scholarly journals TheEscherichia colicytochromeb556gene,cybA, is assignable assdhCin the succinate dehydrogenase gene cluster

1985 ◽  
Vol 30 (3) ◽  
pp. 307-311 ◽  
Author(s):  
Hiroshi Murakami ◽  
Kiyoshi Kita ◽  
Hiroshi Oya ◽  
Yasuhiro Anraku
PLoS ONE ◽  
2019 ◽  
Vol 14 (6) ◽  
pp. e0218569 ◽  
Author(s):  
Tamieka Lee Pearce ◽  
Calum Rae Wilson ◽  
David Hugh Gent ◽  
Jason Barry Scott

Plant Disease ◽  
2014 ◽  
Vol 98 (4) ◽  
pp. 532-539 ◽  
Author(s):  
Achour Amiri ◽  
Stacy M. Heath ◽  
Natalia A. Peres

Succinate dehydrogenase inhibitors (SDHIs) constitute a mainstay in management of gray mold caused by Botrytis cinerea in strawberry and several other crops. In this study, we investigated the risks of resistance development to three newer SDHIs (i.e., fluopyram, fluxapyroxad, and penthiopyrad) and their cross-resistance with the previously registered boscalid. We investigated the mutations in the SdhB subunit and evaluated their impact on microbial fitness in field populations of B. cinerea. Amino acid substitutions associated with resistance to SDHIs were detected at three codons of the SdhB subunit (BH272R/Y/L, BP225F, and BN230I) in the succinate dehydrogenase gene of field isolates from Florida. The BH272R, BH272Y, BH272L, BP225F, and BN230I mutations were detected at frequencies of 51.5, 28.0, 0.5, 2.5, and 4%, respectively. Strong cross-resistance patterns were evident between boscalid and fluxapyroxad and penthiopyrad but not with fluopyram, except in BH272L, BP225F, and BN230I mutants. All five mutations conferred moderate to very high resistance to boscalid whereas the BH272Y conferred resistance to fluxapyroxad and penthiopyrad. The BH272L, BN230I, and BP225F mutations conferred high resistance to all four SDHIs tested. Resistance monitoring following the first use of penthiopyrad in strawberry fields in Florida in 2013 suggests potential for quick selection for highly resistant populations and warrants careful use of the newer SDHIs. No evidence of major fitness costs due to the mutations in the SdhB subunit was found, which indicates the potential ability of the mutants to survive and compete with wild-type isolates. Our study suggests high risks for rapid widespread occurrence of B. cinerea populations resistant to the novel SDHIs unless appropriate rotation strategies are implemented immediately upon registration.


Heliyon ◽  
2020 ◽  
Vol 6 (11) ◽  
pp. e05387
Author(s):  
Adriana Higuera ◽  
Marina Muñoz ◽  
Myriam Consuelo López ◽  
Patricia Reyes ◽  
Plutarco Urbano ◽  
...  

2008 ◽  
Vol 123 (1) ◽  
pp. 141-144 ◽  
Author(s):  
R Garrel ◽  
P Raynaud ◽  
I Raingeard ◽  
C Muyshondt ◽  
Q Gardiner ◽  
...  

AbstractObjective:To report a rare case of a laryngeal paraganglioma related to succinate dehydrogenase gene mutation C.Method:A case report and a review of the world literature concerning succinate dehydrogenase mutations and laryngeal paraganglioma are presented.Results:We identified a laryngeal paraganglioma in a 38-year-old woman, related to a very rare, deleterious in exon 4 of the succinate dehydrogenase mutation C. This mutation was a non-sense mutation: c.183G >A leading to p.Trp61X. No other neuroendocrine tumour was identified in this case, but a thyroid papillary carcinoma was concomitantly discovered and cured.Conclusion:To our knowledge, this is the first report in the world literature of laryngeal paraganglioma related to a succinate dehydrogenase mutation C. The case presented underlines the fact that every patient with paraganglioma should be tested for succinate dehydrogenase genetic mutations, even if a family history of paraganglioma is absent, in order to enable appropriate clinical management and to improve our knowledge of familial paraganglioma.


Gene ◽  
2008 ◽  
Vol 414 (1-2) ◽  
pp. 41-48 ◽  
Author(s):  
Robert F. Massung ◽  
Shannon L. Hiratzka ◽  
Kelly A. Brayton ◽  
Guy H. Palmer ◽  
Kemba N. Lee

2013 ◽  
Vol 170 (15) ◽  
pp. 1349-1352 ◽  
Author(s):  
Alexander T. Eprintsev ◽  
Dmitry N. Fedorin ◽  
Abir U. Igamberdiev

2003 ◽  
Vol 185 (8) ◽  
pp. 2548-2554 ◽  
Author(s):  
Gwendolyn E. Wood ◽  
Andrew K. Haydock ◽  
John A. Leigh

ABSTRACT Methanococcus maripaludis is a mesophilic species of Archaea capable of producing methane from two substrates: hydrogen plus carbon dioxide and formate. To study the latter, we identified the formate dehydrogenase genes of M. maripaludis and found that the genome contains two gene clusters important for formate utilization. Phylogenetic analysis suggested that the two formate dehydrogenase gene sets arose from duplication events within the methanococcal lineage. The first gene cluster encodes homologs of formate dehydrogenase α (FdhA) and β (FdhB) subunits and a putative formate transporter (FdhC) as well as a carbonic anhydrase analog. The second gene cluster encodes only FdhA and FdhB homologs. Mutants lacking either fdhA gene exhibited a partial growth defect on formate, whereas a double mutant was completely unable to grow on formate as a sole methanogenic substrate. Investigation of fdh gene expression revealed that transcription of both gene clusters is controlled by the presence of H2 and not by the presence of formate.


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