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(oesophagus, stomach, PI and DI) in beluga and Persian sturgeon. Mean LAB levels in beluga
and Persian sturgeons were 7.9 × 10
6
CFU g
−1
and 5.4 × 10
6
CFU g
−1
, respectively. Maximum
LAB levels were reported in the DI of beluga (3.8 × 10
6
CFU g
−1
) and Persian sturgeon (4.6
× 10
6
CFU g
−1
) while minimum levels were present in the PI (3.2 × 10
5
CFU g
−1
in beluga
and 1.1 × 10
5
CFU g
−1
in Persian sturgeon). 16S rRNA partial sequencing of LAB isolates
(
n
= 70) from beluga and Persian sturgeon revealed that 25 isolates were identified (98-99%
sequence alignment) as
Lb. curvatus
, eight isolates as
Lactococcus raffinolactis,
, five isolates
as
Lc. lactis
spp.
cremoris
, and two isolates as
Streptococcus
spp. Furthermore, in Persian
sturgeon 22 isolates were identified as
Leu
.
mesenteroides
and eight isolates as
Enterococcus
seriolicida
. Based on these results, the authors concluded that the DI is the best region for
isolating LAB in the GI tract of beluga and Persian sturgeon and that the LAB community
composition differed between the species (Askarian
et al
. 2009). It was interesting to note
therefore that, in a later study, Askarian
et al
. (2011) observed that dietary administration of
Lb
.
curvatus
(isolated by Askarian
et al
. 2009) improved the growth performance and diges-
tive enzyme activities of beluga whereas the application of
Leu
.
mesenteroides
(isolated by
Askarian
et al
. 2009) did not. In contrast, in Siberian sturgeon
Leu
.
mesenteroides
applica-
tion improved the growth performance and digestive enzyme activities but
Lb
.
curvatus
did
not. These studies would infer that the dominant LAB communities in these sturgeon species
display host specificity and that they might have important influences on the host.
Ghanbari
et al
. (2009) isolated and characterized LAB from intestine of beluga and Persian
sturgeons inhabiting the Caspian Sea using culture based techniques followed by biochem-
ical tests. Their results showed relatively high levels of LAB in the intestine of beluga (log
5.3 CFU g
−1
) and Persian sturgeon (log 6.4 CFU g
−1
). Biochemical tests of the gut isolates
indicated prevalence of
Lb. sakei
,
Lb. plantarum
,
Lb. alimentarius
,
Lb. casei
in beluga and
Lb.
sakei
and
Lb. brevis
in Persian sturgeon. In a more recent study, Soltani
et al
. (2013) reported
that culturable autochthonous LAB ranged from log 2.93 to 5.61 CFU g
−1
intestine in Persian
sturgeon. 16S rRNA gene sequence analysis revealed that the LAB community was dominated
by
Lc
.
garvieae
and
Lc
.
lactis
. In addition the authors reported that
Pediococcus pentosaceus
,
W
.
cibaria
and
E. faecalis
were minor components of the LAB community.
Characterization of indigenous microbiota, especially LAB, using culture-independent
molecular approaches like PCR-DGGE, next-generation sequencing and FISH, which provide
a more comprehensive assessment of bacterial communities, has so far been neglected in stur-
geon studies. Thus, determination of indigenous LAB and their levels in different life stages
of sturgeon species, for the development of optimum prebiotic and probiotic applications, is
an obvious topic for future research.
6.8 PERCIDAE AND SCIAENIDAE
It has been demonstrated that LAB species are members of the
normal
microbiota of some Per-
cidae (Bucio
et al
. 2006) and Sciaenidae (Sica
et al
. 2010).
Lb. coryneformis
subsp
. torquens
,
Lb.sakei
,
Biidobacteriumdentium
and lactobacilli have been isolated from perch (
Percaluvi-
atilis
) (Bucio
et al
. 2006; Vlková
et al
. 2012),
Lactobacillus
spp. from ruffe (
Gymnocephalus
cernuus
) (Bucio
etal
. 2006),
W
.
viridescens
and
Leu.mesenteroides
subsp
.mesenteroides
from
stripped weakfish (
Cynoscion guatucupa
) (Sica
et al
. 2010) and
Leu. mesenteroides
subsp
.
mesenteroides
from
Micropogonias furnieri
(Sica
et al
. 2010).
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