Skip to main content
Publications | Persons | Institutes | Projects
[ report an error in this record ]basket (0): add | show Print this page

Erythromycin and GC7 fail as domain-specific inhibitors for bacterial and archaeal activity in the open ocean
Frank, A.H.; Pontiller, B.; Herndl, G.; Reinthaler, T. (2016). Erythromycin and GC7 fail as domain-specific inhibitors for bacterial and archaeal activity in the open ocean . Aquat. Microb. Ecol. 77: 99-110. dx.doi.org/10.3354/ame01792
In: Aquatic Microbial Ecology. Inter-Research: Oldendorf/Luhe. ISSN 0948-3055; e-ISSN 1616-1564, more
Peer reviewed article  

Available in  Authors 

Author keywords
    N1-guanyl-1,7-diaminoheptane; Secondary production; Prokaryotes; MICROCARD-FISH; Dark ocean; Antibiotics; North Atlantic Ocean; Microautoradiography

Authors  Top 
  • Frank, A.H.
  • Pontiller, B.
  • Herndl, G., more
  • Reinthaler, T.

Abstract
    Domain-specific metabolic inhibitors are currently used to differentiate archaealfrom bacterial activity. However, studies testing the specificity of these inhibitors are sparse or arebased on cultured strains. We determined the inhibition specificity of erythromycin (EMY) andN1-guanyl-1,7-diaminoheptane (GC7) on bacterial and archaeal communities in the NorthAtlantic. EMY and GC7 are assumed to inhibit bacterial and archaeal activity, respectively. Heterotrophicprokaryotic activity was estimated via 3H-leucine incorporation on the cell-specificlevel using catalyzed reporter deposition fluorescence in situ hybridization combined withmicroautoradiography (MICRO-CARD-FISH). In the water masses studied, the contribution ofThaumarchaeota to total picoplankton abundance ranged from 5 to 24% while Euryarchaeotacontributed 2 to 6%; the relative abundance of Bacteria ranged from 29 to 48%. The addition ofEMY and GC7 reduced the bulk leucine incorporation by ~77% and ~41%, respectively. Evaluationof the inhibition efficiency of EMY on a cell-specific level showed no difference betweenArchaea (76.0 ± 14.2% [SD]) and Bacteria (78.2 ± 9.5%). Similarly, the reduction of substrateuptake in GC7-treated samples was similar in Archaea (59.9 ± 24%) and Bacteria (47.2 ± 9.6%).Taken together, our results suggest that in complex open-ocean prokaryotic communities neitherEMY nor GC7 is efficient as a domain-specific inhibitor.

All data in the Integrated Marine Information System (IMIS) is subject to the VLIZ privacy policy Top | Authors