2024-03-29T17:55:04Z
https://ijvr.shirazu.ac.ir/?_action=export&rf=summon&issue=711
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
FSH and eCG impact follicles development and expression of ovarian FSHR and caspase-9 in mice
S.
Wei
Z.
Gong
H.
Guo
T.
Zhang
Z.
Ma
The study aimed to investigate the effects of FSH and eCG on the ovarian and follicular development, expression levels of FSHR and caspase-9 of ovaries in vivo. One hundred and five prepuberty mice were allocated into FSH-1, FSH-2, FSH-3, eCG-1, eCG-2, eCG-3 groups and control group (CG). Mice in FSH-1, FSH-2 and FSH-3 were intramuscularly injected with 5, 10 and 20 IU FSH twice (on day 0 and 4), respectively. Mice in eCG-1, eCG-2 and eCG-3 were intraperitoneally injected with 10, 20 and 40 IU eCG on day 0 and 4. Mice in the CG were injected with 0.5 ml normal saline on day 0 and 4. Left and right ovaries of each mouse were dissected aseptically on days 7, 14 and 21, respectively. The results showed that on days 14 and 21 the ovarian sizes and follicle numbers of FSH-3 and eCG-3 groups were greater than CG (P<0.05). FSHR mRNA of FSH-2 and eCG-1 were higher than CG on days 14 and 21 (P<0.05). FSHR proteins of FSH-3 were higher than CG on days 14 and 21 (P<0.05). Caspase-9 mRNA in FSH and eCG groups was less than CG. There were positive correlations between follicle numbers and FSH and eCG doses. FSHR protein expressions had positive correlations between ovarian weights and sizes of ovary and follicle numbers (r=0.971, P<0.05) in FSH-treated mice. Serum FSH concentrations of FSH-2, FSH-3, eCG-2 and eCG-3 groups were greater than that of CG. In conclusion, eCG and FSH promoted the ovarian development, follicle genesis, FSH secretion, FSHR mRNA and protein expressions in ovaries of mice. FSH and eCG inhibited the expression of ovarian caspase-9 mRNA.
Caspase-9
Equine chorionic gonadotrophin
Follicle stimulating hormone receptor
Gene expression
Ovarian development
2017
06
01
79
85
https://ijvr.shirazu.ac.ir/article_4085_6f53bc3cba0bf8c23f8a6bb08aea573d.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
Evaluation of the timing of the Escherichia coli co-infection on pathogenecity of H9N2 avian influenza virus in broiler chickens
N.
Mosleh
H.
Dadras
K.
Asasi
M. J.
Taebipour
S. S.
Tohidifar
Gh.
Farjanikish
Bacterial co-infections can probably influence the pathogenicity of H9N2 low pathogenic avian influenza virus (AIV). This study aimed to evaluate the effect of exposure time to Escherichia coli (O:2) on the pathogenicity of H9N2 AIV in broiler chickens. Three hundred and sixty broiler chickens were randomly allocated to six equal groups. At the age of 26 days, all chicks except groups 5 and 6 were inoculated intra-nasally with H9N2 virus. At the same time, the birds in groups 1 and 5 were infected with E. coli via spray route. Birds in groups 3 and 2 were infected with E. coli three days prior to and three days post AI challenge, respectively. Mortality rates, clinical signs, gross and microscopic lesions, excretion and duration of virus shedding in faecal and tracheal samples and seroconversion to H9N2 virus were assessed in the challenged groups. The highest mortality rate was observed in chickens inoculated with H9N2 followed by E. coli. The most severe clinical signs, gross lesions, mortality rate and virus detection were observed at day 6 post challenge (PC) in birds of group 2, while the duration of virus shedding was longer in group 3 (E. coli followed by H9N2) than other groups. In conclusion, E. coli infection prior to, after or concurrently with H9N2 virus infection could exacerbate the adverse effects of the virus. Our results indicate that E. coli and H9N2 together can mutually exacerbate the condition of either disease in broiler chicks as compared to single infected birds.
Avian influenza virus
Escherichia coli
Exposure time
H9N2
Pathogenesis
2017
06
01
86
91
https://ijvr.shirazu.ac.ir/article_4086_efc33783db5638e020f69c347a30aa56.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
Detection of specific antigens of Newcastle disease virus using an absorbed Western blotting method
F.
Hemmatzadeh
M.
Kazemimanesh
Newcastle disease virus (NDV) is an economically important poultry pathogen with a worldwide distribution that may infect a wide range of domestic and wild avian species. The identification of different pathotypes of NDVs plays an important role in the diagnosis and development of vaccines to control and eradicate NDV infections. In our previous study, we showed that mono-specific antibodies can differentiate velogenic and lentogenic strains of NDV in Agar Gel Immuno-Diffusion tests. To evaluate the ability of the specific antibodies to detect NDV specific antigens, this study was conducted with a range of NDV isolates. The samples included 9 NDV neuropathogenic/velogenic isolates from diseased chickens collected from poultry farms in central and northern parts of Iran plus La-Sota and B1 vaccine strains. All samples were propagated in embryonated chicken eggs and concentrated and purified by ultra-centrifugation. All samples were subjected to 12.5% SDS-PAGE and Western blotting using the specific antibodies mentioned previously. In SDS-PAGE all velogenic and vaccine strains showed the same electrophoretic pattern. The detected bands included 15, 38, 46, 48, 53, 55, 68, 74 and 220 kDa proteins. In Western blotting analysis, the mono-specific antibodies reacted specifically to the viral proteins with 15, 38, 48, 55, 74 and 220 kDa and non-specifically to the viral protein with 53 kDa. The results suggest that specific anti-NDV antibodies can react specifically to glycoproteins (haemagglutin-neuraminidase and fusion proteins) but not to internal proteins (nucleoprotein or matrix protein) of NDV strains.
Newcastle disease virus
Specific antigens
Western blotting method
2017
06
01
92
96
https://ijvr.shirazu.ac.ir/article_4087_667a17914253a91458ffd459394cda0b.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
VacA and cagA genotypes status and antimicrobial resistance properties of Helicobacter pylori strains isolated from meat products in Isfahan province, Iran
A.
Gilani
V.
Razavilar
N.
Rokni
E.
Rahimi
Although Helicobacter pylori has a significant impact on the occurrence of severe clinical syndromes, its exact ways of transmission and origin have not been identified. According to the results of some previously published articles, foods with animal origins play a substantial role in the transmission of H. pylori to humans. The present investigation was carried out to study the vacuolating cytotoxin A (vacA) and cytotoxin associated gene A (cagA) genotypes status and antibiotic resistance properties of H. pylori strains recovered from minced-meat and hamburger samples. A total of 150 meat product samples were collected from supermarkets. All samples were cultured and the susceptive colonies were then subjected to nested-PCR, PCR-based genotyping and disk diffusion methods. 11 out of 150 samples (7.33%) were positive for H. pylori. All the isolates were further identified using the nested-PCR assay. Prevalence of H. pylori in hamburger and minced-meat samples was 1.42% and 12.5%, respectively. S1a, m1a and cagA were the most commonly detected genotypes. The most commonly detected combined genotypes in the H. pylori strains of minced-meat were s1am1a (10%), s1am1b (10%) and s2m1a (10%). Helicobacter pylori strains of meat products harbored the highest levels of resistance against ampicillin (90.90%), erythromycin (72.72%), amoxicillin (72.72%), trimethoprim (63.63%), tetracycline (63.63%), and clarithromycin (63.63%). Hamburger and minced-meat samples may be the sources of virulent and resistant strains of H. pylori. Meat products are possible sources of resistant and virulent strains of H. pylori similar to those vacA and cagA genotypes. Using healthy raw materials and observation of personal hygiene can reduce the risk of H. pylori in meat products.
Antibiotic resistance pattern
cagA
Helicobacter pylori
Meat products
vacA
2017
06
01
97
102
https://ijvr.shirazu.ac.ir/article_4088_e5f6c2166ba2e03f48af7b7bdbf31984.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
Efficacy of thermostable I-2 Newcastle disease vaccine compared to B1 commercial vaccine in broiler chicken
A. H.
Asl Najjari
H.
Nili
K.
Asasi
N.
Mosleh
H.
Rohollahzadeh
S.
Mokhayeri
Frequent vaccination failures have occurred in the broiler farms in Eurasian countries during Newcastle disease outbreaks. The disease is enzootic in many countries of the region, especially in southwest Asia. I-2 vaccine has been used successfully in village chickens in many Asian and African countries. Our preliminary study showed good efficacy of the vaccine in broiler chickens. Therefore the current experimental study was conducted to compare viral shedding period of heat resistance I-2 vaccine with B1 commercial vaccine following challenge with Herts’33. For this purpose three hundred commercial broilers were randomly allocated into four groups; 1) Thermostable I-2 vaccine, 2) Hitchner B1 vaccine, 3) Challenge group with no vaccine, and 4) Negative control group. Experimental chicks were vaccinated on days 19 and 26 by the eye drop route and then the birds were challenged via intra ocular route on day 40 with a suspension containing 106 EID50/ml challenge virus. Experimental chickens were monitored by collecting buccal and cloacal swabs at different times. Collected swabs were submitted to PCR test. The results showed that vaccination can protect the birds against mortality and also decrease virus shedding; also there was not a significant difference between vaccination with I-2 and B1 vaccines.
Broiler chicken
Hitchner B1 vaccine
Newcastle disease
Thermostable I-2 vaccine
Virus Shedding
2017
06
01
103
107
https://ijvr.shirazu.ac.ir/article_4089_900713a6a733793012e78a475c16e25f.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
The effect of intra-cerebroventricular injection of insulin on nociception of formalin test in non-diabetic and short-term diabetic rat models
Sh.
Balali Dehkordi
J.
Sajedianfard
A. A.
Owji
Pain is a complex process in the central nervous system (CNS). Several factors can alter the pain threshold and insulin is one of them which is produced by the beta cells of pancreas and capable of crossing blood-brain barrier. The aim of this study was to evaluate the effects of intra-cerebroventricular (ICV) injection of insulin on the pain response to formalin in short-term induced diabetic and non-diabetic rats. Sixty-four Sprague-Dawley male rats (280 ± 30 g) were divided into non-diabetic and diabetic groups. Diabetes was induced with streptozotocin (STZ, 60 mg/kg, i.p) for elimination of peripheral insulin. After proving diabetes, insulin (5 mU/animal, 5 μL) was injected to the left lateral cerebral ventricle while equal volume of normal saline was injected in control groups. After 10 min, formalin test was performed. Present study showed that ICV injection of insulin possessed anti-nociceptive effect in non-diabetic rats in formalin test while in diabetic rats, it did not have this effect and even decreased pain threshold partially. In conclusion we showed that ICV injection of insulin in non-diabetic rats, in contrast with diabetic rats, has an anti-nociceptive effect in formalin test. In short-term diabetic rats, ICV injection of insulin was not able to reduce pain response and partially decreased pain threshold.
Formalin test
Insulin
pain
Short-term diabetes
2017
06
01
108
112
https://ijvr.shirazu.ac.ir/article_4094_a392c57adc3f2a29825178e9c8c1b5de.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
Transfection of bovine spermatogonial stem cells in vitro
P.
Tajik
Kh.
Hoseini Pajooh
Z.
Fazle Elahi
G.
Javdani Shahedin
H.
Ghasemzadeh-Nava
Spermatogonial stem cells (SSCs) are the only stem cells in adults that can transfer genetic information to the future generations. Considering the fact that a single SSC gives rise to a vast number of spermatozoa, genetic manipulation of these cells is a potential novel technology with feasible application to various animal species. The aim of this study was to evaluate enhanced green fluorescent protein (EGFP) gene transfection into bovine SSCs via liposome carrier and assess the best incubation day in uptake exogenous gene by SSCs. Transfection efficiency of EGFP gene with lipofectamine 2000 was determined in days following each three day of transfection (day 4, 6 and 8 of the culture) by fluorescent microscope. Results showed that the transfected cells through lipofection increased significantly (P<0.05) in each three days of transfection in comparison with those of the control groups. The transfected SSCs were higher in comparison with those of the free exogenous gene carrier groups (P<0.05). In comparison with these three days, the rate of infected cells was higher when transfection proceeds at day four. It was concluded that lipofectamine can be used safely for direct loading exogenous DNA to SSCs particularly during the fourth day of culture.
EGFP
Lipofection
Spermatogonial stem cells
2017
06
01
113
118
https://ijvr.shirazu.ac.ir/article_4095_209a0c25c3fc069a9eb91415d912dc32.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
Clinical studies on progressive retinal atrophy in 31 dogs
D. N.
Kelawala
D. B.
Patil
P. V.
Parikh
M. J.
Sheth
C. G.
Joshi
B.
Reddy
During a 2-year period, 31 cases of a hereditary retinal degeneration in dogs bred in India were found mainly suspected for progressive retinal atrophy (PRA) with typical history of initial nyctalopia followed by hemeralopia. Out of 31 PRA suspected dogs, 8 dogs (26%) were from the age group of 1-5 years, 15 (48%) 6-10 years and the rest (26%) 11-15 years. The most predominant breed was Spitz (18 dogs, 58%). Detailed ophthalmologic examinations included Schirmer’s tear test, fluorescein stain, applanation tonometry, slit lamp biomicroscopy and ocular ultrasound in appropriate cases. Ophthalmoscopic and fundoscopic changes included hyperreflectivity and discoloration of the tapetal area, marked attenuation of retinal vessels, depigmentation in non-tapetal area and optic disc atrophy with scalloped borders. Electroretinograms (ERG) recorded in 13 PRA-affected cases revealed non-recordable extinguished (flatline) ERG responses. A reduction mainly of a- and b-wave amplitudes in the ERG indicated a generalized photoreceptor disease.
dog
Electroretinography
Funduscopy
Progressive retinal atrophy
2017
06
01
119
123
https://ijvr.shirazu.ac.ir/article_4096_867c7031859b1c4cfbc144adc52b332a.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
p-cresol and oleic acid as reliable biomarkers of estrus: evidence from synchronized Murrah buffaloes
S.
Muniasamy
R.
Muthu Selvam
S.
Rajanarayanan
V.
Ramesh Saravanakumar
G.
Archunan
Successful reproductive management in buffaloes depends on effective estrus detection. Urinary pheromones identified from natural estrous cycle have been reported to decipher estrus phase. However, its presence has not been analyzed in the urine after synchronization. Thus, our present investigation was to investigate the influence of synchronized estrus urine in bulls and to examine the presence of estrus-specific compounds ascertained in natural estrus in synchronized buffaloes. Mid-stream urine was collected from six synchronized buffaloes during various phases of estrous cycle and volatiles were examined using GC-MS. Sexual provocation in bulls was established by displaying persistent flehmen and frequent mounting towards estrus urine from synchronized animals. Totally forty-two volatile compounds were identified from three phases of estrous cycle, more specifically 4-methyl phenol (p-cresol) and 9-octadecenoic acid (oleic acid) in estrus urine of synchronized animal as similar to natural estrus. Hence, these chemical cues in buffalo urine might be employed as potential marker candidates for the development of an estrus detection aid.
CIDR
Flehmen
Mating
4-methyl phenol
9-octadecenoic acid
2017
06
01
124
127
https://ijvr.shirazu.ac.ir/article_4097_a0658615423f4a8093382e98852aed25.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
Co-relation of estrous cycle phases with uterine bacterial and fungal flora in non-pregnant female laboratory rabbits
A.
Mogheiseh
A.
Derakhshandeh
E.
Batebi
N.
Golestani
A.
Moshiri
This study was designed to investigate the relationship between the estrous cycle phases with uterine bacterial and fungal flora in non-pregnant female rabbits. Thirty laboratory mature multiparous rabbits were used for this purpose. Samples from uterine lavage for culture of bacteria and fungi were collected at different stages of estrous cycle (based on vaginal cytology), and histopathological observations were evaluated based on the scoring system used for defining the infection of the uterus. Various types of bacteria and fungi were isolated from rabbits at all stages of estrous cycle. The widest variety of bacteria and fungi was isolated at Di-estrous stage and the lowest variety was detected at estrous stage. Klebsiella oxytoca as well as yeast have been isolated at all stages of estrous cycle. This study showed that infection with K. oxytoca and yeast had no relationship with different stages of estrous cycle but other bacteria and fungus were associated with one or more stages of the estrous cycle in rabbits.
Bacterial flora
Estrous cycle
Female rabbit
Fungi
Uterus flushing
2017
06
01
128
133
https://ijvr.shirazu.ac.ir/article_4098_bfd9733aaafbc2b055f6fdfa2ece31b8.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
LAMP assay for rapid diagnosis of cow DNA in goat milk and meat samples
R.
Deb
G. S.
Sengar
U.
Singh
S.
Kumar
T. V.
Raja
R.
Alex
R. R.
Alyethodi
B.
Prakash
Animal species detection is one of the crucial steps for consumer’s food analysis. In the present study we developed an in-house built loop-mediated isothermal amplification (LAMP) assay for rapid detection of adulterated cow DNA in goat milk/meat samples. The cow milk/tissue DNA in goat milk/meat samples were identified in the developed LAMP assay by either naked eye visualizing with SYBR Green I dyes or by detecting the typical ladder pattern on gel electrophoresis. This test can detect up to minimum 5% level of cow components admixed in goat milk/meat samples and can be completed within 1 h 40 min starting from DNA extraction from milk/meat samples and can be performed in a water bath. Developed LAMP methodology is simple; rapid and sensitive techniques that can detect adulterant like cow components in goat milk/meat are more accurate than other existing DNA based technologies.
Cow
Goat
LAMP assay
Meat
Milk
2017
06
01
134
137
https://ijvr.shirazu.ac.ir/article_4099_33749f0271c58f2cf4d9b5c9da45608d.pdf
Iranian Journal of Veterinary Research
IJVR
1728-1997
1728-1997
2017
18
2
Use of locking plate in combination with dynamic compression plate for repair of tibial fracture in a young horse
R. A.
Ahmad
H. P.
Aithal
D. N.
Madhu
-
Amarpal
P.
Kinjavdekar
A. M.
Pawde
Grade 1 open spiral fracture of left tibia in a 1.5 year-old horse was treated using a combination of 4.5 mm locking compression plate (LCP) and a dynamic compression plate applied in a neutralization manner. The open wound was managed postoperatively by regular dressing and lavage. Radiograph at 24 days post-treatment revealed callus formation and at two months complete bridging callus was observed. At the end of six months complete healing of the fracture with functional recovery of the limb was observed.
Fracture
horse
Locking plate
Tibia
2017
06
01
138
141
https://ijvr.shirazu.ac.ir/article_4100_1334741ee65fe9ac938338d0fadaf109.pdf