investigated so far, but its nab gene cluster appears similar to that of Vibrio vulnificus CMCP6, which produces the alanyl carrying Leg variant Leg5Ac7AcAla 39. The diversity of nab clusters within Vibrionaceae has already been shown, with an emphasis on Vibrio vulnificus 28. The distribution of NulOs in Moritellaceae has not been studied. This study investigates the presence and composition of nab gene clusters in a set of strains from A. salmonicida (Vibrionaceae) and M. viscosa (Moritellaceae), as well as A. wodanis and a few other members of the Vibrionaceae family. The strains were previously isolated from different kinds of organisms such as fish, sponge and amphipod (for a summary of the strains used in this study, see Table 1 in the Materials and Methods section). They were screened for the presence of NeuB sequences, which were then used to locate nab clusters in their genomes as well as investigate the sequence determinants of NeuB substrate specificity. Each cluster was analyzed in terms of gene content and organization, using sequence homology as a basis for functional annotation. From this, hypotheses pertaining to the nature of the NulO(s) produced by each strain could be made, and a set of candidates for experimental analysis was obtained. The NulO content of a few strains was analyzed using mass spectrometry in order to obtain preliminary experimental results. Results and discussion comparison of neuB sequences. Sequence alignment and phylogeny. NeuB protein sequences from A. salmonicida LFI1238, M. viscosa 06/09/139 and A. wodanis were used as queries for conducting a sequence similarity search within the set of target genomes (see Table 1). Out of the 15 targets, 10 had at least one sequence identical to one of the queries, and 3 had a similar sequence. As expected, no NeuB coding sequences were found in either P. phosphoreum or V. anguillarum. A fingerprint of the alignment of unique NeuB sequences and NeuB phylogeny are presented in Fig. 2 (the full alignment is included as Supplementary Information, in Figure S1). Six of the eight targeted M. viscosa strains have two NeuB coding sequences identical to the ones from the 06/09/139 strain. The two remaining strains contain each one sequence, identical to either the Neu-pathway homolog (strain F57) or the Pse-pathway homolog (strain NVI-5482). This is consistent with the evolutionary relations between M. viscosa genomes according to which those two strains form their own clade 40. It is also interesting to note that the strains with identical sequences were isolated from either salmond or rainbow trout, while the NVI-5482 and F57 were obtained from cod and lumpfish, respectively. For the Aliivibrio strains, two strains (A. salmonicida R8-68 and R8-70, isolated from the amphipod Eurythenes gryllus) have sequences