fingerprint of single colonies. -
The Louse Fly-Arsenophonus Arthropodicus Association
THE LOUSE FLY-ARSENOPHONUS ARTHROPODICUS ASSOCIATION: DEVELOPMENT OF A NEW MODEL SYSTEM FOR THE STUDY OF INSECT-BACTERIAL ENDOSYMBIOSES by Kari Lyn Smith A dissertation submitted to the faculty of The University of Utah in partial fulfillment of the requirements for the degree of Doctor of Philosophy Department of Biology The University of Utah August 2012 Copyright © Kari Lyn Smith 2012 All Rights Reserved The University of Utah Graduate School STATEMENT OF DISSERTATION APPROVAL The dissertation of Kari Lyn Smith has been approved by the following supervisory committee members: Colin Dale Chair June 18, 2012 Date Approved Dale Clayton Member June 18, 2012 Date Approved Maria-Denise Dearing Member June 18, 2012 Date Approved Jon Seger Member June 18, 2012 Date Approved Robert Weiss Member June 18, 2012 Date Approved and by Neil Vickers Chair of the Department of __________________________Biology and by Charles A. Wight, Dean of The Graduate School. ABSTRACT There are many bacteria that associate with insects in a mutualistic manner and offer their hosts distinct fitness advantages, and thus have likely played an important role in shaping the ecology and evolution of insects. Therefore, there is much interest in understanding how these relationships are initiated and maintained and the molecular mechanisms involved in this process, as well as interest in developing symbionts as platforms for paratransgenesis to combat disease transmission by insect hosts. However, this research has been hampered by having only a limited number of systems to work with, due to the difficulties in isolating and modifying bacterial symbionts in the lab. In this dissertation, I present my work in developing a recently described insect-bacterial symbiosis, that of the louse fly, Pseudolynchia canariensis, and its bacterial symbiont, Candidatus Arsenophonus arthropodicus, into a new model system with which to investigate the mechanisms and evolution of symbiosis. -
Monophyly of Clade III Nematodes Is Not Supported by Phylogenetic Analysis of Complete Mitochondrial Genome Sequences
UC Davis UC Davis Previously Published Works Title Monophyly of clade III nematodes is not supported by phylogenetic analysis of complete mitochondrial genome sequences Permalink https://escholarship.org/uc/item/7509r5vp Journal BMC Genomics, 12(1) ISSN 1471-2164 Authors Park, Joong-Ki Sultana, Tahera Lee, Sang-Hwa et al. Publication Date 2011-08-03 DOI http://dx.doi.org/10.1186/1471-2164-12-392 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Park et al. BMC Genomics 2011, 12:392 http://www.biomedcentral.com/1471-2164/12/392 RESEARCHARTICLE Open Access Monophyly of clade III nematodes is not supported by phylogenetic analysis of complete mitochondrial genome sequences Joong-Ki Park1*, Tahera Sultana2, Sang-Hwa Lee3, Seokha Kang4, Hyong Kyu Kim5, Gi-Sik Min2, Keeseon S Eom6 and Steven A Nadler7 Abstract Background: The orders Ascaridida, Oxyurida, and Spirurida represent major components of zooparasitic nematode diversity, including many species of veterinary and medical importance. Phylum-wide nematode phylogenetic hypotheses have mainly been based on nuclear rDNA sequences, but more recently complete mitochondrial (mtDNA) gene sequences have provided another source of molecular information to evaluate relationships. Although there is much agreement between nuclear rDNA and mtDNA phylogenies, relationships among certain major clades are different. In this study we report that mtDNA sequences do not support the monophyly of Ascaridida, Oxyurida and Spirurida (clade III) in contrast to results for nuclear rDNA. Results from mtDNA genomes show promise as an additional independently evolving genome for developing phylogenetic hypotheses for nematodes, although substantially increased taxon sampling is needed for enhanced comparative value with nuclear rDNA. -
Comparison of Xenorhabdus Bovienii Bacterial Strain Genomes Reveals Diversity in Symbiotic Functions Kristen E
Murfin et al. BMC Genomics (2015) 16:889 DOI 10.1186/s12864-015-2000-8 RESEARCH ARTICLE Open Access Comparison of Xenorhabdus bovienii bacterial strain genomes reveals diversity in symbiotic functions Kristen E. Murfin1, Amy C. Whooley1, Jonathan L. Klassen2 and Heidi Goodrich-Blair1* Abstract Background: Xenorhabdus bacteria engage in a beneficial symbiosis with Steinernema nematodes, in part by providing activities that help kill and degrade insect hosts for nutrition. Xenorhabdus strains (members of a single species) can display wide variation in host-interaction phenotypes and genetic potential indicating that strains may differ in their encoded symbiosis factors, including secreted metabolites. Methods: To discern strain-level variation among symbiosis factors, and facilitate the identification of novel compounds, we performed a comparative analysis of the genomes of 10 Xenorhabdus bovienii bacterial strains. Results: The analyzed X. bovienii draft genomes are broadly similar in structure (e.g. size, GC content, number of coding sequences). Genome content analysis revealed that general classes of putative host-microbe interaction functions, such as secretion systems and toxin classes, were identified in all bacterial strains. In contrast, we observed diversity of individual genes within families (e.g. non-ribosomal peptide synthetase clusters and insecticidal toxin components), indicating the specific molecules secreted by each strain can vary. Additionally, phenotypic analysis indicates that regulation of activities (e.g. enzymes and motility) differs among strains. Conclusions: The analyses presented here demonstrate that while general mechanisms by which X. bovienii bacterial strains interact with their invertebrate hosts are similar, the specific molecules mediating these interactions differ. Our data support that adaptation of individual bacterial strains to distinct hosts or niches has occurred. -
Distribution of Entomopathogenic Nematodes of the Genus Heterorhabditis (Rhabditida: Heterorhabditidae) in Bulgaria
13 Gradinarov_173 7-01-2013 9:34 Pagina 173 Nematol. medit. (2012), 40: 173-180 173 DISTRIBUTION OF ENTOMOPATHOGENIC NEMATODES OF THE GENUS HETERORHABDITIS (RHABDITIDA: HETERORHABDITIDAE) IN BULGARIA D. Gradinarov1*, E. Petrova**, Y. Mutafchiev***, O. Karadjova** * Department of Zoology and Anthropology, Faculty of Biology, Sofia University “St. Kliment Ohridski”, 8 Dragan Tzankov Blvd., 1164 Sofia, Bulgaria ** Institute of Soil Science, Agrotechnology and Plant Protection “N. Pushkarov”, Division of Plant Protection, Kostinbrod, Bulgaria *** Institute of Biodiversity and Ecosystem Research, 2 Gagarin Str., 1113 Sofia, Bulgaria Received: 21 September 2012; Accepted: 21 November 2012. Summary. The results from studies on entomopathogenic nematodes of the genus Heterorhabditis Poinar, 1976 (Rhabditida: Het- erorhabditidae) in Bulgaria, conducted during 1994-2010 are summarized. Of the 1,227 soil samples collected, 3.5% were positive for the presence of Heterorhabditis spp. Specimens belonging to the genus were obtained from 43 soil samples collected at 27 lo- calities in different regions of the country. Heterorhabditids were established at altitudes from 0 to 1175 m, in habitats both along the Black Sea coast and inland. The prevalent species was H. bacteriophora Poinar, 1976. Its identity was confirmed by detailed morphometric studies and molecular analyses of four recently obtained isolates. Inland, H. bacteriophora prefers alluvial soils in river valleys under herbaceous and woody vegetation. It was also found in calcareous soils with pronounced fluctuations in the temperature and water conditions. The presence of the species H. megidis Poinar, Jackson et Klein, 1987 in Bulgaria needs further confirmation. Key words: Heterorhabditis bacteriophora, morphology, molecular identification, habitat preferences. Entomopathogenic nematodes (EPNs) (Rhabditida: processing of 1,227 soil samples collected during the pe- Steinernematidae, Heterorhabditidae) are obligate para- riod November, 1994 to October, 2010 from different sites of a wide range of soil insects. -
Entomopathogenic Nematodes (Nematoda: Rhabditida: Families Steinernematidae and Heterorhabditidae) 1 Nastaran Tofangsazi, Steven P
EENY-530 Entomopathogenic Nematodes (Nematoda: Rhabditida: families Steinernematidae and Heterorhabditidae) 1 Nastaran Tofangsazi, Steven P. Arthurs, and Robin M. Giblin-Davis2 Introduction Entomopathogenic nematodes are soft bodied, non- segmented roundworms that are obligate or sometimes facultative parasites of insects. Entomopathogenic nema- todes occur naturally in soil environments and locate their host in response to carbon dioxide, vibration, and other chemical cues (Kaya and Gaugler 1993). Species in two families (Heterorhabditidae and Steinernematidae) have been effectively used as biological insecticides in pest man- agement programs (Grewal et al. 2005). Entomopathogenic nematodes fit nicely into integrated pest management, or IPM, programs because they are considered nontoxic to Figure 1. Infective juvenile stages of Steinernema carpocapsae clearly humans, relatively specific to their target pest(s), and can showing protective sheath formed by retaining the second stage be applied with standard pesticide equipment (Shapiro-Ilan cuticle. et al. 2006). Entomopathogenic nematodes have been Credits: James Kerrigan, UF/IFAS exempted from the US Environmental Protection Agency Life Cycle (EPA) pesticide registration. There is no need for personal protective equipment and re-entry restrictions. Insect The infective juvenile stage (IJ) is the only free living resistance problems are unlikely. stage of entomopathogenic nematodes. The juvenile stage penetrates the host insect via the spiracles, mouth, anus, or in some species through intersegmental membranes of the cuticle, and then enters into the hemocoel (Bedding and Molyneux 1982). Both Heterorhabditis and Steinernema are mutualistically associated with bacteria of the genera Photorhabdus and Xenorhabdus, respectively (Ferreira and 1. This document is EENY-530, one of a series of the Department of Entomology and Nematology, UF/IFAS Extension. -
Comparative Phenotypic and Genomics Approaches
Comparative Phenotypic and Genomics Approaches Provide Insight into the Tripartite Symbiosis of Xenorhabdus bovienii with Steinernema Nematode and Lepidopteran Insect Hosts Item Type text; Electronic Thesis Authors McMullen, John George II Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 25/09/2021 05:58:01 Link to Item http://hdl.handle.net/10150/596124 COMPARATIVE PHENOTYPIC AND GENOMICS APPROACHES PROVIDE INSIGHT INTO THE TRIPARTITE SYMBIOSIS OF XENORHABDUS BOVIENII WITH STEINERNEMA NEMATODE AND LEPIDOPTERAN INSECT HOSTS by John George McMullen II ____________________________ A Thesis Submitted to the Faculty of the SCHOOL OF ANIMAL AND COMPARATIVE BIOMEDICAL SCIENCES In Partial Fulfillment of the Requirements For the Degree of MASTER OF SCIENCE In the Graduate College THE UNIVERSITY OF ARIZONA 2015 STATEMENT BY AUTHOR This thesis has been submitted in partial fulfillment of requirements for an advanced degree at the University of Arizona and is deposited in the University Library to be made available to borrowers under rules of the Library. Brief quotations from this thesis are allowable without special permission, provided that an accurate acknowledgement of the source is made. Requests for permission for extended quotation from or reproduction of this manuscript in whole or in part may be granted by the head of the major department or the Dean of the Graduate College when in his or her judgment the proposed use of the material is in the interests of scholarship. -
Nematodes As Biocontrol Agents This Page Intentionally Left Blank Nematodes As Biocontrol Agents
Nematodes as Biocontrol Agents This page intentionally left blank Nematodes as Biocontrol Agents Edited by Parwinder S. Grewal Department of Entomology Ohio State University, Wooster, Ohio USA Ralf-Udo Ehlers Department of Biotechnology and Biological Control Institute for Phytopathology Christian-Albrechts-University Kiel, Raisdorf Germany David I. Shapiro-Ilan United States Department of Agriculture Agriculture Research Service Southeastern Fruit and Tree Nut Research Laboratory, Byron, Georgia USA CABI Publishing CABI Publishing is a division of CAB International CABI Publishing CABI Publishing CAB International 875 Massachusetts Avenue Wallingford 7th Floor Oxfordshire OX10 8DE Cambridge, MA 02139 UK USA Tel: þ44 (0)1491 832111 Tel: þ1 617 395 4056 Fax: þ44 (0)1491 833508 Fax: þ1 617 354 6875 E-mail: [email protected] E-mail: [email protected] Web site: www.cabi-publishing.org ßCAB International 2005. All rights reserved. No part of this publication may be reproduced in any form or by any means, electronically, mech- anically, by photocopying, recording or otherwise, without the prior permission of the copyright owners. A catalogue record for this book is available from the British Library, London, UK. Library of Congress Cataloging-in-Publication Data Nematodes as biocontrol agents / edited by Parwinder S. Grewal, Ralf- Udo Ehlers, David I. Shapiro-Ilan. p. cm. Includes bibliographical references and index. ISBN 0-85199-017-7 (alk. paper) 1. Nematoda as biological pest control agents. I. Grewal, Parwinder S. II. Ehlers, Ralf-Udo. III. Shaprio-Ilan, David I. SB976.N46N46 2005 632’.96–dc22 2004030022 ISBN 0 85199 0177 Typeset by SPI Publisher Services, Pondicherry, India Printed and bound in the UK by Biddles Ltd., King’s Lynn This volume is dedicated to Dr Harry K. -
JOURNAL of NEMATOLOGY Article | DOI: 10.21307/Jofnem-2020-089 E2020-89 | Vol
JOURNAL OF NEMATOLOGY Article | DOI: 10.21307/jofnem-2020-089 e2020-89 | Vol. 52 Isolation, identification, and pathogenicity of Steinernema carpocapsae and its bacterial symbiont in Cauca-Colombia Esteban Neira-Monsalve1, Natalia Carolina Wilches-Ramírez1, Wilson Terán1, María del Pilar Abstract 1 Márquez , Ana Teresa In Colombia, identification of entomopathogenic nematodes (EPN’s) 2 Mosquera-Espinosa and native species is of great importance for pest management 1, Adriana Sáenz-Aponte * programs. The aim of this study was to isolate and identify EPNs 1Biología de Plantas y Sistemas and their bacterial symbiont in the department of Cauca-Colombia Productivos, Departamento de and then evaluate the susceptibility of two Hass avocado (Persea Biología, Pontificia Universidad americana) pests to the EPNs isolated. EPNs were isolated from soil Javeriana, Bogotá, Colombia. samples by the insect baiting technique. Their bacterial symbiont was isolated from hemolymph of infected Galleria mellonella larvae. 2 Departamento de Ciencias Both organisms were molecularly identified. Morphological, and Naturales y Matemáticas, biochemical cha racterization was done for the bacteria. Susceptibility Pontificia Universidad Javeriana, of Epitrix cucumeris and Pandeleteius cinereus adults was evaluated Cali, Colombia. by individually exposing adults to 50 infective juveniles. EPNs were *E-mail: adriana.saenz@javeriana. allegedly detected at two sampled sites (natural forest and coffee edu.co cultivation) in 5.8% of the samples analyzed. However, only natural forest EPN’s could be isolated and multiplied. The isolate was identified This paper was edited by as Steinernema carpocapsae BPS and its bacterial symbiont as Raquel Campos-Herrera. Xenorhabus nematophila BPS. Adults of both pests were susceptible Received for publication to S.