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1.
Food Chem ; 413: 135553, 2023 Jul 01.
Article in English | MEDLINE | ID: mdl-36745944

ABSTRACT

Inspired by a biomineralization behavior, we prepared a nanoflower-like artificial clickase (namely LCN clickase) for portable and sensitive click SERS immunoassay of foodborne bacterial pathogen. Encouraged by its high click catalytic activity to trigger Cu(I)-catalyzed azide-alkyne cycloaddition reaction, LCN clickase was successfully used for establishing a novel click SERS immunoassay by combining the clickase-mediated SERS signal variation at Raman-silent region. The developed method not only effectively eliminated the interferences between Raman reporter and biological species, but also reduced the complex sample matrix interference. Compared with traditional CuAAC-based immunoassays, the established method avoided the superfluous dissolution process of nanocatalysts and eliminated the requirement of reducing agent during detection, thereby shortening detection time and improving detection reliability. Impressively, the proposed method showed high selectivity and sensitivity for detection of Salmonella enterica serovar Paratyphi B with a low LOD of 20 CFU/mL, exhibiting a great potential in detection of foodborne bacterial pathogen in food samples.


Subject(s)
Bacteria , Salmonella paratyphi B , Reproducibility of Results , Immunoassay/methods , Spectrum Analysis, Raman/methods
2.
Microb Genom ; 9(2)2023 02.
Article in English | MEDLINE | ID: mdl-36825878

ABSTRACT

Salmonella Paratyphi B infections in England are the least common imported typhoidal infection but can still cause invasive disease. Sentinel surveillance at the reference laboratory detected an outbreak from Iraq due to reported travel history, enabling enhanced PCR testing for a quick diagnosis.


Subject(s)
Paratyphoid Fever , Salmonella paratyphi B , Humans , Salmonella paratyphi B/genetics , Paratyphoid Fever/epidemiology , Sentinel Surveillance , Iraq , Mass Gatherings , Genomics , Disease Outbreaks
4.
Paediatr Int Child Health ; 42(3-4): 157-160, 2022.
Article in English | MEDLINE | ID: mdl-36739546

ABSTRACT

A 3-month-old female infant with meningo-encephalitis caused by Salmonella enterica Paratyphi B var. Java is described. The aetiological agent was confirmed in six CSF samples; however, none of the blood or faecal samples was positive for the same pathogen. The presence of the bacteria was confirmed in the CSF by culture, serology and Multiplex PCR assay. The infant developed dilated subarachnoid spaces and right-sided hemiparesis associated with the persistent bacterial meningo-encephalitis. She was re-admitted 2 weeks after recovery and initial discharge from hospital owing to recurrence of S. enterica Paratyphi B bacteria in the CSF and the development of large bilateral subdural effusions in the brain. Computed tomography and the clinical course confirmed dynamically progressive meningo-encephalitis. Following further parenteral antibiotics and symptomatic treatment, the child's condition improved. After a total of 24 days in the PICU, she was sufficiently improved to be discharged with a residual right-sided hemiparesis. However, sadly she died a week after discharge.Abbreviation: ALT: alanine aminotransferase; API: analytical profile index 20 E-test; AST: aspartate aminotransferase; CRP: C-reactive protein; CSF: cerebrospinal fluid; CT: computed tomography; EUCAST: European Committee on Antimicrobial Susceptibility Testing; MDCT: multi-detector computed tomography; PCR: polymerase chain reaction; PICU: paediatric intensive care unit; RBC: red blood cells; VITEK: automated instrument for identification/antimicrobial susceptibility testing; WBC: white blood cells.


Subject(s)
Encephalitis , Meningitis , Subdural Effusion , Child , Humans , Infant , Female , Salmonella paratyphi B , Dilatation , Indonesia , Anti-Bacterial Agents/therapeutic use , Subarachnoid Space
6.
Pediatr Infect Dis J ; 40(10): e374-e378, 2021 10 01.
Article in English | MEDLINE | ID: mdl-34321443

ABSTRACT

BACKGROUND: Salmonella Paratyphi B (Paratyphoid B) is a rare infection and a notifiable disease in England. Disease is typically mild, and chronic carriage in children has been described in endemic countries. Almost all cases in England are imported, with very few cases of community transmission reported. METHODS: The aim of this work was to describe an unusual cluster of Paratyphoid B cases transmitted within England, examining clinical, epidemiologic and microbiologic data. Detailed phylogenetic analysis is presented to corroborate public health epidemiologic links between cases. RESULTS: One child had recently returned from an endemic area and had mild gastrointestinal symptoms. One year later, 2 other children with no travel history developed invasive disease requiring hospitalization. Epidemiologic links confirmed person-to-person spread between these three cases. All isolates of S. Paratyphi B (n = 93) received by the Gastrointestinal Bacteria Reference Unit between 2014 and 2019 were typed using whole genome sequencing. Three cases of Paratyphoid B were identified in the same geographical location over a 2-year period. S. Paratyphi B strains isolated from the stool and blood of the three cases were closely linked (0-5 single-nucleotide polymorphisms) using whole genome sequencing. CONCLUSIONS: This case series highlights the potential public health risks of paratyphoid B and the range of pediatric complications associated with this illness, especially in younger children. Although rare, chronic carriage of Paratyphoid B can lead to transmission in nonendemic areas and should be considered in all children presenting with signs of enteric fever even where there is no history of foreign travel.


Subject(s)
Carrier State/drug therapy , Carrier State/microbiology , Paratyphoid Fever/drug therapy , Public Health/standards , Salmonella paratyphi B/genetics , Child, Preschool , England/epidemiology , Female , Humans , Male , Paratyphoid Fever/epidemiology , Paratyphoid Fever/microbiology , Parents , Phylogeny , Risk Factors , Salmonella paratyphi B/drug effects , Salmonella paratyphi B/physiology , Travel , Whole Genome Sequencing
7.
FEMS Microbiol Lett ; 368(7)2021 04 25.
Article in English | MEDLINE | ID: mdl-33830213

ABSTRACT

Salmonellosis is an important worldwide food-borne disease. Increasing resistance to Salmonella spp. has been reported in recent years, and now the prevalence of multidrug-resistant Salmonella spp. is a worldwide problem. This necessitates alternative approaches like phage therapy. This study aimed to isolate bacteriophages specific for Salmonella enterica serovar Paratyphi B and S. enterica serovar Typhimurium isolated from different sources (chicken meat, beef and eggshells). The antibiotic resistance profiles of the bacteria were determined by phenotypic and genotypic methods. The prevalence of extended-spectrum ß-lactamase genes was examined by polymerase chain reaction. In total, 75% of the isolated Salmonella strains were resistant to tetracycline, whereas 70% of them were resistant to azithromycin. All of the isolates from beef were resistant to nalidixic acid. The most common extended-spectrum ß-lactamase genes among the isolates were blaSHV (15%) followed by blaTEM (10%) and blaCTX (5%). Two specific bacteriophages were isolated and characterized. The host range for vB_SparS-ui was Salmonella Paratyphi B, S. enterica serovar Paratyphi A and S. enterica, while that for vB_StyS-sam phage was Salmonella Typhimurium and S. enterica serovar Enteritidis. The characteristics of the isolated phages indicate that they are proper candidates to be used to control some foodstuff contaminations and also phage therapy of infected animals.


Subject(s)
Salmonella Phages/isolation & purification , Salmonella Phages/physiology , Salmonella paratyphi B/virology , Salmonella typhimurium/virology , Anti-Bacterial Agents/pharmacology , Bacterial Proteins/genetics , Drug Resistance, Bacterial/genetics , Genome, Viral/genetics , Host Specificity , Hydrogen-Ion Concentration , Salmonella Phages/ultrastructure , Salmonella enterica/drug effects , Salmonella enterica/genetics , Salmonella enterica/virology , Salmonella paratyphi B/drug effects , Salmonella paratyphi B/genetics , Salmonella typhimurium/drug effects , Salmonella typhimurium/genetics , Serogroup , Sodium Chloride , Temperature , Viral Proteins/chemistry , Viral Proteins/genetics
9.
Am J Trop Med Hyg ; 103(1): 231-233, 2020 07.
Article in English | MEDLINE | ID: mdl-32458786

ABSTRACT

Paratyphoid fever is one of the major causes of morbidity of febrile illnesses in endemic regions. We report a case of high-grade fever in an infant who was positive for Salmonella enterica serovar Paratyphi B (S. Paratyphi B) both in blood and stool cultures. The baby was enrolled in the passive surveillance of multicenter, multicomponent epidemiological study of enteric fever (Strategic Typhoid alliance across Africa and Asia; STRATAA) conducted in a population of 110,000 residents over 2 years in an urban slum, Dhaka, Bangladesh. This is the only patient who was positive for S. Paratyphi B in blood and stool among more than 6,000 febrile ill patients enrolled in the passive surveillance. The report shows the significance of surveillance to identify changes in the epidemiology of enteric fever.


Subject(s)
Paratyphoid Fever/diagnosis , Population Surveillance/methods , Salmonella paratyphi B , Bangladesh/epidemiology , Female , Fever/etiology , Humans , Infant , Paratyphoid Fever/epidemiology , Paratyphoid Fever/microbiology , Poverty Areas
10.
Emerg Infect Dis ; 26(6): 1164-1173, 2020 06.
Article in English | MEDLINE | ID: mdl-32441616

ABSTRACT

Salmonella enterica serovar Paratyphi B variant Java sequence type 28 is prevalent in poultry and poultry meat. We investigated the evolutionary relatedness between sequence type 28 strains from Europe and Latin America using time-resolved phylogeny and principal component analysis. We sequenced isolates from Colombia, Guatemala, Costa Rica, and the Netherlands and complemented them with publicly available genomes from Europe, Africa, and the Middle East. Phylogenetic time trees and effective population sizes (Ne) showed separate clustering of strains from Latin America and Europe. The separation is estimated to have occurred during the 1980s. Ne of strains increased sharply in Europe around 1995 and in Latin America around 2005. Principal component analysis on noncore genes showed a clear distinction between strains from Europe and Latin America, whereas the plasmid gene content was similar. Regardless of the evolutionary separation, similar features of resistance to ß-lactams and quinolones/fluoroquinolones indicated parallel evolution of antimicrobial resistance in both regions.


Subject(s)
Salmonella enterica , Salmonella paratyphi B , Africa , Animals , Anti-Bacterial Agents/pharmacology , Colombia , Costa Rica , Drug Resistance, Bacterial , Drug Resistance, Multiple, Bacterial , Europe/epidemiology , Guatemala , Indonesia , Latin America/epidemiology , Middle East , Netherlands , Phylogeny , Poultry , Salmonella enterica/genetics , Salmonella paratyphi B/genetics
11.
PLoS Negl Trop Dis ; 13(8): e0007650, 2019 08.
Article in English | MEDLINE | ID: mdl-31412039

ABSTRACT

Enteric fevers, caused by the Salmonella enterica serovars Typhi (ST), Paratyphi A (PA) and Paratyphi B (PB), are life-threatening illnesses exhibiting very similar clinical symptoms but with distinct epidemiologies, geographical distributions and susceptibilities to antimicrobial treatment. Nevertheless, the mechanisms by which the host recognizes pathogens with high levels of homology, such as these bacterial serovars, remain poorly understood. Using a three-dimensional organotypic model of the human intestinal mucosa and PA, PB, and ST, we observed significant differences in the secretion patterns of pro-inflammatory cytokines and chemokines elicited by these serovars. These cytokines/chemokines were likely to be co-regulated and influenced the function of epithelial cells, such as the production of IL-8. We also found differing levels of polymorphonuclear leukocyte (PMN) migration among various infection conditions that either included or excluded lymphocytes and macrophages (Mϕ), strongly suggesting feedback mechanisms among these cells. Blocking experiments showed that IL-1ß, IL-6, IL-8, TNF-α and CCL3 cytokines were involved in the differential regulation of migration patterns. We conclude that the crosstalk among the lymphocytes, Mϕ, PMN and epithelial cells is cytokine/chemokine-dependent and bacterial-serotype specific, and plays a pivotal role in orchestrating the functional efficiency of the innate cells and migratory characteristics of the leukocytes.


Subject(s)
Cell Communication , Leukocytes/immunology , Salmonella paratyphi A/immunology , Salmonella paratyphi B/immunology , Salmonella typhi/immunology , Typhoid Fever/immunology , Cell Movement , Cytokines/analysis , Epithelial Cells/immunology , Humans , Intestinal Mucosa/immunology , Lymphocytes/immunology , Macrophages/immunology , Models, Theoretical , Organ Culture Techniques
12.
Appl Microbiol Biotechnol ; 103(12): 4987-4996, 2019 Jun.
Article in English | MEDLINE | ID: mdl-31062054

ABSTRACT

Discriminating between D-tartrate fermenting and non-fermenting strains of Salmonella enterica subsp. enterica serotype Paratyphi B is of major importance as these two variants have different pathogenic profiles. While D-tartrate non-fermenting S. Paratyphi B isolates are the causative agent of typhoid-like fever, D-tartrate fermenting isolates (also called variant Java) of the same serotype trigger the less dangerous gastroenteritis. The determination of S. Paratyphi B variants requires a time-consuming process and complex biochemical tests. Therefore, a quadruplex real-time PCR method, based on the allelic discrimination of molecular markers selected from the scientific literature and from whole genome sequencing data produced in-house, was developed in this study, to be applied to Salmonella isolates. This method was validated with the analysis of 178 S. Paratyphi B (D-tartrate fermenting and non-fermenting) and other serotypes reaching an accuracy, compared with the classical methods, of 98% for serotyping by slide agglutination and 100% for replacement of the biochemical test. The developed real-time PCR permits to save time and to obtain an accurate identification of a S. Paratyphi B serotype and its D-tartrate fermenting profile, which is needed in routine laboratories for fast and efficient diagnostics.


Subject(s)
Bacterial Typing Techniques , Genotyping Techniques , Real-Time Polymerase Chain Reaction/methods , Salmonella paratyphi B/classification , Anti-Bacterial Agents/pharmacology , Drug Resistance, Multiple, Bacterial , Fermentation , Genetic Variation , Humans , Indonesia , Microbial Sensitivity Tests , Reproducibility of Results , Salmonella paratyphi B/drug effects , Tartrates/metabolism , Whole Genome Sequencing
13.
Int J Food Microbiol ; 290: 180-183, 2019 Feb 02.
Article in English | MEDLINE | ID: mdl-30342248

ABSTRACT

Salmonella enterica serovar Paratyphi B (S. Paratyphi B) is a major foodborne pathogen distributed all over the world. However, little is known about the antibiotic resistance, genetic relatedness and virulence profile of S. Paratyphi B isolated from leafy vegetables and the processing environment in Malaysia. In this study, 6 S. Paratyphi B isolates were recovered from different vegetables and drain water of processing areas obtained from fresh food markets in Malaysia. The isolates were characterized by antibiogram, Pulsed-field gel electrophoresis (PFGE) and virulence genes. Antibiotic susceptibility test showed that 3 of the isolates were resistant to the antibiotics. These include S. Paratyphi B SP251 isolate, which was resistant to chloramphenicol, ampicillin, sulfonamides and streptomycin; Isolate SP246 which was resistant to chloramphenicol, sulfonamides and streptomycin and Isolate SP235 showing resistance to nalidixic acid only. PFGE subtyped the 6 S. Paratyphi B isolates into 6 distinct XbaI-pulsotypes, with a wide range of genetic similarity (0.55 to 0.9). The isolates from different sources and fresh food markets location were genetically diverse. Thirteen (tolC, orgA, spaN, prgH, sipB, invA, pefA, sofB, msgA, cdtB, pagC, spiA and spvB) out of the 17 virulence genes tested were found in all of the S. Paratyphi B isolates. Another gene (lpfC), was found only in one isolate (SP051). None of the isolates possessed sifA, sitC and ironN genes. In summary, this study provides unique information on antibiotic resistance, genetic relatedness, and virulotyping of S. Paratyphi B isolated from leafy vegetables and processing environment.


Subject(s)
Genetic Variation , Salmonella paratyphi B/drug effects , Salmonella paratyphi B/genetics , Vegetables/microbiology , Anti-Bacterial Agents/pharmacology , Drug Resistance, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , Food-Processing Industry , Genes, Bacterial/genetics , Humans , Malaysia , Microbial Sensitivity Tests , Molecular Typing , Salmonella enterica/isolation & purification , Salmonella paratyphi B/virology , Virulence/genetics
14.
mSphere ; 3(6)2018 11 28.
Article in English | MEDLINE | ID: mdl-30487152

ABSTRACT

Enteric fever is caused by three Salmonella enterica serovars: Typhi, Paratyphi A, and Paratyphi B sensu stricto Although vaccines against two of these serovars are licensed (Typhi) or in clinical development (Paratyphi A), as yet there are no candidates for S. Paratyphi B. To gain genomic insight into these serovars, we sequenced 38 enteric fever-associated strains from Chile and compared these with reference genomes. Each of the serovars was separated genomically based on the core genome. Genomic comparisons identified loci that were aberrant between serovars Paratyphi B sensu stricto and Paratyphi B Java, which is typically associated with gastroenteritis; however, the majority of these were annotated as hypothetical or phage related and thus were not ideal vaccine candidates. With the genomic information in hand, we engineered a live attenuated S. Paratyphi B sensu stricto vaccine strain, CVD 2005, which was capable of protecting mice from both homologous challenge and heterologous challenge with S. Paratyphi B Java. These findings extend our understanding of S. Paratyphi B and provide a viable vaccine option for inclusion in a trivalent live attenuated enteric fever vaccine formulation.IMPORTANCE We developed a live attenuated Salmonella enterica serovar Paratyphi B vaccine that conferred protection in mice against challenge with S Paratyphi B sensu stricto and S Paratyphi B Java, which are the causes of enteric fever and gastroenteritis, respectively. Currently, the incidence of invasive S. Paratyphi B sensu stricto infections is low; however, the development of new conjugate vaccines against other enteric fever serovars could lead to the emergence of S. Paratyphi B to fill the niche left by these other pathogens. As such, an effective S. Paratyphi B vaccine would be a useful tool in the armamentarium against Salmonella infections. Comparative genomics confirmed the serovar-specific groupings of these isolates and revealed that there are a limited number of genetic differences between the sensu stricto and Java strains, which are mostly hypothetical and phage-encoded proteins. The observed level of genomic similarity likely explains why we observe some cross-protection.


Subject(s)
Paratyphoid Fever/prevention & control , Salmonella paratyphi B/immunology , Typhoid-Paratyphoid Vaccines/immunology , Animals , Chile , Disease Models, Animal , Mice , Salmonella paratyphi B/genetics , Salmonella paratyphi B/pathogenicity , Survival Analysis , Treatment Outcome , Typhoid-Paratyphoid Vaccines/administration & dosage , Typhoid-Paratyphoid Vaccines/genetics , Typhoid-Paratyphoid Vaccines/isolation & purification , Vaccines, Attenuated/administration & dosage , Vaccines, Attenuated/genetics , Vaccines, Attenuated/immunology , Vaccines, Attenuated/isolation & purification , Whole Genome Sequencing
15.
Epidemiol Infect ; 147: e20, 2018 10 08.
Article in English | MEDLINE | ID: mdl-30293540

ABSTRACT

A cluster of Salmonella Paratyphi B variant L(+) tartrate(+) infections with indistinguishable pulsed-field gel electrophoresis patterns was detected in October 2015. Interviews initially identified nut butters, kale, kombucha, chia seeds and nutrition bars as common exposures. Epidemiologic, environmental and traceback investigations were conducted. Thirteen ill people infected with the outbreak strain were identified in 10 states with illness onset during 18 July-22 November 2015. Eight of 10 (80%) ill people reported eating Brand A raw sprouted nut butters. Brand A conducted a voluntary recall. Raw sprouted nut butters are a novel outbreak vehicle, though contaminated raw nuts, nut butters and sprouted seeds have all caused outbreaks previously. Firms producing raw sprouted products, including nut butters, should consider a kill step to reduce the risk of contamination. People at greater risk for foodborne illness may wish to consider avoiding raw products containing raw sprouted ingredients.


Subject(s)
Disease Outbreaks , Salmonella Food Poisoning/epidemiology , Salmonella paratyphi B/pathogenicity , Seedlings/adverse effects , Vegetable Products/adverse effects , Adolescent , Adult , Age Distribution , Databases, Factual , Female , Food Safety , Humans , Incidence , Male , Middle Aged , Retrospective Studies , Risk Assessment , Salmonella Food Poisoning/etiology , Salmonella Food Poisoning/physiopathology , Sex Distribution , United States/epidemiology
18.
Epidemiol Infect ; 146(11): 1461-1467, 2018 08.
Article in English | MEDLINE | ID: mdl-29880080

ABSTRACT

Foodborne non-typhoidal salmonellosis causes approximately 1 million illnesses annually in the USA. In April 2015, we investigated a multistate outbreak of 65 Salmonella Paratyphi B variant L(+) tartrate(+) infections associated with frozen raw tuna imported from Indonesia, which was consumed raw in sushi. Forty-six (92%) of 50 case-patients interviewed ate sushi during the week before illness onset, and 44 (98%) of 45 who specified ate sushi containing raw tuna. Two outbreak strains were isolated from the samples of frozen raw tuna. Traceback identified a single importer as a common source of tuna consumed by case-patients; this importer issued three voluntary recalls of tuna sourced from one Indonesian processor. Four Salmonella Weltevreden infections were also linked to this outbreak. Whole-genome sequencing was useful in establishing a link between Salmonella isolated from ill people and tuna. This outbreak highlights the continuing foodborne illness risk associated with raw seafood consumption, the importance of processing seafood in a manner that minimises contamination with pathogenic microorganisms and the continuing need to ensure imported foods are safe to eat. People at higher risk for foodborne illness should not consume undercooked animal products, such as raw seafood.


Subject(s)
Disease Outbreaks , Food Microbiology , Paratyphoid Fever/etiology , Raw Foods/microbiology , Salmonella paratyphi B/isolation & purification , Tuna/microbiology , Adolescent , Adult , Aged , Aged, 80 and over , Animals , Child , Child, Preschool , Electrophoresis, Gel, Pulsed-Field , Female , Frozen Foods/adverse effects , Frozen Foods/microbiology , Humans , Indonesia , Infant , Male , Middle Aged , Paratyphoid Fever/epidemiology , Raw Foods/adverse effects , Salmonella paratyphi B/classification , Seafood/adverse effects , Seafood/microbiology , Serotyping , Surveys and Questionnaires , United States/epidemiology , Whole Genome Sequencing , Young Adult
20.
Childs Nerv Syst ; 34(11): 2317-2320, 2018 11.
Article in English | MEDLINE | ID: mdl-29748704

ABSTRACT

Intracranial infection due to Salmonella is uncommon in children. Subdural empyema (SDE) is described with Salmonella typhi as a complication of meningitis. We report a 6-month-old infant with SDE secondary to Salmonella paratyphi B who had presented with prolonged fever and enlarging head. A literature review of Salmonella SDE in infants with respect to clinical course and outcome is presented.


Subject(s)
Empyema, Subdural/microbiology , Paratyphoid Fever/complications , Humans , Infant , Male , Salmonella paratyphi B
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