Validation of a new catalysed reporter deposition–fluorescence *in situ* hybridization probe for the accurate quantification of marine *Bacteroidetes* populations

Validation of a new catalysed reporter deposition–fluorescence in situ hybridization probe for the accurate quantification of marine Bacteroidetes populations

Silvia G. Acinas, Isabel Ferrera, Hugo Sarmento, Cristina Díez-Vives, Irene Forn, Clara Ruiz-González, Fran Cornejo-Castillo, Guillem Salazar, Josep M. Gasol

2015, 17, 3557--3569.

Abstract

Catalysed reporter deposition–fluorescence in situ hybridization (CARD-FISH) is a powerful approach to quantify bacterial taxa. In this study, we compare the performance of the widely used Bacteroidetes CF319a probe with the new CF968 probe. In silico analyses and tests with isolates demonstrate that CF319a hybridizes with non-Bacteroidetes sequences from the Rhodobacteraceae and Alteromonadaceae families. We test the probes’ accuracy in 37 globally distributed marine samples and over two consecutive years at the Blanes Bay Microbial Observatory (NW Mediterranean). We also compared the CARD-FISH data with the Bacteroidetes 16S rRNA gene sequences retrieved from 27 marine metagenomes from the TARA Oceans expedition. We find no significant differences in abundances between both approaches, although CF319a targeted some unspecific sequences and both probes displayed different abundances of specific Bacteroidetes phylotypes. Our results demonstrate that quantitative estimations by using both probes are significantly different in certain oceanographic regions (Mediterranean Sea, Red Sea and Arabian Sea) and that CF968 shows seasonality within marine Bacteroidetes, notably large differences between summer and winter that is overlooked by CF319a. We propose CF968 as an alternative to CF319a for targeting the whole Bacteroidetes phylum since it has better coverage, greater specificity and overall better quantifies marine Bacteroidetes.