Literature DB >> 11207774

Co-evolution between Frankia populations and host plants in the family Casuarinaceae and consequent patterns of global dispersal.

P Simonet1, E Navarro, C Rouvier, P Reddell, J Zimpfer, Y Dommergues, R Bardin, P Combarro, J Hamelin, A M Domenach, F Gourbière, Y Prin, J O Dawson, P Normand.   

Abstract

Symbioses between the root nodule-forming, nitrogen-fixing actinomycete Frankia and its angiospermous host plants are important in the nitrogen economies of numerous terrestrial ecosystems. Molecular characterization of Frankia strains using polymerase chain reaction/restriction fragment length polymorphism (PCR/RFLP) analyses of the 16S rRNA-ITS gene and of the nifD-nifK spacer was conducted directly on root nodules collected worldwide from Casuarina and Allocasuarina trees. In their native habitats in Australia, host species contained seven distinctive sets of Frankia in seven different molecular phylogenetic groups. Where Casuarina and Allocasuarina trees are newly planted outside Australia, they do not normally nodulate unless Frankia is introduced with the host seedling. Nodules from Casuarina trees introduced outside Australia over the last two centuries were found to contain Frankia from only one of the seven phylogenetic groups associated with the host genus Casuarina in Australia. The phylogenetic group of Frankia found in Casuarina and Allocasuarina trees introduced outside Australia is the only group that has yielded isolates in pure culture, suggesting a greater ability to survive independently of a host. Furthermore, the Frankia species in this group are able to nodulate a wider range of host species than those in the other six groups. In baiting studies, Casuarina spp. are compatible with more Frankia microsymbiont groups than Allocasuarina host spp. adapted to drier soil conditions, and C. equisetifolia has broader microsymbiont compatibility than other Casuarina spp. Some Frankia associated with the nodular rhizosphere and rhizoplan, but not with the nodular tissue, of Australian hosts were able to nodulate cosmopolitan Myrica plants that have broad microsymbiont compatibility and, hence, are a potential host of Casuarinaceae-infective Frankia outside the hosts' native range. The results are consistent with the idea that Frankia symbiotic promiscuity and ease of isolation on organic substrates, suggesting saprophytic potential, are associated with increased microsymbiont ability to disperse and adapt to diverse new environments, and that both genetics and environment determine a host's nodular microsymbiont.

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Year:  1999        PMID: 11207774     DOI: 10.1046/j.1462-2920.1999.00068.x

Source DB:  PubMed          Journal:  Environ Microbiol        ISSN: 1462-2912            Impact factor:   5.491


  15 in total

1.  Host species and habitat affect nodulation by specific Frankia genotypes in two species of Alnus in interior Alaska.

Authors:  Michael Damon Anderson; Roger W Ruess; David D Myrold; D Lee Taylor
Journal:  Oecologia       Date:  2009-04-08       Impact factor: 3.225

2.  Hypervariable spacer regions are good sites for developing specific PCR-RFLP markers and PCR primers for screening actinorhizal symbionts.

Authors:  Rajani Varehese; Vineeta S Chauhan; Arvind K Misra
Journal:  J Biosci       Date:  2003-06       Impact factor: 1.826

3.  Indigenous actinorhizal plants of Australia.

Authors:  Nishath K Ganguli; Ivan R Kennedy
Journal:  J Biosci       Date:  2013-11       Impact factor: 1.826

4.  16S-23S rRNA intergenic spacer region variability in the genus Frankia.

Authors:  Faten Ghodhbane-Gtari; Imen Nouioui; Mohamed Chair; Abdellatif Boudabous; Maher Gtari
Journal:  Microb Ecol       Date:  2010-02-24       Impact factor: 4.552

5.  Diversity of Frankia populations in root nodules of geographically isolated Arizona alder trees in central Arizona (United States).

Authors:  Allana K Welsh; Jeffrey O Dawson; Gerald J Gottfried; Dittmar Hahn
Journal:  Appl Environ Microbiol       Date:  2009-09-04       Impact factor: 4.792

6.  Genetic diversity of Frankia microsymbionts from the relict species Myrica faya (Ait.) and Myrica rivas-martinezii (S.) in Canary Islands and Hawaii.

Authors:  V Huguet; E Ojeda Land; J Garcia Casanova; J F Zimpfer; M P Fernandez
Journal:  Microb Ecol       Date:  2005-07-27       Impact factor: 4.552

7.  Local adaptation of frankia to different Discaria (Rhamnaceae) host species growing in patagonia.

Authors:  Eugenia E Chaia; Claudio Valverde; Luis G Wall
Journal:  Curr Microbiol       Date:  2006-11-13       Impact factor: 2.188

8.  Genome characteristics of facultatively symbiotic Frankia sp. strains reflect host range and host plant biogeography.

Authors:  Philippe Normand; Pascal Lapierre; Louis S Tisa; Johann Peter Gogarten; Nicole Alloisio; Emilie Bagnarol; Carla A Bassi; Alison M Berry; Derek M Bickhart; Nathalie Choisne; Arnaud Couloux; Benoit Cournoyer; Stephane Cruveiller; Vincent Daubin; Nadia Demange; Maria Pilar Francino; Eugene Goltsman; Ying Huang; Olga R Kopp; Laurent Labarre; Alla Lapidus; Celine Lavire; Joelle Marechal; Michele Martinez; Juliana E Mastronunzio; Beth C Mullin; James Niemann; Pierre Pujic; Tania Rawnsley; Zoe Rouy; Chantal Schenowitz; Anita Sellstedt; Fernando Tavares; Jeffrey P Tomkins; David Vallenet; Claudio Valverde; Luis G Wall; Ying Wang; Claudine Medigue; David R Benson
Journal:  Genome Res       Date:  2006-12-06       Impact factor: 9.043

9.  Micromonospora is a normal occupant of actinorhizal nodules.

Authors:  Lorena Carro; Petar Pujic; Martha E Trujillo; Philippe Normand
Journal:  J Biosci       Date:  2013-11       Impact factor: 1.826

10.  Variation in Frankia populations of the Elaeagnus host infection group in nodules of six host plant species after inoculation with soil.

Authors:  Babur S Mirza; Allana Welsh; Ghulam Rasul; Julie P Rieder; Mark W Paschke; Dittmar Hahn
Journal:  Microb Ecol       Date:  2009-03-31       Impact factor: 4.552

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