This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rouvier, C.
Right arrow Articles by Simonet, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rouvier, C.
Right arrow Articles by Simonet, P.
Agricola
Right arrow Articles by Rouvier, C.
Right arrow Articles by Simonet, P.

 Previous Article  |  Next Article 

Appl. Environ. Microbiol., 03 1996, 979-985, Vol 62, No. 3
Copyright © 1996, American Society for Microbiology

Genetic diversity among Frankia strains nodulating members of the family Casuarinaceae in Australia revealed by PCR and restriction fragment length polymorphism analysis with crushed root nodules

C Rouvier, Y Prin, P Reddell, P Normand and P Simonet
Laboratoire d'Ecologie Microbienne du Sol, Villeurbanne, France.

DNA extracted directly from nodules was used to assess the genetic diversity of Frankia strains symbiotically associated with two species of the genus Casuarina and two of the genus Allocasuarina naturally occurring in northeastern Australia. DNA from field-collected nodules or extracted from reference cultures of Casuarina-infective Frankia strains was used as the template in PCRs with primers targeting two DNA regions, one in the ribosomal operon and the other in the nif operon. PCR products were then analyzed by using a set of restriction endonucleases. Five distinct genetic groups were recognized on the basis of these restriction patterns. These groups were consistently associated with the host species from which the nodules originated. All isolated reference strains had similar patterns and were assigned to group 1 along with six of the eight unisolated Frankia strains from Casuarina equisetifolia in Australia. Group 2 consisted of two unisolated Frankia strains from C. equisetifolia, whereas groups 3 to 5 comprised all unisolated strains from Casuarina cunninghamiana, Allocasuarina torulosa, and Allocasuarina littoralis, respectively. These results demonstrate that, contrary to the results of previous molecular studies of isolated strains, there is genetic diversity among Frankia strains that infect members of the family Casuarinacaeae. The apparent high homogeneity of Frankia strains in these previous studies probably relates to the single host species from which the strains were obtained and the origin of these strains from areas outside the natural geographic range of members of the family Casuarinaceae, where genetic diversity could be lower than in Australia.


This article has been cited by other articles:

  • Huguet, V., Batzli, J. M., Zimpfer, J. F., Normand, P., Dawson, J. O., Fernandez, M. P. (2001). Diversity and Specificity of Frankia Strains in Nodules of Sympatric Myrica gale, Alnus incana, and Shepherdia canadensis Determined by rrs Gene Polymorphism. Appl. Environ. Microbiol. 67: 2116-2122 [Abstract] [Full Text]  
  • Grundmann, G. L., Normand, P. (2000). Microscale Diversity of the Genus Nitrobacter in Soil on the Basis of Analysis of Genes Encoding rRNA. Appl. Environ. Microbiol. 66: 4543-4546 [Abstract] [Full Text]  
  • Ritchie, N. J., Myrold, D. D. (1999). Geographic Distribution and Genetic Diversity of Ceanothus-Infective Frankia Strains. Appl. Environ. Microbiol. 65: 1378-1383 [Abstract] [Full Text]