Flow cytometric characterization of Peyer's patch and cecal tonsil T lymphocytes in laying hens following challenge with Salmonella enterica serovar Enteritidis

2010 ◽  
Vol 133 (2-4) ◽  
pp. 276-281 ◽  
Author(s):  
Peter S. Holt ◽  
Lara E. Vaughn ◽  
Richard K. Gast
2014 ◽  
Vol 65 (2) ◽  
pp. 631-637
Author(s):  
Daniel C. Shippy ◽  
Nicholas M. Eakley ◽  
Dareen M. Mikheil ◽  
Anna De La Cotera ◽  
Amin A. Fadl

PLoS ONE ◽  
2012 ◽  
Vol 7 (10) ◽  
pp. e48101 ◽  
Author(s):  
Marta Matulova ◽  
Jana Rajova ◽  
Lenka Vlasatikova ◽  
Jiri Volf ◽  
Hana Stepanova ◽  
...  

2009 ◽  
Vol 58 (1) ◽  
pp. 86-93 ◽  
Author(s):  
N. De Lappe ◽  
G. Doran ◽  
J. O'Connor ◽  
C. O'Hare ◽  
M. Cormican

The 16 Salmonella enterica serovar Enteritidis (S. Enteritidis) typing phages (SETPs) used in the Laboratory of Enteric Pathogens (Health Protection Agency, London, UK) phage-typing scheme have not previously been characterized in detail. We have examined the adsorption properties of the phages with respect to a number of S. enterica serovars and defined phage morphology with electron microscopy. PFGE was used to estimate overall genome size and banding patterns generated by electrophoresis following restriction endonuclease digestion of the genome with HindIII were compared. PCR amplification and sequencing of selected genes was performed. The 16 phages comprise three morphotypes, Podoviridae (SETP1, 8, 10, 14, 15 and 16), Siphoviridae (SETP3, 5, 7, 11, 12 and 13) and Myoviridae (SETP2, 4, 6 and 9). All Podoviridae and Siphoviridae, but not Myoviridae, adsorbed to the O12 lipopolysaccharide antigen of Salmonella serogroups B (4,12) and D1 (9,12). The genome sizes for the Podoviridae and Siphoviridae (PFGE-A) were approximately 42 kb. The genome size for Myoviridae SETP2, 4 and 9 was 36.5 kb, and for myovirus SETP6 was 27 kb. HindIII digestion of phage DNA produced 9 distinct patterns of 8 to 11 bands. Relationships between phages based on digest patterns were consistent with those defined by morphology. The Podoviridae had homologues of several P22 genes while the Siphoviridae had homologues of several genes present in the sequenced siphovirus SETP3 (EF177456). This study represents an initial step in characterizing the molecular basis that underlies the widely used S. Enteritidis typing scheme.


2012 ◽  
Vol 78 (6) ◽  
pp. 1785-1793 ◽  
Author(s):  
L. Farris Hanna ◽  
T. David Matthews ◽  
Elizabeth A. Dinsdale ◽  
David Hasty ◽  
Robert A. Edwards

ABSTRACTPhages are a primary driving force behind the evolution of bacterial pathogens by transferring a variety of virulence genes into their hosts. Similar to other bacterial genomes, theSalmonella entericaserovar Enteritidis LK5 genome contains several regions that are homologous to phages. Although genomic analysis demonstrated the presence of prophages, it was unable to confirm which phage elements within the genome were viable. Genetic markers were used to tag one of the prophages in the genome to allow monitoring of phage induction. Commonly used laboratory strains ofSalmonellawere resistant to phage infection, and therefore a rapid screen was developed to identify susceptible hosts. This approach showed that a genetically tagged prophage, ELPhiS (Enteritidis lysogenic phage S), was capable of infectingSalmonellaserovars that are diverse in host range and virulence and has the potential to laterally transfer genes between these serovars via lysogenic conversion. The rapid screen approach is adaptable to any system with a large collection of isolates and may be used to test the viability of prophages found by sequencing the genomes of various bacterial pathogens.


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