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2.
Microb Pathog ; 123: 377-384, 2018 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-30053605

RESUMEN

Camel Anaplasmosis is caused by members of family Anaplasmatacae, a tick transmitted, obligate intracellular bacteria. The etiological bacteria are transmitted by ixodid tick species. The species have multi host range distribution that is why it is crucial to diagnose it timely. The aim of present study was to investigate the molecular epidemiology i.e. prevalence and risk factors analysis of camel anaplasmosis. Furthermore, variations in hematological standards were also evaluated. The study found an overall 13.33% prevalence in camels. The confirmation of PCR positive samples for Anaplasma spp. was made through sequencing, the study isolatesshowed high homology with Iranian, Chinese, Philippines and South African isolates of Anaplasmatacae (Accession numbers'; KX765882, KP062964, KY242456, LC007100 and U54806) on BLAST queries. The phylogenetic analysis revealedthree study isolates of present study clustered with each other and the cluster was found closer to Chinese isolate of A. phagocytophilum (KY242456), A. marginale (KU586048), and Mongolian isolates of A. ovis (LC194134). Two of the isolates resembled Iranian isolate of Candidatus Anaplasmacamelii (KX765882), while one isolate resembled with Chinese isolates of A. Platys (KX987336) and Croatian isolates of A. Platys (KY114935). The key risk factors odds ratio (OR>1) identified for occurrence of camel anaplasmosis using regression model found sex and age of animal, previous tick history, tick infestation and tick control status, housing type, cracks in walls, rearing system and other species in surrounding as the key risk factors. The hematological parameters like lymphocytes, monocytes, granulocytes and platelets count were significantly decreased (p < 0.05) in diseased camels than healthy. This is the first ever molecular data on camel anaplasmosis in Pakistan. The disease should be monitored unceasingly as the etiologies have multi host distribution. Prompt attention should be offered to animals because neutropenia, lymphopenia and thrombocytopenia can exacerbate the disease by making the animal predisposed to otherdiseases.


Asunto(s)
Anaplasma/clasificación , Anaplasma/genética , Anaplasma/patogenicidad , Anaplasmosis/epidemiología , Anaplasmosis/microbiología , Camelus/microbiología , Epidemiología Molecular , Filogenia , Factores de Edad , Anaplasma/aislamiento & purificación , Anaplasmosis/sangre , Anaplasmosis/genética , Enfermedades de los Animales/epidemiología , Animales , ADN Bacteriano/sangre , Pruebas Hematológicas , Linfopenia , Neutropenia , Pakistán/epidemiología , Prevalencia , ARN Ribosómico 16S/genética , Análisis de Regresión , Factores de Riesgo , Homología de Secuencia de Ácido Nucleico , Factores Sexuales , Trombocitopenia , Garrapatas/microbiología
3.
Microb Pathog ; 120: 176-180, 2018 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-29733903

RESUMEN

Blackleg is an endogenous acute infection that principally affects cattle. The disease is caused by Clostridium chauvoei (C. chauvoei), an anaerobic spore forming bacterium. Control of this disease is based on stringent husbandry measures and scheduled vaccination plan. In recent years, the major virulence factors of C. chauvoei have been discovered and described. However, the pathogenesis of blackleg in cattle and in particular, circulation of the pathogen from point of entry to target tissues is yet not fully elucidated. This review summarizes the latest review of literature that significantly contributed for understanding the disease in cattle, and provides a foundation to preventive strategies.

4.
Trop Biomed ; 35(2): 434-441, 2018 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-33601817

RESUMEN

Clostridium perfringens (C. perfringens) is a normal inhabitant in the gut of animals. It may proliferate rapidly in favorable conditions and produces lethal toxins. These toxins may cause lethal effects in the intestines and systemically it may cause enterotoxaemia. In disease conditions, the presence of C. perfringens CFU/g in fecal sample can be of diagnostic value. This study aims to determine the bacterial counts and predisposing factors of C. perfringens (targeting CPA gene) infection in addition to an in-vitro antimicrobial trial in entero-toxemic sheep in Pakistan. A total of 192 diarrheic sheep irrespective of age, gender and breed were selected and the CFU/g was determined from the fecal samples. The study showed that 34.9% of the samples had elevated level of bacterial count compared to the normal (104-107 CFU/g). Out of the total, 7.8% of the samples had subnormal bacterial count (CFU/g), while, 57.3% of the samples showed bacterial counts in the normal ranges. The confirmation of selectively isolated C. perfringens was done by amplification of 324bp CPA gene fragment using polymerase chain reaction (PCR). The in-vitro antimicrobial sensitivity trials showed that penicillin, ciprofloxacin and ceftriaxone are 100% efficacious against C. perfringens, while, bacitracin, ampicillin and amoxicillin were found to be least effective. The key determinants in this study which support the in-vivo growths of C. perfringens were; carbohydrate rich diet and overcrowding with the odds ratios (OR) of 5.44 and 2.26, respectively. This study concludes that C. perfringens is highly prevalent in sheep population of Pakistan. The incidence of enterotoxaemia can be minimized by controlling the factors which enhance its in-vivo growth. The diseased animal associated with elevated C. perfringens levels can be effectively cured using any one of the penicillin, ciprofloxacin and ceftriaxone.

5.
Horm Res Paediatr ; 79(5): 310-7, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23651953

RESUMEN

BACKGROUND: Leptin deficiency is associated with severe obesity and metabolic disturbances. Increased liver fat content has been reported in only one case beforehand, even though hepatic steatosis is a typical comorbidity of common obesity. It is also frequent in patients with lipodystrophy where it resolves under leptin therapy. SUBJECT AND METHODS: In 2010, we reported a leptin-deficient patient with a novel homozygous mutation in the leptin gene and severe hepatic steatosis. We have now studied serum changes and changes in liver fat content during the substitution with recombinant methionyl human leptin. RESULTS: After 23 weeks of leptin substitution, elevated transaminases, total cholesterol and low-density lipoprotein levels normalized. After 62 weeks, homeostasis model assessment of insulin resistance improved from 10.7 to 6.0 and body fat mass dropped from 50.2 to 37.8%. Liver fat content was drastically reduced from 49.7 to 9.4%. The first changes in liver fat content were detectable after 3 days of therapy. CONCLUSION: Our patient showed a remarkable reduction of liver fat content during the treatment with recombinant methionyl human leptin. These changes occurred rapidly after initiation of the substitution, which implies that leptin has a direct effect on hepatic lipid metabolism in humans as it is seen in rodents.


Asunto(s)
Hígado Graso/sangre , Hígado Graso/tratamiento farmacológico , Terapia de Reemplazo de Hormonas , Leptina/deficiencia , Leptina/uso terapéutico , Adolescente , Colesterol/sangre , Hígado Graso/patología , Hígado Graso/fisiopatología , Femenino , Homocigoto , Humanos , Leptina/genética , Lipoproteínas LDL/sangre , Hígado/metabolismo , Hígado/patología , Hígado/fisiopatología , Mutación , Factores de Tiempo
6.
Int J Obes (Lond) ; 31(9): 1437-41, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17356525

RESUMEN

BACKGROUND: Previous studies have suggested that a variant in the melanocortin-4 receptor (MC4R) gene is important in protecting against common obesity. Larger studies are needed, however, to confirm this relation. METHODS: We assessed the association between the V103I polymorphism in the MC4R gene and obesity in three UK population based cohort studies, totalling 8304 individuals. We also did a meta-analysis of relevant studies, involving 10 975 cases and 18 588 controls, to place our findings in context. FINDING: In an analysis of all studies, individuals carrying the isoleucine allele had an 18% (95% confidence interval 4-30%, P=0.015) lower risk of obesity compared with non-carriers. There was no heterogeneity among studies and no apparent publication bias. INTERPRETATION: This study confirms that the V103I polymorphism protects against human obesity at a population level. As such it provides proof of principle that specific gene variants may, at least in part, explain susceptibility and resistance to common forms of human obesity. A better understanding of the mechanisms underlying this association will help determine whether changes in MC4R activity have therapeutic potential.


Asunto(s)
Predisposición Genética a la Enfermedad , Obesidad/genética , Polimorfismo Genético , Receptor de Melanocortina Tipo 4/genética , Alelos , Índice de Masa Corporal , Estudios de Cohortes , Genética de Población , Heterocigoto , Humanos , Masculino , Persona de Mediana Edad , Fenotipo
7.
Phys Rev Lett ; 93(6): 063001, 2004 Aug 06.
Artículo en Inglés | MEDLINE | ID: mdl-15323624

RESUMEN

In the laser excitation of ultracold atoms to Rydberg states, we observe a dramatic suppression caused by van der Waals interactions. This behavior is interpreted as a local excitation blockade: Rydberg atoms strongly inhibit excitation of their neighbors. We measure suppression, relative to isolated atom excitation, by up to a factor of 6.4. The dependences of this suppression on both laser irradiance and atomic density are in good agreement with a mean-field model. These results are an important step towards using ultracold Rydberg atoms in quantum information processing.

8.
Phys Rev Lett ; 91(18): 183002, 2003 Oct 31.
Artículo en Inglés | MEDLINE | ID: mdl-14611280

RESUMEN

We present evidence for molecular resonances in a cold dense gas of rubidium Rydberg atoms. Single UV photon excitation from the 5s ground state to np Rydberg states (n=50-90) reveals resonances at energies corresponding to excited atom pairs (n-1)d+ns. We attribute these normally forbidden transitions to avoided crossings between the long-range molecular potentials of two Rydberg atoms. These strong van der Waals interactions result in avoided crossings at extremely long range, e.g., approximately 58 000 times the Bohr radius (a(0)) for n=70.

9.
Pituitary ; 2(1): 79-88, 1999 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-11081176

RESUMEN

In this review we discuss the physiological effects of somatostatin, which are mediated by specific receptor subtypes on different tissues. These observations have suggested new therapeutic possibilities for the use of the synthetic somatostatin analogues in the treatment of acromegaly as well as a number of other endocrine and non-endocrine disorders.


Asunto(s)
Acromegalia/tratamiento farmacológico , Antagonistas de Hormonas/uso terapéutico , Somatostatina/análogos & derivados , Somatostatina/uso terapéutico , Antagonistas de Hormonas/efectos adversos , Humanos , Neoplasias Hipofisarias/tratamiento farmacológico , Somatostatina/efectos adversos
11.
Int J Cardiol ; 47(1): 45-9, 1994 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-7868284

RESUMEN

A high cardiovascular mortality rate exists amongst people of Indo-origin in Trinidad (third generation migrants) and the United Kingdom (first generation migrants). To investigate the differences in cardiovascular risk factors in these two populations, we surveyed all male patients of Indo-origin with acute myocardial infarction, admitted over a similar 8-week period to the Coronary Care Units of a district general hospital in Birmingham, United Kingdom and a similar hospital in San Fernando, Trinidad. Nineteen patients (mean age 62.2 years +/- S.D. 2.58) were admitted to the Birmingham hospital (UK Group) and fifty-five (mean age 58.1 years +/- S.D. 1.44) to the San Fernando hospital (Trinidad Group). There was no age difference between the groups (P = 0.18). There was a significantly greater proportion of smokers in the Trinidad group (70.9% vs. 63.2%, chi 2 = 4.56, P = 0.03), which also had a higher proportion of diabetics (36.4% vs. 31.6%) and hypertensives (34.5% vs. 31.6%). Mean systolic and diastolic blood pressures were higher in hypertensives from the Trinidad group (Trinidad group 146.6 mmHg +/- 16.9/93.4 mmHg +/- 11.4 vs. UK group 120.8 mmHg +/- 25.4/75.0 mmHg +/- 13.4; P < 0.05). The mean waist to hip ratio was greater in the Trinidad group (1.01 +/- S.D. 0.06) when compared to the UK group (0.95 +/- S.D. 0.05) (paired t-test, P < 0.01). Only six Trinidadian males performed regular exercise and only four of the UK group did so.(ABSTRACT TRUNCATED AT 250 WORDS)


Asunto(s)
Infarto del Miocardio/etnología , Asia/etnología , Distribución de Chi-Cuadrado , Diabetes Mellitus , Humanos , Hipertensión , Masculino , Persona de Mediana Edad , Infarto del Miocardio/epidemiología , Obesidad , Factores de Riesgo , Fumar , Factores Socioeconómicos , Trinidad y Tobago/epidemiología , Reino Unido/epidemiología
12.
Early Hum Dev ; 38(3): 209-13, 1994 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-7821265

RESUMEN

Certain infant care practices have consistently been shown to play an important role in the aetiology of the sudden infant death syndrome (SIDS). In the UK, the incidence of SIDS amongst Asians is less than half that of whites. We conducted a questionnaire-based survey of 374 multiparous mothers from a multiracial community in Birmingham. We found that the majority of Asian infants slept in the parental bedroom at night, 94% compared to 61% of whites, whilst 33% of white infants slept alone compared to 4% of Asians. Three times as many white mothers as Asians placed infants prone (31% vs. 11%). We, therefore, observed marked differences in the infant care practices of Asians compared to whites in the UK, which may partly account for the low incidence of SIDS amongst infants of Asian origin.


Asunto(s)
Cuidado del Lactante/métodos , Muerte Súbita del Lactante/etnología , Adulto , Asia/etnología , Lechos , Recolección de Datos , Inglaterra/epidemiología , Familia , Humanos , Incidencia , Lactante , Posición Prona , Sueño , Población Blanca
13.
Paediatr Perinat Epidemiol ; 7(3): 245-52, 1993 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-8378167

RESUMEN

The aetiology of sudden infant death syndrome (SIDS) is still uncertain, although associations with overheating and the prone sleeping position have been reported. In the UK, the incidence of SIDS is considerably lower in infants of Asian origin, but as yet no explanation for this has been suggested. We have studied a group of 202 white and 172 Asian multiparous mothers attending an antenatal clinic to compare the sleeping position and home environment of infants in each ethnic group. We found that significantly more white infants (31%) than Asians (11%) were placed in the prone position at night and that 94% of Asian infants slept in their parents' bedroom, compared with 61% of whites. These observations demonstrate marked differences in the infant rearing practices favoured by Asians and whites and lend support to the concept that the prone position and separate bedrooms may be contributors to the development of sudden infant death.


Asunto(s)
Etnicidad , Muerte Súbita del Lactante/etnología , Crianza del Niño , Preescolar , Inglaterra/epidemiología , Femenino , Vivienda , Humanos , India/etnología , Recién Nacido , Madres , Pakistán/etnología , Posición Prona , Sueño , Muerte Súbita del Lactante/etiología
14.
BMJ ; 305(6849): 369, 1992 Aug 08.
Artículo en Inglés | MEDLINE | ID: mdl-1392908
16.
Cathet Cardiovasc Diagn ; 11(6): 597-601, 1985.
Artículo en Inglés | MEDLINE | ID: mdl-2868797

RESUMEN

The first reported case of a patient with left internal mammary artery bypass graft dissection secondary to selective coronary and graft arteriography is presented. The intimal tear and false lumen could not be seen with flouroscopy during catheterization. This later led to antero-septal myocardial infarction.


Asunto(s)
Cateterismo Cardíaco/efectos adversos , Revascularización Miocárdica , Enfermedad Coronaria/etiología , Femenino , Humanos , Arterias Mamarias/diagnóstico por imagen , Persona de Mediana Edad , Revascularización Miocárdica/efectos adversos , Radiografía
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