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Cypriniformes (Table 6.2). Hagi
et al
. (2004) investigated the composition of intestinal LAB
in silver carp (
Hypophthalmichthys molitrix
) in Lake Kasumigaura during different seasons.
As was observed for the common carp and deep-bodied crucian carp, the LAB levels in the GI
tract were higher during the summer (27
∘
C) than in the winter (9.8
∘
C). However, this differ-
ence was more subtle in the silver carp (LAB levels were log 5 CFU g
−1
during the summer
and winter) compared to the common carp and deep-bodied crucian carp (LAB levels were
log 6 and log 7 CFU g
−1
in the summer, respectively, and log 5 CFU g
−1
in the winter). The
proportion of LAB with respect to the total culturable populations was less than 1% in silver
carp at both sampling points. The authors reported that the predominant intestinal LAB of all
carp species was
Lc. lactis
in the summer and
Lc. raffinolactis,
in the winter. Ghiasi (2011)
also reported the presence of
Lc. raffinolactis,
and
Lc. lactis
as allochthonous intestinal LAB
in silver carp as well as
Lb. plantarum
.
In an early study Halami
et al
. (1999) isolated and characterized
Pediococcus
sp. and
P.
acidilactici
from the gut of rohu (
Labeo rohita
). These bacteria were tested for antibacte-
rial production against several different pathogenic LAB, but they did not belong to the most
promising LAB tested, which were isolated from fowl and mushroom.
In a recent study Wu
et al
. (2012a) used a next-generation sequencing approach to investi-
gate the intestinal microbial community of grass carp (
Ctenopharyngodon idellus
). A complex
microbial community was revealed and the community was rich in cellulose-degrading bacte-
ria such as
Anoxybacillus
,
Leuconostoc
,
Clostridium
,
Actinomyces
and
Citrobacter
typical of
herbivorous species. In addition, 1.61%-7.65% of the communities were identified as
Lacto-
bacillus
spp. and 1.59% as
Streptococcus
spp.
The zebrafish (
Danio rerio
) model has been introduced in a wide variety of research fields
including studies to elucidate the importance of the gut microbiota in relation to health and
disease of vertebrates.
Lb. fermentum
,
Lc
.
lactis
subsp.
cremoris
,
Lc
.
lactis
subsp.
lactis
,
Lc
.
lactis
,
Lc
.
piscum
,
Lc
.
plantarum
,
Lc
.
raffinolactis,
,
Leu
.
citreum
and
Str. thermophilus
have
been identified as constituents of the gut microbiome of zebrafish (Rawls
et al
. 2004; Gioac-
chini
et al
. 2012). Further studies have reported that a wide range of LAB species, particularly
lactobacilli, display favourable characteristics for zebrafish intestinal colonization and mucosal
adhesion (Gioacchini
et al
. 2012; Zhou
et al
. 2012).
6.13 CHANNIDAE
The snakeheads are members of the freshwater perciform fish family Channidae. Allameh
(2012) reported that
Ae. viridans
,
Lb. delbrueckii
subsp.
delbrueckii
and
E. faecalis
were com-
mon in the stomach and intestine of snakehead juveniles (
Channa striatus
Bloch 1793) while
strains belonging to
Lb
.
fermentum
and
Leu
.
mesenteroides
subsp.
mesenteroides
were detected
in the stomach and intestine of adult fish. Antagonistic activities tested against
A
.
hydrophila
,
Pseudomonas aeruginosa
and
Shewanella putrefaciens
indicated that
E. faecalis
,
Lb
.
fermen-
tum
and
Leu
.
mesenteroides
subsp.
mesenteroides
displayed highest
in vitro
inhibition against
the pathogenic bacteria (Allameh 2012; Allameh
et al
. 2012). More recently, Allameh
et al
.
(2013) isolated
Lb
.
fermentum
from the stomach of snakeheads.
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