Isolation of Mycoplasma spp. from Geese with Pneumonia and Identification of Microbial Isolates via Molecular Methods

This study aimed to investigate Mycoplasma species in the lungs of 500 geese with pneumonia from the Kars region (Turkey) via cultural and molecular methods. The samples were cultured on Freys Broth and Agar media. To identify Mycoplasma species a Growth Inhibition Test was used. The identification was continued with species-specific PCR and sequence analysis which provide amplification of the genes dnaX, pcrA, rpoB, and the sequence of the 16S rRNA gene, respectively. In addition, Mycoplasma gallisepticum and Mycoplasma synoviae from pneumonic lung samples were directly analyzed via Multiplex Real-time PCR. As a result, 51 Mycoplasma strains were isolated and 32 were identified as Mycoplasma anatis, 9 as Mycoplasma anseris, 5 as Mycoplasma cloacale and 3 as Mycoplasma anserisalpingitis. Two Mycoplasma isolates that could not be identified were grouped in the same branch as a result of 16S RNA sequencing and their nearest neighbour was found to be Mycoplasma sp. 2045 (GenBankNo.MK615061.1). M. gallisepticum DNA was detected in 3 pneumonic lung samples and M. gallisepticum/M. synoviae DNAs were found simultaneously in 1 sample. While some Mycoplasma species identified in this study consolidated their place as pneumonic agents, some increased their potential to become a pneumonic agent when compared with cases caused by well-recognized Mycoplasma strains. Two isolates were identified as -Mycoplasma spp. as their 16S rRNA gene sequence identity levels scored below the threshold of 98.7% for species demarcation and still need to be defined whether they are possible representatives of a novel Mycoplasma species.(AU)

Isolation of Mycoplasma spp. from Geese with Pneumonia and Identification of Microbial Isolates via Molecular Methods

This study aimed to investigate Mycoplasma species in the lungs of 500 geese with pneumonia from the Kars region (Turkey) via cultural and molecular methods. The samples were cultured on Frey’s Broth and Agar media. To identify Mycoplasma species a Growth Inhibition Test was used. The identification was continued with species-specific PCR and sequence analysis which provide amplification of the genes dnaX, pcrA, rpoB, and the sequence of the 16S rRNA gene, respectively. In addition, Mycoplasma gallisepticum and Mycoplasma synoviae from pneumonic lung samples were directly analyzed via Multiplex Real-time PCR. As a result, 51 Mycoplasma strains were isolated and 32 were identified as Mycoplasma anatis, 9 as Mycoplasma anseris, 5 as Mycoplasma cloacale and 3 as Mycoplasma anserisalpingitis. Two Mycoplasma isolates that could not be identified were grouped in the same branch as a result of 16S RNA sequencing and their nearest neighbour was found to be Mycoplasma sp. 2045 (GenBankNo.MK615061.1). M. gallisepticum DNA was detected in 3 pneumonic lung samples and M. gallisepticum/M. synoviae DNAs were found simultaneously in 1 sample. While some Mycoplasma species identified in this study consolidated their place as pneumonic agents, some increased their potential to become a pneumonic agent when compared with cases caused by well-recognized Mycoplasma strains. Two isolates were identified as -Mycoplasma spp. as their 16S rRNA gene sequence identity levels scored below the threshold of 98.7% for species demarcation and still need to be defined whether they are possible representatives of a novel Mycoplasma species.

Effects of culture medium and substrate on attachment of in vitro produced bovine embryos

The study of large animal embryonic stem cells (ESCs) in vitro has implications for the understanding of lineage differentiation and transgenesis. The first step for ESC derivation is the attachment of the embryo to a substrate on which they can form outgrowths. However, the culture conditions for large animal embryo attachment and ESC derivation have not been studied extensively. Defining culture conditions for embryo attachment such as culture medium and substrate is an important first step for derivation of inner cell mass-derived stem cells. The aim of this study was to compare different types of culture media and substrates for their ability to support attachment of in vitro produced bovine embryos in culture. Bovine embryos were produced in vivo following established protocols. Blastocysts formed on day 8 after fertilization were transferred to 12-well culture plates containing different types of culture media (Dulbecco's Modified Eagle Medium, DMEM or Medium 199, M199) and substrates [bovine fetal fibroblasts, goat fetal fibroblasts, mouse embryonic fibroblasts (STO) or non-cellular substrates (gelatin, laminin, fibronectin)]. Percentage of attached embryos and number of days since fertilization required for attachment were recorded. Bovine blastocysts preferrably attached to feeder cells rather than non-cellular substrates and there was an interact ion of feeder cell type and culture medium used. Therefore, the choice of both feeder cell type and culture medium has to be considered when optimizing conditions to derive cell lines from bovine embryos.

Effects of culture medium and substrate on attachment of in vitro produced bovine embryos

The study of large animal embryonic stem cells (ESCs) in vitro has implications for the understanding of lineage differentiation and transgenesis. The first step for ESC derivation is the attachment of the embryo to a substrate on which they can form outgrowths. However, the culture conditions for large animal embryo attachment and ESC derivation have not been studied extensively. Defining culture conditions for embryo attachment such as culture medium and substrate is an important first step for derivation of inner cell mass-derived stem cells. The aim of this study was to compare different types of culture media and substrates for their ability to support attachment of in vitro produced bovine embryos in culture. Bovine embryos were produced in vivo following established protocols. Blastocysts formed on day 8 after fertilization were transferred to 12-well culture plates containing different types of culture media (Dulbecco's Modified Eagle Medium, DMEM or Medium 199, M199) and substrates [bovine fetal fibroblasts, goat fetal fibroblasts, mouse embryonic fibroblasts (STO) or non-cellular substrates (gelatin, laminin, fibronectin)]. Percentage of attached embryos and number of days since fertilization required for attachment were recorded. Bovine blastocysts preferrably attached to feeder cells rather than non-cellular substrates and there was an interact ion of feeder cell type and culture medium used. Therefore, the choice of both feeder cell type and culture medium has to be considered when optimizing conditions to derive cell lines from bovine embryos.(AU)