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Vaginal infection It is one of the most common illnesses in the world. affecting women's health, with more than half of all women experiencing at least one episode in their lifetime. Vaginal disease can be both infectious and chronic. Bacterial vaginosis (BV), vaginal candidiasis, and vaginal trichomonas are the three most common types of infectious vaginitis based on microbial etiology (Abdul-Aziz et al., 2019). Antimicrobial-resistant (AMR) infections are caused by microbes that are resistant to antimicrobial agents. As bacteria develop resistance, many previously effective drugs no longer work (Ali, 2018). Each year, AMR infections kill 700,000 people around the world. By 2050, antimicrobial resistance may be responsible for the deaths of up to 10 million people annually. De Kramer and colleagues (2016): According to a recent research study (Amirkamali et al., 2017), antibiotic resistance genes blab-TEM may be able to predict the presence of antibiotic resistance in bacteria.

Bacillus cereus is a Gram positive rod-shape bacterium, that causes severe food poisoning. Bacillus form spores that enable it to resist the environmental stresses, such as drought, heat, pH changes. Spores can remain dormant for many years, and back to the vegetative cells when suitable conditions available for bacterial growth. Several food poisoning outbreaks in cereal products showed that B. cereus was the main causative agent. Recently, the multiplex polymerase chain reaction (m-PCR) has provide a rapid and highly sensitive method for the detection of specific pathogenic microorganisms in the aquatic environment. To date, most m-PCR assays for pathogen detection have focused on only one, two or three different types of organisms. The lack of knowledge in the development of a multiplex PCR assay for the specific detection of Bacillus cereus inspire us to spot the light on the development of the method for Bacillus cereus detection in one rapid multiplex PCR assay and the potential application of Response Surface Methodology (RSM) for the simultaneous detection of other multi-pathogen systems.

Sudden death is usually the main finding in field animals during haemorrhagic septicaemia outbreaks caused by Pasteurella multocida type B:2 that causes acute, fatal and septicaemic disease in cattle and buffaloes. This situation may be due to failure in early detection of the disease where early treatment of antibiotics may improve the prognosis of the animal and other surviving animals. Thus, there is a grey area on the knowledge on the potential usage of pro-inflammatory cytokines and acute phase proteins as early biomarkers in the diagnosis of haemorrhagic septicaemia. In addition, exploration of the cerebrospinal fluid during infection has never been studied before. Therefore, this study was designed to fill up the grey areas in haemorrhagic septicaemia research. Twenty-one buffalo calves were divided into seven treatment groups where group 1 was inoculated orally with 10 mL of sterile phosphate-buffered saline pH 7 which act as a negative control group. Groups 2 and 3 were inoculated orally and subcutaneously with 10 mL of 1012 colony-forming unit of P. multocida type B:2. Group 4 and 5 buffaloes were inoculated orally and intravenously with 10 mL of lipopolysaccharide broth. Groups 6 and 7 were administered orally and subcutaneously with 10 mL of outer membrane protein broth. During the post-infection period of 21 days, blood and cerebrospinal fluid were sampled for the analyses of pro-inflammatory cytokines, acute phase proteins and cytological examination. Buffalo calves infected with P. multocida and its immunogens via different routes of inoculation showed significant changes (p

The purpose of the present study is to evaluate the effect sub minimum inhibitory concentration (MIC) of imipenem, amikacin and cefixime on growth and swarming of Proteus mirabilis. 10 clinical isolates of Proteus mirabilis were isolated from patients suffering from urinary tract infection. 3 types of antibiotics include imipenum, amikacin and cefixime were used in present study to detect their ability to inhibition the swarming of P. mirabilis. Each isolate were inoculated on a series of nutrient agar containing different concentrations (60, 30, 15, 7.5, 3.75, 1.8 and 0.9 µg/ml) of imipenem, cefixime and amikacin. All these were incubated over night at 37°C, after that the cultivated bacterial growth examined to determine the effect of each antibiotic on growth and swarming of P. mirabilis. The results showed that the 0.93 µg/ml of imipenem have ability to inhibit the swarming of all isolates (100%) and it have not any effect on growth (bacterial growth 100%) whereas the same concentration of cefixime inhibit 90% of isolate and also have not any effect on growth (bacterial growth 100%). The results of amikacin showed that the 0.93 µg/ml of antibiotic inhibit the swarming 50% of isolate and the bacterial growth was 100%. Imipenem have good inhibiter effect on Proteus mirabilis swarming at concentration of 0.93 µg/ml and we suggest that we can use this antibiotic to prepare cultural media to separate mixed culture contain P. mirabilis.

Hemorrhagic septicemia (HS) is a globally renowned disease that affects cattle and buffaloes. Its effects on the reproductive system have not been previously studied. Thus, the present study aims to evaluate the pathological responses in pre-pubertal female buffalo infected with immunogens; lipopolysaccharide (LPS) and outer membrane protein (OMP) derived from P. multocida type B: 2. Fifteen healthy pre-pubertal female buffaloes of approximately 8 months old were selected and divided into five equal groups of 3 buffaloes each. Buffaloes in groups 1 and 2 were intravenously and orally inoculated with 10 mL of P. multocida LPS at 1× 1012 colony forming unit (cfu) ,while those in group 3 and group 4 were subcutaneously and orally inoculated with10 mL of P. multocida OMP at 1× 1012 colony forming unit (cfu). Buffaloes in group 5 were inoculated with 10mL of sterile phosphate buffered saline (PBS) PH7 and served as the negative control. During the post infection period, all buffaloes were examined for clinical signs throughout 21 days and surviving buffaloes were euthanized for postmortem evaluation. Histopathological evaluation of buffaloes inoculated with LPS showed a significantly higher occurrence (p

Lipopolysaccharide (LPS) of P. multocida B:2, a causative agent of haemorrhagic septicaemia (HS) in cattle and buffaloes, is considered as the main virulence factor and contribute in the pathogenesis of the disease. Recent studies provided evidences about the involvement of the nervous system in pathogenesis of HS. However, the role of P. multocida B:2 immunogens, especially the LPS is still uncovered. Therefore, this study was designed to investigate the role of P. multocida B:2 LPS to induce pathological changes in the nervous system. Nine eight-month-old, clinically healthy buffalo calves were used and distributed into three groups. Calves of Group 1 and 2 were inoculated orally and intravenously with 10 ml of LPS broth extract represent 1 × 1012 cfu/ml of P. multocida B:2, respectively, while calves of Group 3 were inoculated orally with 10 ml of phosphate buffer saline as a control. Significant differences were found in the mean scores for clinical signs, post mortem and histopathological changes especially in Group 2, which mainly affect different anatomic regions of the nervous system, mainly the brain. On the other hand, lower scores have been recorded for clinical signs, gross and histopathological changes in Group 1. These results provide for the first time strong evidence about the ability of P. multocida B:2 LPS to cross the blood brain barrier and induce pathological changes in the nervous system of the affected buffalo calves.

Haemorrhagic septicaemia (HS) is an acute, fatal, septicaemic disease of cattle and buffaloes caused by one of two specific serotypes of Pasteurella multocida B:2 and E:2 in Asian and African, respectively. It is well known that HS affect mainly the respiratory and digestive tracts. However, involvement of the nervous system in pathogenesis of HS has been reported in previous studies without details. In this study, nine buffalo calves of 8 months old were distributed into three groups. Animals of Group 1 and 2 were inoculated orally and subcutaneously with 10 ml of 1 × 10(12) cfu/ml of P. multocida B:2, respectively, while animals of Group 3 were inoculated orally with 10 ml of phosphate buffer saline as a control. All calves in Group 1 and Group 3 were euthanised after 504 h (21 day) post-infection, while calves in Group 2 had to euthanise after 12 h post-infection as they develop sever clinical signs of HS. Significant differences were found in Group 2 in the mean scores of clinical signs, gross and histopathological changes which mainly affect different anatomic regions of the nervous system. In addition, successful bacterial isolation of P. multocida B:2 were obtained from different sites of the nervous system. On the other hand, less sever, clinical, gross and histopathological changes were found in Group 1. These results provide for the first time strong evidence of involving of the nervous system in pathogenesis of HS, especially in the peracute stage of the disease.

Pasteurella multocida is responsible for one of the major animal diseases with economic importance in both developed and developing countries. P. multocida B:2 causes haemorrhagic septicemia (HS) in cattle and buffaloes, which result in heavy economic losses through direct effect, resulting in high mortality rates and indirect effects through impairment of the animal productivity. It is well known that HS affects mainly the respiratory and digestive tracts of host animals. However, involvement of the reproductive system in the pathogenesis of HS has not been reported previously. This study was designed to present detailed detection and histopathological changes of the reproductive system and mammary glands of buffaloes experimentally infected with P. multocida B:2. Briefly, nine healthy buffalo calves aged 8-month-old were divided into three groups of three calves each. Calves from groups 1 and 2 were inoculated subcutaneously and orally with 10 mL of 1 × 1012 cfu/mL of P. multocida B:2, respectively, while calves of group 3 were inoculated orally with 10 mL of phosphate buffer saline as a sham control. All the calves in group 1 had to be euthanized after 12 h post-infection, while calves in group 2 were euthanized after day 21 post-infection. Successful isolation and PCR confirmation of P. multocida B:2 was achieved from different parts of the reproductive system, including ovary, oviduct, uterine horn, uterine body and vagina as well as mammary glands and supramammary lymph nodes of the buffaloes in group 1 after 12 h post-infection. However, P. multocida B:2 was not detected in the reproductive organs of buffaloes in group 2 and group 3 after 21 days post-infection. Significant differences (P

Background: Pasteurella multocida a Gram-negative bacterium has been identified as the causative agent of many economically important diseases in a wide range of hosts. Hemorrhagic septicemia is a disease caused by P. multocida serotype B:2 and E:2. The organism causes acute, a highly fatal septicemic disease with high morbidity and mortality in cattle and more susceptible in buffaloes. Therefore, the aim of this study was to investigate the clinical signs, blood parameters, post mortem and histopathology changes caused by P. multocida Type B:2 infections initiated through the oral and subcutaneous routes. Methods: Nine buffalo heifers were divided equally into 3 treatment groups. Group 1 was inoculated orally with 10 ml of phosphate buffer saline; Groups 2 and 3 were inoculated with 10 ml of 1012 colony forming unit of P. multocida Type B:2 subcutaneously and orally respectively. Results: There was a significant difference (p

Pasteurella multocida was first shown to be the causative agent of fowl cholera by Louis Pasteur in 1881. Since then, this Gramnegative bacterium has been identified as the causative agent of many other economically important diseases in a wide range of hosts. Haemorrhagic Septicaemia (HS) is a disease, caused by Pasteurella multocida serotypes B2 and E2 that causes acute, highly fatal septicaemia with high morbidity and mortality in cattle and more susceptible in buffaloes. In this review, we aim to determine the host cell and antibody response towards Pasteurella multicoda B2 infection causing Haemorrhagic septicaemia.

Background Hemorrhagic septicemia is a fatal disease of cattle and buffaloes caused by P. multocida. Although the pathogenesis of the bacteria has been well established in literature, there is a paucity of information on the possible role of the bacteria and its immunogens; lipopolysaccharide (LPS) and outer membrane proteins (OMPs) on the reproductive capacity of buffalo heifers. Methods In this study, twenty one healthy prepubertal female buffaloes aged 8 months were divided into seven groups of 3 buffaloes each (G1-G7). Group 1 (G1) served as the negative control group and were inoculated orally with 10 mL sterile Phosphate Buffer Saline (PBS), groups 2 (G2) and 3 (G3) were inoculated orally and subcutaneously with 10 mL of 1012 colony forming unit (cfu) of P.multocida type B: 2, while groups 4 (G4) and 5 (G5) received 10 mL of bacterial LPS orally and intravenously, respectively. Lastly, groups 6 (G6) and 7 (G7) were orally and subcutaneously inoculated with 10 mL of bacterial OMPs. Whole blood was collected in EDTA vials at stipulated time points (0, 2, 4, 6, 8, 10, 12, 24, 36, 48, 72, 120, 168, 216, 264, 312, 360, 408, 456 and 504 h), while tissue sections of the pituitary glands were collected and transported to the histopathology laboratory in 10% buffered formalin for processing and Hematoxylin and eosin staining. Plasma levels of luteinizing hormone (LH), follicle stimulating hormone (FSH), progesterone (PG), estradiol (EST) and gonadotrophin releasing hormone (GnRH) were determined. Results The histopathological lesions observed in the pituitary gland included hemorrhage, congestion, inflammatory cell infiltration, hydropic degeneration, necrosis and edema. These changes were higher (p

Haemorrhagic septicaemia is a disease caused by Pasteurella multocida serotype B: 2 and E: 2. The organism causes acute, highly fatal septicaemic disease with high morbidity and mortality in cattle and more susceptible in buffaloes. Lipopolysaccharide can be found on the outer cell wall of the organism. Lipopolysaccharide is released during multiplication which leads to inflammatory reaction. It represents the endotoxin of P. multocida type B: 2 and responsible for toxicity in haemorrhagic septicaemia which plays an important role in the pathogenesis of the disease. Therefore, the aim of this study was to investigate the clinical signs, blood parameters, gross post mortem lesions and histopathology changes caused by P. multocida type B:2 immunogen lipopolysaccharide infections initiated through intravenous and oral routes of infection. 9 buffalo heifers were divided equally into 3 treatment groups. Group 1 was inoculated orally with 10 ml of phosphate buffer saline (PBS); Group 2 and 3 were inoculated with 10 ml of lipopolysaccharide broth intravenously and orally respectively. For the clinical signs, there were significant differences (p0.05) in temperature between the control, intravenous and oral group. In hematology and biochemistry findings, there were significant differences (p0.05) in erythrocytes, haemoglobin, PCV, MCV, lymphocytes, monocytes, eosinophils, GGT and albumin between the control, intravenous and oral group. However, there were no significant differences (p0.05) in the MCHC, leukocytes, band neutrophils, basophils, thrombocytes, plasma protein, icterus index, total protein, globulin and A:G ratio between intravenous and oral group. For Group 2 buffaloes, there were gross lesions in the lung, trachea, heart, liver, spleen, and kidney. In contrast, lesions were only observed in the lung, trachea and liver of Group 3 buffaloes. There were significant differences (p0.05) in hemorrhage and congestion; necrosis and degeneration; and inflammatory cells infiltration between experimental groups and control group. However, there were no significant differences (p0.05) in edema lesion between groups. In conclusion, this study is a proof that oral route infection of P. multocida type B:2 immunogen lipopolysaccharide can be used to stimulate host cell responses where oral vaccine through feed could be developed in the near future.

Hemorrhagic septicemia (HS) is an acute septicemic disease principally affecting cattle and buffaloes caused by specific serotypes B:2 and E:2 of Pasteurella multocida in Asia and Africa, respectively. Despite continuing researches on pathogenesis of P. multocida for several decades, the mechanisms by which these bacteria develop the diseases are poorly understood. Although the involvement of the nervous system in the disease progress of HS is rare under natural conditions, few reports indicated the involvement of the nervous system in outbreaks of HS in cattle and buffaloes. Additionally, recent pathogenesis studies in both mouse and buffalo experimental models reported the involvement of nervous system due to P. multocida B:2, with bacteriological and histopathological evidences. In this review, we summarized and discussed the updates on the involvement of the nervous system in pathogenesis of HS focusing on clinical signs, pathological and pathophysiological changes. [J Adv Vet Anim Res 2015; 2(3.000): 252-262]

Objectives: Bovine anaplasmosis is an arthropod-borne hemolytic disease of cattle which is caused by a rickettsia; Anaplasma marginale . Anaplasmosis is also called "Yellow bag" or yellow fever, where the affected animals usually develop a jaundiced appearance. The objective of this study was to investigate the clinical findings, treatment and gross pathology of a severe anaplasmosis in a dairy cow. Materials and methods: In this report, a rare case of fatal anaplasmosis in a 4 year old Jersey-Friesian cow, weighing about 200 kg was reported. Diagnosis was done based on clinical symptoms, blood examination for the presence of A. marginale , and biochemical analyses of blood. Leishman staining was done to check the A. marginale at the margin of erythrocytes. Treatment was instituted with blood transfusion and Oxytetracyline dosed at 20 mg/kg body weight and iron supplement containing 20 mL Cobaphos (containing Phosphorus 125mg + Cyanocobalamine 0.05 mg) and 20 mL Fercobsang containing Iron (as ammonium citrate) 1.75 mg, Cyanocobalamine (Vitamin B12) 0.025 mg, Nicotinamide (vitamin PP) 20 mg, Cobalt (as digluconate) 0.0067 mg, Benzyl Alcohol (E1519) 20.8 mg) were given intramuscularly. Results: The cow did not survive the infection as it eventually died of the disease. Post mortem examination showed gross evidence of splenomegaly, hepatomegaly, distended bile duct and generalized jaundice. Conclusion: Based on the consequence of this case report, preventive vector control, prompt and appropriate treatment and improved management practices are recommended in order to prevent clinical anaplasmosis cases among cattle. http://doi.org/10.5455/javar.2016.c150