SSU rDNA Sequencing and PCR-Fingerprinting Reveal Genetic Variation within Glomus mosseae

Mycologia ◽  
1998 ◽  
Vol 90 (5) ◽  
pp. 791 ◽  
Author(s):  
Philippe Vandenkoornhuyse ◽  
Corinne Leyval
Mycologia ◽  
1998 ◽  
Vol 90 (5) ◽  
pp. 791-797 ◽  
Author(s):  
Philippe Vandenkoornhuyse ◽  
Corinne Leyval

Protist ◽  
2004 ◽  
Vol 155 (2) ◽  
pp. 193-214 ◽  
Author(s):  
Laure Guillou ◽  
Wenche Eikrem ◽  
Marie-Josèphe Chrétiennot-Dinet ◽  
Florence Le Gall ◽  
Ramon Massana ◽  
...  

1998 ◽  
Vol 64 (10) ◽  
pp. 3584-3590 ◽  
Author(s):  
Alenka Prinčič ◽  
Ivan Mahne ◽  
France Megušar ◽  
Eldor A. Paul ◽  
James M. Tiedje

ABSTRACT Shifts in nitrifying community structure and function in response to different ammonium concentrations (50, 500, 1,000, and 3,000 mg of N liter−1), pH values (pH 6.0, 7.0, and 8.2), and oxygen concentrations (1, 7, and 21%) were studied in experimental reactors inoculated with nitrifying bacteria from a wastewater treatment plant. The abilities of the communities selected for these conditions to regain their original structures after conditions were returned to the original conditions were also determined. Changes in nitrifying community structure were determined by performing an amplified ribosomal DNA (rDNA) restriction analysis of PCR products obtained with ammonia oxidizer-specific rDNA primers, by phylogenetic probing, by small-subunit (SSU) rDNA sequencing, and by performing a cellular fatty acid analysis. Digestion of ammonia-oxidizer SSU rDNA with five restriction enzymes showed that a high ammonium level resulted in a great community structure change that was reversible once the ammonium concentration was returned to its original level. The smaller changes in community structure brought about by the two pH extremes, however, were irreversible. Sequence analysis revealed that the highest ammonium environment stimulated growth of a nitrifier strain that exhibited 92.6% similarity in a partial SSU rRNA sequence to its nearest relative, Nitrosomonas eutropha C-91, although the PCR product did not hybridize with a general phylogenetic probe for ammonia oxidizers belonging to the β subgroup of the classProteobacteria. A principal-component analysis of fatty acid methyl ester data detected changes from the starter culture in all communities under the new selective conditions, but after the standard conditions were restored, all communities produced the original fatty acid profiles.


2018 ◽  
Vol 128 (1) ◽  
pp. 37-49 ◽  
Author(s):  
J Naldoni ◽  
AAM Maia ◽  
LL Correa ◽  
MRM Silva ◽  
EA Adriano
Keyword(s):  
Ssu Rdna ◽  

Zootaxa ◽  
2019 ◽  
Vol 4664 (2) ◽  
pp. 206-220
Author(s):  
CONGCONG WANG ◽  
ZHISHUAI QU ◽  
XIAOZHONG HU

Four cyrtophorian ciliates, Chlamydodon pararoseus sp. n., Chlamydodon bourlandi Qu et al., 2018, Dysteria crassipes Claparède & Lachmann, 1859, and Dysteria monostyla (Ehrenberg, 1838) Kahl, 1931, isolated from coastal waters off China, were investigated using morphological and SSU rDNA sequencing techniques. C. pararoseus sp. n. can be recognized by having a kidney-shaped body, a complete cross-striated band, 44–51 somatic kineties, and 11–14 nematodesmal rods. The other three species were re-described based on new populations. Additionally, the SSU rRNA genes of C. pararoseus sp. n. and D. monostyla were sequenced for the first time. Phylogenetic analyses inferred from SSU rRNA gene sequences reveal that C. pararoseus sp. n. has a close relationship with C. bourlandi and C. mnemosyne Gong et al., 2005 within the genus Chlamydodon; and D. monostyla and D. crassipes cluster with its congeners, which confirms their generic assignments. 


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