Molecular detection and phylogenetic analysis of Mycoplasma bovis in cattle in Nineveh governorate, Iraq
Khoder A. Al-Azow,
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Qaes T. Alsarhan,
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Mohammad A. Hamad
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et al.
Al-mağallaẗ al-ʻirāqiyyaẗ li-l-ʻulūm al-bayṭariyyaẗ/Iraqi journal of veterinary sciences,
Journal Year:
2024,
Volume and Issue:
38(3), P. 615 - 622
Published: June 30, 2024
This
study
targeted
to
determine
the
prevalence
of
Mycoplasma
bovis
in
cattle
Nineveh
Governorate,
Iraq,
based
on
three
genes,
including
16S
rRNA,
uvrC,
and
gapA
using
polymerase
chain
reaction
(PCR)
techniques,
investigate
phylogenetic
analysis
M.
diagnose
study.
Various
samples,
352
blood
nasal
swabs,
40
ocular
65
synovial
fluid,
30
milk
were
randomly
obtained
from
cattle.
Based
amplified
rRNA
gene,
spp
was
38.63%
c-PCR
technique.
At
same
time,
there
no
significant
uvrC
which
30.68%
28.69%,
respectively,
m-PCR
No
difference
found
between
types
samples
for
detecting
bovis.
The
ten
local
sequences
(5
sequence)
that
deposited
NCBI
GenBank
under
accession
numbers
OR784598.1-OR784602.1
OR792211.1-OR792215.1,
with
highly
related
99.13-100%
identity
99.81%
identity,
other
registered
different
countries,
Canada,
Egypt,
Iran,
Poland,
Switzerland.
concludes
is
widespread
Iraq.
first
highlights
Language: Английский
Prevalence of Mycoplasma bovis in Cattle in Nineveh Governorate, Iraq
Khoder A. Al-Azow,
No information about this author
Qaes T. Alsarhan,
No information about this author
Mohammad A. Hamad
No information about this author
et al.
Egyptian Journal of Veterinary Science,
Journal Year:
2024,
Volume and Issue:
56(4), P. 0 - 0
Published: May 25, 2024
The
current
study
aimed
to
determine
the
prevalence
of
Mycoplasma
bovis
in
cattle
Nineveh
Governorate,
Iraq,
using
culture
method,
indirect
enzyme-linked
immunosorbent
assay
(i-ELISA),
and
conventional
polymerase
chain
reaction
(c-PCR)
technique,
evaluate
efficiency
various
laboratory
methods
used
this
study.
During
period
from
March
2022
February
2023,
a
total
352
nasal
swabs
were
collected
randomly
tested
method
technique
(amplifying
uvrC
gene)
for
isolation
molecular
detection
M.
,
respectively.
Moreover,
blood
samples
same
animals
antibodies
against
i-ELISA.
results
observed
that
was
23.57%
(83
out
352)
30.68%
(108
c-PCR
47.15%
(166
According
Kappa
value
(0.807),
there
perfect
agreement
between
with
sensitivity,
specificity,
accuracy
98.79%,
90.33%,
92.32%
While
moderate
i-ELISA
test
based
on
(0.444),
specificity
89.15%,
65.79%,
71.30%
i-ELISA,
This
concluded
is
prevalent
Governorate
PCR
more
efficient
tool
than
ELISA
suspected
samples.
Language: Английский
Analysis of Coinfection Pathogens From Foot‐and‐Mouth Disease Virus Persistently Infected Cattle Using Oxford Nanopore Sequencing
Shuang Wang,
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Sumin Wei,
No information about this author
Yaozhong Ding
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et al.
Transboundary and Emerging Diseases,
Journal Year:
2024,
Volume and Issue:
2024(1)
Published: Jan. 1, 2024
The
persistent
infection
caused
by
foot‐and‐mouth
disease
virus
(FMDV)
still
lacks
a
reliable
explanation,
as
its
etiology
and
maintenance
are
intricate
potentially
involve
concurrent
infections
with
multiple
pathogens.
In
this
study,
we
utilized
the
nanopore
platform
for
direct
sequencing
of
clinical
samples
obtained
from
cattle
persistently
infected
FMDV
serotype
O
investigated
distribution
characteristics
coinfecting
pathogens
in
their
pharyngeal
region.
Briefly,
exploited
Oxford
Nanopore
technology
to
generate
high‐quality
sufficient
sequence
data
comprehensive
characterization
microbial
genomes.
Furthermore,
performed
comparison,
alignment,
phylogenetic
tree
construction.
Our
findings
revealed
total
23
viruses
carrier
bovine,
FMDV,
bovine
orthopneumovirus,
Choristoneura
fumiferana
granulovirus
emerging
top
three
identified
analysis
unexpectedly
presence
porcine
circovirus
type
2
pepper
mild
mottle
among
viral
genes
detected
carrier.
Compared
noncarrier,
exhibited
greater
diversity
abundance
mycoplasma
types
well
reads
counts.
Therefore,
propose
that
establishment
perpetuation
may
be
attributed
simultaneous
other
agents
mycoplasmas.
These
highlight
significance
investigating
multipathogen
coinfection
elucidating
FMD
infection.
Language: Английский