ABSTRACT
Escherichia albertii is a recently recognized close relative of Escherichia coli. This emerging enteropathogen possesses a type III secretion system (T3SS) encoded by the locus of enterocyte effacement, similar to enteropathogenic and enterohemorrhagic E. coli (EPEC and EHEC). Shiga toxin-producing strains have also been identified. The genomic features of E. albertii, particularly differences from other Escherichia species, have not yet been well clarified. Here, we sequenced the genome of 29 E. albertii strains (3 complete and 26 draft sequences) isolated from multiple sources and performed intraspecies and intragenus genomic comparisons. The sizes of the E. albertii genomes range from 4.5 to 5.1 Mb, smaller than those of E. coli strains. Intraspecies genomic comparisons identified five phylogroups of E. albertii. Intragenus genomic comparison revealed that the possible core genome of E. albertii comprises 3,250 genes, whereas that of the genus Escherichia comprises 1,345 genes. Our analysis further revealed several unique or notable genetic features of E. albertii, including those responsible for known biochemical features and virulence factors and a possibly active second T3SS known as ETT2 (E. coli T3SS 2) that is inactivated in E. coli. Although this organism has been observed to be nonmotile in vitro, genes for flagellar biosynthesis are fully conserved; chemotaxis-related genes have been selectively deleted. Based on these results, we have developed a nested polymerase chain reaction system to directly detect E. albertii. Our data define the genomic features of E. albertii and provide a valuable basis for future studies of this important emerging enteropathogen.
Subject(s)
Enteropathogenic Escherichia coli/genetics , Genome, Bacterial , Base Sequence , Enteropathogenic Escherichia coli/isolation & purification , Enteropathogenic Escherichia coli/pathogenicity , Gene Transfer, Horizontal , Molecular Sequence Data , Virulence/geneticsABSTRACT
Vibrio parahaemolyticus carrying the tdh gene, encoding the thermostable direct hemolysin (TDH), or the trh gene, encoding the TDH-related hemolysin (TRH), are both considered virulent strains. There are, however, disproportionally fewer reports of infections caused by seafood contaminated with trh-positive strains than by seafood contaminated with tdh-positive strains. Bivalves such as clams and oysters are the major seafood varieties associated with the infections. In this study, the prevalence of strains possessing the tdh and trh genes was investigated in Japan in 74 samples collected in 2007-2008 and in 177 samples collected in 2010 of domestic bivalves, bloody clams, hen clams, short-neck clams, and rock oysters. The tdh-positive and trh-negative, tdh-negative and trh-positive, and tdh-positive and trh-positive samples represented 5.4%, 12.2%, and 4.1% of all samples collected in 2007-2008, and 5.1%, 18.6%, and 5.6% of all samples collected in 2010, respectively. As determined by polymerase chain reaction, the prevalence of tdh negative and trh positive in all samples was two to four times higher than that of tdh positive and trh negative. In the samples collected in 2010, the tdh-negative and trh-positive V. parahaemolyticus (20 samples) was more often isolated than tdh-positive and trh-negative V. parahaemolyticus (7 samples). The most common serotype of tdh-positive isolates (22 of 24 strains) was pandemic O3:K6. The trh-positive isolates (61 strains) were various serotypes including OUT:KUT. In 330 V. parahaemolyticus outbreaks and sporadic infections in Japan, most outbreaks and sporadic infections were caused by tdh-positive and trh-negative strains (89.4%). The frequencies of infections caused by tdh-negative and trh-positive, and both tdh- and trh-positive strains were 1.2% and 3.0%, respectively. This finding suggests that the virulence of trh might be less than that of tdh, although trh-positive V. parahaemolyticus frequently contaminated bivalves.
Subject(s)
Bacterial Proteins/toxicity , Bivalvia/microbiology , Hemolysin Proteins/toxicity , Shellfish Poisoning/etiology , Shellfish/adverse effects , Vibrio parahaemolyticus/pathogenicity , Virulence Factors/analysis , Animals , Arcidae/microbiology , Bacterial Proteins/analysis , Bacterial Proteins/chemistry , Bacterial Toxins/analysis , Bacterial Toxins/chemistry , Bacterial Toxins/toxicity , Crassostrea/microbiology , Disease Outbreaks , Electrophoresis, Gel, Pulsed-Field , Hemolysin Proteins/analysis , Hemolysin Proteins/chemistry , Hot Temperature , Humans , Japan/epidemiology , Molecular Typing , Polymerase Chain Reaction , Protein Stability , Shellfish/analysis , Shellfish/economics , Shellfish/microbiology , Shellfish Poisoning/epidemiology , Shellfish Poisoning/microbiology , Vibrio Infections/epidemiology , Vibrio Infections/microbiology , Vibrio parahaemolyticus/classification , Vibrio parahaemolyticus/growth & development , Vibrio parahaemolyticus/isolation & purification , Virulence , Virulence Factors/chemistrySubject(s)
Caliciviridae Infections/virology , Gastroenteritis/virology , Sapovirus/classification , Sapovirus/genetics , Viral Nonstructural Proteins/genetics , Viral Structural Proteins/genetics , Caliciviridae Infections/epidemiology , Child , Child, Preschool , Cluster Analysis , Gastroenteritis/epidemiology , Humans , Infant , Molecular Epidemiology , Molecular Sequence Data , Phylogeny , RNA, Viral/genetics , Sapovirus/isolation & purification , Sequence Analysis, DNAABSTRACT
More than 27 outbreaks per year of food poisoning caused by consuming horse meat were reported in Kumamoto Prefecture (including Kumamoto City) from January 2009 to September 2011. It was found that the causative agent of the outbreaks was a protein with a molecular weight of 15 kDa that had originated from bradyzoites of Sarcocystis fayeri parasitizing the horse meat. Rabit ileal loop tests showed that pepsin treatment of homogenates of frozen horse meat containing the cysts of S. fayeri induced loss of toxicity, presumably by digestion of the proteinous causative agent(s). Slices of horse meat containing the cysts were frozen at below -20°C for various periods. The cysts were collected after thawing the slices, then treated in an artificial stomach juice containing pepsin. The bradyzoites of the cysts kept at -20°C for 48 hr or more completely disappeared. Simultaneously, the 15 kDa protein also disappeared in the frozen cysts. After notifying the public and recommending freezing treatment of horse meat, no subsequent cases of food poisoning were reported. This indicates that freezing of horse meat is effective to prevent the occurrence of food poisoning caused by consuming raw horse meat containing S. fayeri.
Subject(s)
Food Handling/methods , Foodborne Diseases/prevention & control , Foodborne Diseases/parasitology , Freezing , Meat/poisoning , Meat/parasitology , Sarcocystis/pathogenicity , Sarcocystosis/prevention & control , Sarcocystosis/parasitology , Animals , Foodborne Diseases/epidemiology , Horses , Humans , Japan/epidemiology , Rabbits , Sarcocystis/isolation & purificationABSTRACT
Although Escherichia albertii is an emerging intestinal pathogen, it has been associated only with sporadic human infections. In this study, we determined that a human gastroenteritis outbreak at a restaurant in Japan had E. albertii as the major causative agent.
Subject(s)
Adhesins, Bacterial/genetics , Disease Outbreaks , Enterobacteriaceae Infections/epidemiology , Escherichia coli Proteins/genetics , Escherichia coli/genetics , Escherichia/genetics , Gastroenteritis/epidemiology , Bacterial Typing Techniques , Electrophoresis, Gel, Pulsed-Field , Enterobacteriaceae Infections/microbiology , Escherichia/classification , Escherichia/isolation & purification , Escherichia coli/classification , Escherichia coli/isolation & purification , Food Contamination , Food Microbiology , Gastroenteritis/microbiology , Humans , Japan/epidemiology , Phylogeny , Sequence Analysis, DNAABSTRACT
Sapovirus (SaV) is an important pathogen that causes acute gastroenteritis in humans. Human SaV is highly diverse genetically and is classified into multiple genogroups and genotypes. At present, there is no clear evidence for gastroenteritis cases caused by re-infection with SaV. We found that two individuals were sequentially infected with SaVs of two different genogroups and had gastroenteritis after each infection, although in one of the subsequent cases, both SaV and norovirus were detected. We also found a genetic shift in SaVs from gastroenteritis outpatients in the same geographical location. Our results suggest that protective immunity may be at least genogroup-specific for SaV.