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Introduction to Practical Phytobacteriology PDF

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CCCCCooooonnnnnttttteeeeennnnntttttsssss A SAFRINET MANUAL FOR PHYTOBACTERIOLOGY (cid:1)(cid:2)(cid:3)(cid:4)(cid:5)(cid:6)(cid:7)(cid:8)(cid:3)(cid:9)(cid:5)(cid:2)(cid:10) (cid:3)(cid:5) (cid:11)(cid:4)(cid:12)(cid:8)(cid:3)(cid:9)(cid:8)(cid:12)(cid:13) (cid:11)(cid:14)(cid:15)(cid:3)(cid:5)(cid:16)(cid:12)(cid:8)(cid:3)(cid:17)(cid:4)(cid:9)(cid:5)(cid:13)(cid:5)(cid:18)(cid:15) CCCCCooooommmmmpppppiiiiillllleeeeeddddd bbbbbyyyyy TTTTT..... GGGGGooooossssszzzzzccccczzzzzyyyyynnnnnssssskkkkkaaaaa,,,,, JJJJJ.....JJJJJ..... SSSSSeeeeerrrrrfffffooooonnnnnttttteeeeeiiiiinnnnn &&&&& SSSSS..... SSSSSeeeeerrrrrfffffooooonnnnnttttteeeeeiiiiinnnnn BBBBBaaaaacccccttttteeeeerrrrriiiiiaaaaalllll DDDDDiiiiissssseeeeeaaaaassssseeeeesssss UUUUUnnnnniiiiittttt,,,,, AAAAARRRRRCCCCC–––––PPPPPPPPPPRRRRRIIIII,,,,, SSSSSooooouuuuuttttthhhhh AAAAAfffffrrrrriiiiicccccaaaaa Sponsored by SDC, Switzerland Introduction to Practical Phytobacteriology A Manual for Phytobacteriology by SAFRINET, the Southern African (SADC) LOOP of BioNET-INTERNATIONAL Compiled by T. Goszczynska, J.J. Serfontein & S. Serfontein Bacterial Diseases Unit ARC – Plant Protection Research Institute Pretoria, South Africa Sponsored by The Swiss Agency for Development and Cooperation (SDC) © SAFRINET 2000 c/o ARC - Plant Protection Research Institute Private Bag X134, Pretoria, 0001 South Africa ISBN 0-620-25487-4 First edition, first impression No part of this publication may be reproduced in any form or by any means, including photocopying and recording, without prior permission from the publisher. Layout, design, technical editing & production Isteg Scientific Publications, Irene Imageset by Future Graphics, Centurion Printed by Ultra Litho (Pty) Ltd, Heriotdale, Johannesburg P reface This manual is a guide to a course in practical phytobacteriology for technical assistants of SADC countries in the SAFRINET-LOOP of BioNET-INTERNATIONAL. The course, presented by the staff of the Bacterial Diseases Unit of the ARC - Plant Protection Research Institute, comprises lectures, practical sessions and discussions aimed at teaching students to recognise and identify bacterial diseases of agricultural crops. Techniques to isolate and identify plant-pathogenic bacteria are presented, as well as information on how to preserve isolated pathogens for further study. The manual not only provides technical details but also lists the literature, including books and manuals, that should be available in laboratories specialising in phytobacteriology. A cknowledgements • Sincere thanks are due to Drs Connal Eardley and Elize Lubbe for guidance and advice and to Dr S.H. Koch for her help in compiling a list of bacterial diseases of vegetable crops. (cid:127) Generous funding by the sponsor, The Swiss Agency for Development and Cooperation (SDC), is greatly appreciated. (cid:127) We thank Mr H. Boroko for technical help. Contributing authors T. Goszczynska J.J. Serfontein S. Serfontein (cid:127) Illustrated by Teresa Goszczynska and Elsa van Niekerk. (cid:127) Cover design by Elsa van Niekerk and Nico Dippenaar. (cid:127) Photographs by Kobus (J.J.) Serfontein and Jacomina Bloem. C ontents Preface ... iii Acknowledgements ... iv Introduction .........................................................1 Identification of bacterial plant diseases .....................3 Visual examination and gathering of information . . . . . . . . . . . . . . . . . . . . . . . .3 Testing for bacterial streaming . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4 Isolation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 Colony appearance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 Microscopic examination of isolated bacteria. . . . . . . . . . . . . . . . . . . . . . . . . . .9 Tests for characterisation of bacteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .13 » Utilisation and decomposition of carbon sources . . . . . . . . . . . . . . 13 » Decomposition of nitrogenous compounds . . . . . . . . . . . . . . . . . 14 » Decomposition of macromolecules. . . . . . . . . . . . . . . . . . . . . 15 » Other tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 Determination of pathogenicity ................................19 Classification of bacteria ......................................21 Gram-negative bacteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .22 » Gram-negative aerobic rods and cocci . . . . . . . . . . . . . . . . . . 24 » Gram-negative facultatively anaerobic rods . . . . . . . . . . . . . . . . 34 Gram-positive bacteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .36 » Actinomycetes and related organisms . . . . . . . . . . . . . . . . . . . 36 Cell-wall-free procaryotes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .38 Basic keys for the identification of phytopathogenic bacteria.......................................39 Key No. 1 — Bean, pea (pod spot, leaf spot and blight). . . . . . . . . . . . . . . . . .41 Key No. 2 — Cowpea (leaf spot or leaf blight). . . . . . . . . . . . . . . . . . . . . . . . . .43 Key No. 3 — Tomato. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44 Key No. 4 — Tomato (canker and wilt) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .46 Key No. 5 — Potatowilt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .47 Key No. 6 — Soft rots (fruits, tubers, bulbs and leaves). . . . . . . . . . . . . . . . . . . .49 Key No. 7 — Galls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .50 Key No. 8 — Crucifers (leaf spot, black rot, soft rot) . . . . . . . . . . . . . . . . . . . . . .51 Other methods to detect and identify phytopathogenic bacteria.......................................52 Preservation of bacterial cultures ...........................53 Culture collections. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .53 Preservation of bacteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .53 » Short-term storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53 » Long-term storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54 Epidemiology and control of bacterial diseases...........57 Inoculum sources . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .57 » Primary sources. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57 » Secondary sources. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58 » Conclusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59 Media and diagnostic tests ....................................60 Essential laboratory equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .60 Staining of bacteria and KOH solubility test . . . . . . . . . . . . . . . . . . . . . . . . . . . .61 Preparation of culture media. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .61 General isolation media . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .63 Selective media. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .64 Media for characterisation of phytopathogenic bacteria. . . . . . . . . . . . . . . . .68 » Utilisation and decomposition of carbon sources . . . . . . . . . . . . . . 68 » Decomposition of nitrogenous compounds . . . . . . . . . . . . . . . . . 70 » Decomposition of macromolecules. . . . . . . . . . . . . . . . . . . . . 71 » Other tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73 Recommended reading .........................................75 Useful Internet sites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .77 Index to isolation media and diagnostic tests . . . . . . . . . . . . .78 Glossary ...........................................................80 Appendix — Commonbacterialdiseasesofvegetablecrops.................82 I ntroduction Althoughbacteriacausearathersmallproportionofplantdiseases,thisdoesnotmean thatthesediseasesareunimportant.InNorthCarolina,USA,forinstance,Granvilleor bacterialwiltoftobaccocausedsomuchdamagefor30yearsafteritsappearancein 1880thatitforcedbankstoclose,farmstobesoldandtownstodecline.Amorerecent exampleofaseverebacterialdiseaseiswatermelonfruitblotch,whichappearedin watermelon-productionareasoftheUSA.Pendinglawsuitsandtheriskoffuturelitigation forcedmajorseedcompaniestosuspendtheirwatermelonseedsalesintheautumnof 1994. Otherbioticagentsimplicatedinplantdiseasesarefungi,virusesandnematodes; abioticfactorsmayalsoproducedisease-likesymptoms.Aplantabnormalitycannot alwaysbediagnosedsolelybysymptomsasdifferentagentscancausesimilar pathologicalsymptoms(Fig.1).Softrotcanbecausedbyfungiorbacteria;gallsby A B C D Fig.1 Similarsymptomsonbeanplantscausedbydifferentagents: A–virus;B–bacterium; C–pesticide;D–fungus. 2 Introduction fungi,bacteriaandinsects;leafspotbybacteria,virusesandfungi,andwiltdiseasesby fungiandbacteria.Inasingleplantspecies,symptomscausedbydifferentbacteria mayoverlap,forexamplebacterialblightofbeanandfoliarbacterialdiseasesof tomato.Symptomexpressionofaparticulardiseasecanvaryconsiderably,andmaybe influencedbycropcultivar,growthstage,environmentalconditionsandpathogenstrain. Crop-productionmethods,suchasproductionincontrolledenvironmentslike greenhousesandinhydroponics,alsoplayaroleinsymptomexpression.Changesin productionmethodshavealsobroughtpreviouslyunknownandunimportantdiseasesto theforeground. + A preliminary diagnosis of the disease can be made on the basis of symptoms, microscopic examination and a few diagnostic tests. However, accurate diagnosis of the pathogen is always essential. I dentification of bacterial plant diseases Inadiagnosticlaboratorywhereplantmaterialisanalysedforthepresenceofaplant disease,anumberoflogicalstepsmustbefollowedtoidentifythecausalagentofthe diseaseorplantabnormality. Visual examination and gathering of information •Firststep–besureoftheidentityoftheplanttobeanalysed. Besidestheplant’sidentity,asmuchinformationaspossibleonthecropmustbe gathered,forexamplelocationofcrop,methodofcultivation,irrigationmethods, chemicalsapplied,recentclimatic information. (cid:127)Secondstep–familiariseyourself withthesymptoms(Fig.2). Gatherinformationaboutthe distributionofthediseaseinthecrop. Itisimportanttoexamineasmanyof thediseasedplantsaspossible,from earlytoadvancedstagesof symptomdevelopment. (cid:127)Thirdstep–obtaininformationabout allthepossiblediseasesreportedon thecropinthecountryorsubregion. TheAppendixtothismanualandthe IndexofPlantPathogensandthe DiseasesthattheyCauseinCultivated PlantsinSouthAfrica(Gorter1977),which containsthenameofthecrop,alistof pathogensreportedonthecrop,andthe commonnamesofthediseases,aregood startingpointsinallSADCcountries.Notall diseasesareincludedintheIndexanditis advisabletoobtainasmuchinformation aspossiblefromtheliterature.TheDisease CompendiumSeriespublishedbythe AmericanPhytopathologicalSocietyis veryusefulinthisregard.Italsocontains Fig.2 photographsofdiseasesofparticular Symptomscausedbybacteriaonplants. crops.

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