Detección e identificación de Salmonella spp. en huevos para consumo humano, provenientes de diferentes localidades de Bogotá, Colombia, 2015 / Salmonella spp. isolation and identification in eggs for human consumption from different urban areas in Bogotá, Colombia, 2015

Objetivo: Determinar la prevalencia de Salmonella spp. en muestras de huevos para consumo humano en localidades de Bogotá. Materiales y métodos: Se obtuvieron 96 muestras en tiendas y plazas de mercado de 4 localidades de la ciudad. Se procesó de forma separada la cáscara y el contenido interno mediante métodos microbiológicos y moleculares para aislamiento e identificación Salmonella spp. Resultados: Se determinó una prevalencia total de Salmonella spp. de 9,4% (n=9), de ésta el 55% (n = 5) provenían del contenido interno y 44% (n = 4) de cáscara, sin embargo no se logró tipificar el serovar de Salmonella enterica presente. Las localidades con mayor presencia del patógeno fueron Usaquén y Fontibón. Discusión: Estudios realizados en Colombia evidencian bajas prevalencias de Salmonella spp. (0 -1,74%) en muestras de huevos, sin embargo los hallazgos de este estudio evidencian una mayor recuperación, lo que podría asociarse con inadecuadas condiciones de manejo y/o almacenamiento del producto. Conclusión: Se estableció la presencia de Salmonella spp. en las muestras de huevo evaluadas, lo que implica un riesgo potencial para la salud pública, por lo que es necesario ampliar este tipo de estudios para conocer la situación real a nivel nacional frente a este patógeno.

Objective: To determine the prevalence of Salmonella spp presence in eggs for human consumption in urban areas in Bogota. Materials and methods: 96 samples were collected from convenience stores and markets in 4 urban areas in the city. The eggshells were separated from the egg's internal content and both were processed separately using microbiological and molecular techniques to isolate and identify Salmonella spp. strains. Results: A Salmonella spp. prevalence of 9.4% (n=9) was found. Salmonella spp was isolated from the egg's internal content in 55% (n=5) of samples and 44% (n=4) from the eggshells. The Salmonella enterica serovar could not be identified. The pathogen was more frequently isolate in samples from Usaquén and Fontibón urban areas. Discussion: Studies of Salmonella spp. prevalence in eggs done in Colombia have shown it to be low (0-1.74%); However, this study determined a higher prevalence. These results suggest that inadequate handling/storage conditions could have been associated with them. Conclusion: Salmonella spp. was isolated from the egg samples from 4 different urban areas in Bogotá. These findings suggest the existence of a public health risk; therefore, there is a need to perform wider and more complete studies to determine the actual situation of Salmonella ssp. egg contamination in the country.

[Evaluation of infectious hematopoietic necrosis, infectious pancreatic necrosis and viral hemorrhagic septicemia viruses in Iranian and imported rainbow trout eggs: a cross sectional study]

Infectious hematopoietic necrosis [IHN], viral hemorrhagic septicemia [VHS] and infectious pancreatic necrosis [IPN] as important viral diseases of salmonids, especially rainbow trout can be led to mass mortality among cultured fish. The aim of the present study was to show if IHN, IPN and VHS viruses can be detected in Iranian and imported rainbow trout eyed eggs and to compare their abundances among the hatcheries of 3 regions [Farsan, Koohrang and Lordegan] in Chaharmahal va Bakhtyari Province. In each area, three hatcheries were selected, 20 eyed eggs were randomly sampled from each farm. The samples were transferred into the sterile tubes and identified by reverse transcriptase -PCR. Meanwhile, physicochemical factors were recorded for each fish. While total infection rate in eggs was 23.3%, the level of infection for IPN, IHN and VHS was 12.5%, 10% and 0.83%, respectively. In this respect, maximum and minimum frequency were observed in Farsan [19.15%] and Koohrang [0.83%]. Comparison of the infected of eggs, based on their origin, showed that the infection rates in Iranian and imported eggs were 20% and 3.33%, respectively. The results revealed that rainbow trout eggs should be considered as major source for transmission of aquatic viruses. Hence, molecular identification of above mentioned viruses in rainbow trout eggs should be done

Establecimiento de una línea celular primaria a partir de huevos con embrión de Toxocara canis / Establishing a primary cell line from Toxocara canis embryonated eggs

Introducción. Toxocara canis es el segundo nematelminto más prevalente en perros a nivel regional y entre los tres más frecuentes en algunos países de la región. Debido a que la fuente de contaminación es el perro, éste se convierte en un nematodo con gran potencial zoonótico. Por esta razón, consideramos importante disponer de una línea celular de este helminto para el estudio de los aspectos básicos, así como para el desarrollo de técnicas diagnósticas. Objetivo. Obtener una línea celular primaria a partir de huevos con embrión de T. canis. Métodos. Los parásitos se extrajeron del intestino delgado de perros menores de un año. Las células embrionarias se obtuvieron mediante la embriogénesis de los huevos de los nematodos adultos, en cuatro diferentes medios; dos ricos en sustancias nutritivas, el tercero con formol al 1 % y el cuarto con agua destilada. Las células se obtuvieron mediante disociación mecánica de los huevos con embrión mediante la utilización de jeringas 30G. Resultados. El tiempo estimado de obtención de la línea celular fue de 15 días, en los que siete eran utilizados en la embriogénesis de los huevos. Las células respondieron positivamente a los métodos de crioconservación luego de dos días, e inclusive dos meses después, permitiendo fases de replicación de cuatro pases. Conclusiones. Se logró obtener una línea celular de T. canis a partir de huevos con embrión de este helminto. Esta línea celular ayudará al entendimiento de las relaciones patógenas, posibles blancos terapéuticos y para el desarrollo de métodos diagnósticos.

Introduction: Toxocara canis is the second most prevalent nemathelminthes in dogs at regional level and among the three most frequent in some countries in the region. Due to the fact that the dog is the contamination source, it becomes a nematode with a high zoonotic potential, so we consider it important to be able to use the cell line of this helminth to study the basic aspects, as well as the development of diagnostic techniques. Objective: To obtain a primary cell line from embryonated eggs of T.canis. Methods: The parasites were extracted from the small intestines of dogs under one year old. Embryonic cells were obtained by embryogenesis of the eggs secreted by adult worms in four different media; two were rich in nutrients, one was 1% formaldehyde, and the other was distilled water. The cells were obtained by mechanical dissociation of embryonated eggs using 30G needles. Results: The estimated time for obtaining the cell line was fifteen days, from which seven were used for egg embryogenesis. The cells responded positively to the cryopreservation methods after two days or even two months, allowing a replication phase with four passes. Conclusions: We managed to obtain a cell line from T. canis embryonated eggs. This cell line will help the understanding of pathogenic relationships, potential therapeutic targets and for developing diagnostic methods.

Detection of avian leukosis virus subgroup J in albumen of commercial and native fowl eggs using RT-PCR in Fars province of Iran

The subgroup J of ALV [ALV-J] has emerged as an important pathogen of meat-type chickens since 1989. This virus is responsible for economic losses due to both mortality and depressed performance in chickens. So, the objective of this study is the detection of ALV-J in the albumen of commercial and native fowl eggs using RT-PCR. Three hundred and seventy egg albumens were randomly selected from different farms of Fars province, Iran. These eggs were obtained from the flocks of two research centers on native fowl production [70 eggs], a broiler grandparent farm [60 eggs], three broiler breeder farms [180 eggs], and a commercial layer flock [60 eggs]. RT-PCR was undertaken on isolated RNA from egg samples using a pair of ALV-J specific primers H5/H7 that produced a 545 basepair fragment. RT-PCR analyses detected ALV-J in 15 of 180 [8.33%] samples from three broiler breeders farms, 17 of 70 [24.28%] samples from flocks of two research centers of native fowls production, and none of the samples of commercial layer and broiler grandparent farms. Direct sequencing using primers specific for subgroup ALV-J verified the viral subgroup in the RT-PCR amplification products. This is the first report of the ALV-J in egg albumen in Iran which indicates the necessity to apply eradication programs for ALV-J in the poultry industry and native fowls in Iran

Detection of avian leukosis virus [ALV] in albumin of Shiraz commercial and local layer flocks using ELISA and RT-PCR

Avian leukosis viruses [ALVs] cause different types of tumours in poultry and can affect the health and egg production of the birds. To investigate the presence of the virus in chicken layer flocks in Shiraz, 222 egg albumen from local layer breeder [25 eggs], local layer grand parent [30 eggs], broiler breeder [60 eggs], commercial layer [46 eggs] and broiler grand parent [61 eggs] were tested by antigen-capture enzyme-linked immunosorbent assay [AC-ELISA]. The results showed that 3.33, 76 and 80% of commercial broiler breeder, local layer breeder and local layer grand parent were positive, respectively. Thirty-five albumen samples were randomly selected and tested by RT-PCR using PU1/PU2 and PA1/PA2 primer sets. The samples with ELISA S/P ratio equal or more than 0.17 were positive by RT-PCR using PA1/PA2 primers. This is the first report of the presence of the ALV in egg albumin samples of chicken layer flocks in Shiraz