Evaluation of some haematological variables of Acipenser persicus and Acipenser stellatus at different water temperaures

Some haematological variables including Red Blood Cells (RBC), White Blood Cells (WBC) differential counts, Haemoglobin (Hb), Haematorite (HCT), Mean Corpuscular Volume (MCV), Mean Corpuscular Haemoglobin (MCH) and Mean Corpuscular Haemoglobin Concentration (MCHC) were measured in 90 stellate sturgeon juveniles Acipenser stellatus (1-2 years old) and 90 Persian sturgeons Acipenser persicus (1-2 years old) at different water temperature 10-15C, 16-20?C and 21-25C. Also these parameters were evaluated in 84 adult including A. persicus (54 samples) and A. stellatus (30 samples) collected from Caspian Sea during spring and autumn 1997. The results have showed that WBC differential counts, Hb, HCT, MCV and MCH were identical for both species at the mentioned water temperatures. However, the values for RBC of A. persicus were generally less than those of A. stellatus. These haematological factors relatively increased with the water temperature increasing. Although RBC and WBC values of A. persicus were less than those of A. stellatus. The rates for HCT, MCV and MCH were higher in A. persicus

Теоретичні основи безпосереднього народовладдя

Розглядаються такі форми безпосереднього народовладдя, як мітинги, збори, демонстрації. Подано пропозиції щодо удосконалення чинного законодавства, яке регулює проведення зборів, мітингів, демонстрацій в Україні.Рассматриваются такие формы непосредственного народовластия, как митинги, собрания, демонстрации. Поданы предложения по совершенствованию действующего законодательства, регулирующего проведение собраний, митингов, демонстраций в Украине.Such forms of democracy as mass meeting, collections, demonstrations are examined in this article. Insufficiency of set problem was emphasized. Suggestions are given concerning current legislation improvement related to collections, mass meeting, demonstrations realization in Ukraine

First isolation and identification of Vibrio vulnificus (biotype 2) from cultured beluga, huso huso in Iran

By decreasing sturgeon stocks in the Caspian Sea, rearing different sturgeon species especially Huso huso was increased in Iran. Under stress conditions the sturgeon can easily be infected by several opportunistic pathogens. In June 2011, mortality happened in 25 - 28°C water temperature, in one of the most important cultured sturgeon farms in Mazandaran province, north of Iran. The mortality rate was 15%. The first clinical signs in moribund fish were lethargy and anorexia. A total of 20 moribund fish was transferred to a central laboratory for more bacteriological examination. Clinical signs including several deep ulcers on body surface, around the head, under operculum, ulcers at the base of the pectoral fins, hemorrhage around the anus, operculum, and pale gills were observed in moribund fish. The main internal signs were hepatomegaly and splenomegaly, liquid accumulation in the intestine and diffuse visceral hemorrhage. The results of morphology and microscopic characterizations and also biochemical tests indicated that Vibrio vulnificus (biotype 2) was the etiological agent of mortality in infected fish. This study was the first report of V. vulnificus in cultured H. huso in Iran

Floristic characteristics of the Hyrcanian submountain forests (case study: Ata-Kuh forest)

Ata-Kuh forest, a preserved area within Hyrcanian relict forests, with an area of 700 ha is located in north of Iran. Based on floristic studies from 2011 through 2012, 194 vascular plant species were identified belonging to 143 genera and 66 families. Among our samples, 24 taxa were endemic to Hyrcanian area. The largest families in the area were Rosaceae (10.3 %), Poaceae (9.7 %), Asteraceae (6.7 %), Fabaceae (5.6 %) and Lamiaceae (5.1 %). The genera represented by the greatest number of species were Rubus (8 species), Carex (7 species), Viola and Euphorbia (each with four species). Classification based on life form indicated that geophytes comprise the largest proportion of the plants in the studied area. From the chorological point of view, the largest proportion of the flora belonged to the Euro-Siberian elements (60 taxa, 31.1%). In this study, a comparison was performed between our results and other studies on the northern Iranian forests with respect to life forms and phytochoria. Psilotum nodum is reported here again from a new locality in North Iran, indicating the old Tertiary history of this forest

Survey on achieving recombinant DNA vaccine (live delivery) against streptococcosis for Rainbow trout (Oncorhynchus mykiss) immunization

The main purpose of this study was survey on achieving recombinant DNA vaccine (live delivery) against streptococcusis for Rainbow trout (Onchorhynchus mykiss) Immunization. Initially, a total of 515 samples were collected from the head kidney of diseased fish (weigh 50_ 200g) in 72 farms of 8 provinces. Approximately, 40% (206 samples) of specimens were infected to Streptococcus species. Then were isolated 172 DNA samples and consequently, five pathogenic species have been identified, including S. iniae, S. faecium, S. agalactiae, S. dysgalatiae, and S. uberis. The enzyme phosphoglucomutase (PGM) has recently been discovered to play an important role in polysaccharide capsule production and virulence in S. iniae. Therefore, was initially isolated S. iniae and cloning phosphoglucomutase gene. Then, the PGM gene was amplified successfully and cloned in pTZ57R cloning vector. The recombinant plasmid was sub cloned into pETD uet-l expression vector by restriction enzymes and confirmed by PCR. Meanwhile, for amplifying simA and cpsD genes were used universal primers pNZ8148 and special for simA and cpsD genes.The recombinant bacteria Lactococcus lactis (NZ9000) was used for transformation the plasmid into Lactococcus lactis. Vaccination was performed by oral, bath and injection (peritoneal) methods. The efficiency of g2 was better than g1in these three methods and all of groups. The determination of IgM level, or detection of anti S. iniae antibody was carried out by using ELISA. The results revealed that there was a significant (p<0.05) difference between the level of IgM in all three methods and experiment groups compare to control group. The results of challenge of vaccinated fish with S. iniae showed that fish RPS in all of groups except group 3 (42.63 percent) were more than 50 percent while, in control group was 21.43 percent. The highest fish RPS was belong to group 11(61.25 percent) and statistical analyses revealed that significant (p<0.05) difference between fish vaccinated RPS, compare to control group

Study of genotype, subtype and mutation in the S gene in hepatitis B patients co-infected with HIV in Iran

Background: Co-infection with human immunodeficiency virus (HIV) and hepatitis B virus (HBV) is common due to shared routes of transmission, as reported approximately 10% of 33 million HIV-infected patients worldwide are chronically infected with HBV. Mutations of HBsAg especially within the “a” determinant could alter the antigenicity of the protein, causing failure of HBsAg neutralization and escaping from the host’s immune system. This results in active viral replication and liver disease. Objectives: The aim of the survey was to identify HBV genotype and subtype, and different mutations in HBV S gene in hepatitis B patients co-infected with HIV in Iran. Methods: PCR performance and HBV-DNA extraction from plasma of 124 samples obtained from treatment naive HIV/HBV coinfected participants were according to the protocol. Direct sequencing and alignment of surface gene were carried out using reference sequences from the Gene Bank database. Results: From 124 HIV/HBV ELISA positive samples, 40 were HBV DNA-positive. Themean age of patients was 33.88 years. 20% of them were female and 80% were male. All isolates belonged to the sub genotype D1/ayw2 and genotype D. There were 50 point mutations including 23 (46%) missense and 27 (54%) silent mutations in amino acid level. Twenty three amino acid mutations occurred in different immune epitopes such as 11 (47.82%) in B cell, 6 (26.08%) in T helper and 2 (%8.6) in CTL. The prevalence of mutations in both “a” determinant region and Major Hydrophilic Region (MHR) was 5 (21.73%). Conclusions: Our findings showed that P127T and A70P (Outside of MHR) were the most frequently occurring substitution mutations. P127T, P132T, G130R, and S136Y substitutions placed in the first loop of the “a” determinant and the other substitutions of P142T and D144N occurred in the second loop of “a” determinant. The results of our study showed that most of the mutations occurred in B cell epitopes. The mutation in a surface gene of HBV may be selected by immune pressure or anti-retroviral therapy

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome).

BACKGROUND: Putative nucleotidyltransferase MAB21L1 is a member of an evolutionarily well-conserved family of the male abnormal 21 (MAB21)-like proteins. Little is known about the biochemical function of the protein; however, prior studies have shown essential roles for several aspects of embryonic development including the eye, midbrain, neural tube and reproductive organs. OBJECTIVE: A homozygous truncating variant in MAB21L1 has recently been described in a male affected by intellectual disability, scrotal agenesis, ophthalmological anomalies, cerebellar hypoplasia and facial dysmorphism. We employed a combination of exome sequencing and homozygosity mapping to identify the underlying genetic cause in subjects with similar phenotypic features descending from five unrelated consanguineous families. RESULTS: We identified four homozygous MAB21L1 loss of function variants (p.Glu281fs*20, p.Arg287Glufs*14 p.Tyr280* and p.Ser93Serfs*48) and one missense variant (p.Gln233Pro) in 10 affected individuals from 5 consanguineous families with a distinctive autosomal recessive neurodevelopmental syndrome. Cardinal features of this syndrome include a characteristic facial gestalt, corneal dystrophy, hairy nipples, underdeveloped labioscrotal folds and scrotum/scrotal agenesis as well as cerebellar hypoplasia with ataxia and variable microcephaly. CONCLUSION: This report defines an ultrarare but clinically recognisable Cerebello-Oculo-Facio-Genital syndrome associated with recessive MAB21L1 variants. Additionally, our findings further support the critical role of MAB21L1 in cerebellum, lens, genitalia and as craniofacial morphogenesis