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1.
Arch Pediatr ; 21 Suppl 2: S62-8, 2014 Nov.
Article in French | MEDLINE | ID: mdl-25456682

ABSTRACT

Group A Streptococcus (GAS) is a human pathogen responsible for a wide range of clinical manifestations. An increase of GAS invasive infections has been described since the mid 1980s. To study the French epidemiology of invasive infections (i) we characterized all GAS invasive strains received at the French National Reference Center for streptococci (CNR-Strep) between 2007 and 2011; (ii) we analyzed the epidemiological data on the corresponding strains. For each strain, emm genotype, superantigen genes and antibiotics susceptibility were determined. Among the 2 603 non redundant invasive GAS strains, 65.1 % (n=1 695) were isolated from blood culture. A streptococcal toxic shock syndrome (STSS) was described in 16.4 % (n=428) of cases, mostly associated with necrotizing fasciitis (NF), pleuropulmonary or osteoarticular infections (p ≤0.001). The case fatality rate was 10.6 %. A total of 102 different emm genotypes were identified. Three emm genotypes predominated, reaching nearly 60 % of the strains: emm 1 (26.7 %), emm 28 (16.4 %), and emm 89 (12.8 %). The proportion of each emm genotype varied according to the year and the age of patients. Among those < 15 years old, the three main genotypes were emm 1 (36.8 %), emm 12 (12.9 %) and emm 4 (9.5 %). The distribution of superantigen genes (SpeA, SpeC and Ssa) was restricted to several emm genotypes. Between 2007 and 2011, the rate of macrolides resistant GAS strains decreased from 7.8 to 5.5 %. emm 1 strains are still the most common especially in most severe clinical manifestations including STSS and NF.


Subject(s)
Streptococcal Infections/epidemiology , Streptococcus pyogenes/isolation & purification , Adolescent , Adult , Age Distribution , Aged , Aged, 80 and over , Anti-Bacterial Agents/pharmacology , Child , Child, Preschool , Fasciitis, Necrotizing/epidemiology , Fasciitis, Necrotizing/microbiology , Female , France/epidemiology , Genotype , Humans , Infant , Infant, Newborn , Male , Microbial Sensitivity Tests , Middle Aged , Pleuropneumonia/epidemiology , Pleuropneumonia/microbiology , Shock, Septic/epidemiology , Shock, Septic/microbiology , Streptococcal Infections/drug therapy , Streptococcus pyogenes/genetics , Young Adult
2.
Arch Pediatr ; 21 Suppl 2: S73-7, 2014 Nov.
Article in French | MEDLINE | ID: mdl-25456684

ABSTRACT

In industrialized countries, group A streptococcal infections were a source of concern, mainly due to the occurrence of rheumatic fever and its cardiac complications. At present, the incidence of rheumatic fever is decreasing in these countries, giving way to an increasing occurrence of invasive streptococcal group A infections with high level of morbidity and mortality. Streptococcal necrotizing fasciitis, a specific entity, emerged these last decades, often in association with chickenpox. The introduction of the varicella vaccine in the province of Quebec routine immunization program, was followed by a significant decrease in the number of necrotizing fasciitis or other skin and soft-tissues infections in our pediatric population. However, in our experience at the CHU Sainte-Justine, this immunization program has not been helpful to reduce the overall incidence of invasive group A streptococcal infections. Conversely, an increase in the number of pleuro-pulmonary and osteo-articular infections was observed.


Subject(s)
Chickenpox Vaccine , Streptococcal Infections/epidemiology , Streptococcus pyogenes , Canada/epidemiology , Chickenpox/epidemiology , Developed Countries , Fasciitis, Necrotizing/epidemiology , Fasciitis, Necrotizing/microbiology , Genotype , Humans , Incidence , Middle Aged , Skin Diseases, Bacterial/epidemiology , Skin Diseases, Bacterial/microbiology , Soft Tissue Infections/epidemiology , Soft Tissue Infections/microbiology , Streptococcus pyogenes/genetics
3.
Clin Microbiol Infect ; 20(12): O1035-41, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24979689

ABSTRACT

In order to improve knowledge on Escherichia coli bacteraemia during pregnancy, we studied clinical data and performed molecular characterization of strains for 29 E. coli bacteraemia occurring in pregnant women. Bacteraemia mostly occurred in the third trimester of pregnancy (45%) and was community-acquired (79%). Portals of entry were urinary (55%) and genital (45%). E. coli strains belonged mainly to phylogroups B2 (72%) and D (17%). Four clonal lineages (i.e. sequence type complex (STc) 73, STc95, STc12 and STc69) represented 65% of the strains. The strains exhibited a high number of virulence factor coding genes (10 (3-16)). Six foetuses died (27%), five of them due to bacteraemia of genital origin (83%). Foetal deaths occurred despite adequate antibiotic regimens. Strains associated with foetal mortality had fewer virulence factors (8 (6-10)) than strains involved in no foetal mortality (11 (4-12)) (p 0.02). When comparing E. coli strains involved in bacteraemia with a urinary portal of entry in non-immunocompromised pregnant vs. non-immunocompromised non-pregnant women from the COLIBAFI study, there was no significant difference of phylogroups and virulence factor coding genes. These results show that E. coli bacteraemia in pregnant women involve few highly virulent clones but that severity, represented by foetal death, is mainly related to bacteraemia of genital origin.


Subject(s)
Bacteremia/complications , Escherichia coli Infections/complications , Escherichia coli Infections/microbiology , Fetal Death/etiology , Pregnancy Complications, Infectious/microbiology , Adolescent , Adult , Community-Acquired Infections/complications , Community-Acquired Infections/microbiology , Escherichia coli/classification , Escherichia coli/genetics , Escherichia coli/isolation & purification , Female , Genotype , Humans , Middle Aged , Pregnancy , Retrospective Studies , Survival Analysis , Virulence Factors/genetics , Young Adult
4.
Arch Pediatr ; 21(7): 736-44, 2014 Jul.
Article in French | MEDLINE | ID: mdl-24938915

ABSTRACT

BACKGROUND: For the past 20 years, three vaccines against the three main bacterial species implicated in meningitis in children have been included in the French vaccine calendar: Haemophilus influenzae b in 1993, 7-valent pneumococcal conjugate vaccine (PCV7) in 2003 (replaced by 13-valent in 2010) and Neisseria meningitidis C in 2009. The French active surveillance network from the GPIP/ACTIV monitors the change in the epidemiological, clinical, and biological features of bacterial meningitis due to vaccine use. METHODS: Over a 12-year period, 233 pediatric wards working with 168 microbiology departments throughout France were asked to report all cases of bacterial meningitis. RESULTS: From January 2001 to December 2012, 4808 bacterial meningitis cases were reported. Between 2001 and 2012, the number of pneumococcal meningitis (PM) cases decreased by 23.4%, and by 32.2% for children less than 2 years old. During this period, the proportion of cases attributable to PCV7 and six additional PCV13 types decreased from 63.3% to 8.1% and 83.7% to 32.4%, respectively. In 2012, the main vaccine types (accounting for 25.8% of cases) were 7F (12.2%), 19A (6.8%), and 19F (6.8%), and the most frequent non-vaccine types were 12F (14.9%), 24F (14.9%), 15B/C (6.8%), 22F (6.8%), and 10A (5.4%). In 2012, the rate of strains with decreased susceptibility to cefotaxime/ceftriaxone (MIC>0.5 µg/mL) represented less than 3% of cases, with no identified resistant strain since 2010 (MIC>2 µg/mL). Between 2001 (n=67) and 2012 (n=9), the number of NmC meningitis cases decreased by 87%. CONCLUSION: With more than 4800 bacterial meningitis cases reported in 12 years, this nationwide survey provides essential information on the microbiological and clinical characteristics of bacterial meningitis (epidemiology or resistance data). These results could lead to changing antibiotic treatment of pneumococcal meningitis before the results of antibiotic susceptibility tests.


Subject(s)
Meningitis, Bacterial/epidemiology , Meningitis, Bacterial/microbiology , Adolescent , Anti-Bacterial Agents/therapeutic use , Bacterial Vaccines/therapeutic use , Child , Child, Preschool , Drug Resistance, Bacterial , France/epidemiology , Humans , Infant , Infant, Newborn , Meningitis, Bacterial/drug therapy
5.
Clin Microbiol Infect ; 20(12): O1136-44, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24962059

ABSTRACT

Sorbitol-fermenting Escherichia coli O157:[H7] is a particularly virulent clone of E. coli O157:H7 associated with a higher incidence of haemolytic uraemic syndrome and a higher case fatality rate. Many fundamental aspects of its epidemiology remain to be elucidated, including its reservoir and transmission routes and vehicles. We describe an outbreak of sorbitol-fermenting E. coli O157:[H7] that occurred in France in 2011. Eighteen cases of paediatric haemolytic uraemic syndrome with symptom onset between 6 June and 15 July 2011 were identified among children aged 6 months to 10 years residing in northern France. A strain of sorbitol-fermenting E. coli O157:[H7] stx2a eae was isolated from ten cases. Epidemiological, microbiological and trace-back investigations identified multiply-contaminated frozen ground beef products bought in a supermarket chain as the outbreak vehicle. Strains with three distinct pulsotypes that were isolated from patients, ground beef preparations recovered from patients' freezers and from stored production samples taken at the production plant were indistinguishable upon molecular comparison. This investigation documents microbiologically confirmed foodborne transmission of sorbitol-fermenting of E. coli O157 via beef and could additionally provide evidence of a reservoir in cattle for this pathogen.


Subject(s)
Disease Outbreaks , Escherichia coli O157/isolation & purification , Foodborne Diseases/epidemiology , Hemolytic-Uremic Syndrome/epidemiology , Animals , Cattle , Escherichia coli O157/metabolism , Fermentation , Foodborne Diseases/microbiology , France/epidemiology , Hemolytic-Uremic Syndrome/microbiology , Humans , Meat/microbiology , Sorbitol/metabolism
6.
Eur J Clin Microbiol Infect Dis ; 32(8): 1041-7, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23471481

ABSTRACT

The purpose of this investigation was to describe the clinical and biological characteristics and evolution of invasive Fusobacterium infections in children admitted to two French paediatric tertiary care centres. Children who were admitted from 1998 to 2009 to two tertiary care centres for invasive Fusobacterium infection were included in a retrospective study. Thirty-one children with a median age of 5.7 years (interquartile range, IQR [2.3; 9.3]) were included. Nine children had an underlying condition, most commonly sickle cell disease (n = 3) or immunodeficiency (n = 3). Two children had skin effraction prior to the infection. The major sites of infection were the head and neck (n = 14) and abdomen (n = 10). Three children suffered from atypical Lemierre's syndrome. More than half of the children had a bacterial co-infection (58 %). Six children were hospitalised in an intensive care unit, and 67 % of them had a chronic underlying disease. None of the children died. Six children with negative cultures had Fusobacterium identified through 16S RNA-PCR. Fusobacterium is responsible for severe infection in children. Microbiological diagnosis might be improved by the wider use of molecular detection.


Subject(s)
Fusobacterium Infections/epidemiology , Fusobacterium/isolation & purification , Adolescent , Anti-Bacterial Agents/therapeutic use , Chi-Square Distribution , Child , Child, Preschool , Female , France/epidemiology , Fusobacterium Infections/drug therapy , Fusobacterium Infections/microbiology , Humans , Infant , Male , Retrospective Studies , Risk Factors , Statistics, Nonparametric , Tertiary Care Centers
7.
Eur J Clin Microbiol Infect Dis ; 32(6): 787-93, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23340863

ABSTRACT

We aimed to assess the independent effect of clinical spectrum, bacterial inoculum size and physician characteristics on the sensitivity of a rapid antigen detection test (RADT) for group A streptococcus (GAS) in children. Double throat swabs were collected from 1,482 children with pharyngitis and 294 asymptomatic children in a French prospective, office-based, multicenter (n = 17) study, from October 2009 to May 2011. Patient- and physician-level factors potentially affecting RADT sensitivity were studied by univariate and multivariate multilevel analysis, with laboratory throat culture as the reference test. In children with pharyngitis and asymptomatic children, the prevalence of GAS was 38 % (95 % confidence interval 36-41 %) and 11 % (7-14 %), respectively. Overall, RADT sensitivity was 87 % (84-90 %). On stratified and multivariate multilevel analysis, RADT sensitivity was higher for children with pharyngitis than asymptomatic children (89 % vs. 41 %), children <9 than ≥ 9 years old (88 % vs. 79 %) and those with heavy than light inoculum (94 % vs. 53 %). RADT sensitivity was influenced by the physician performing the test (range 56-96 %, p = 0.01) and was higher for physicians with hospital-based clinical activity in addition to office-based practice (adjusted odds ratio 3.4 [95 % confidence interval 1.9-6.3], p < 0.001); inter-physician variations in RADT sensitivity were largely explained by this variable (proportional change in variance >99 %). The sensitivity of the RADT is independently affected by patient- and physician-level factors. Physicians who base their diagnosis of GAS pharyngitis on the results of a RADT alone should consider diagnostic accuracy monitoring and adequate training when needed.


Subject(s)
Antigens, Bacterial , Pharyngitis/diagnosis , Pharyngitis/microbiology , Physicians , Streptococcal Infections/diagnosis , Streptococcal Infections/microbiology , Streptococcus pyogenes , Adolescent , Antigens, Bacterial/immunology , Child , Child, Preschool , Clinical Competence , Female , Humans , Immunologic Tests , Male , Middle Aged , Sensitivity and Specificity , Streptococcus pyogenes/immunology , Streptococcus pyogenes/isolation & purification , Surveys and Questionnaires
8.
Eur J Clin Microbiol Infect Dis ; 32(1): 107-13, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22907333

ABSTRACT

The outcome of bacterial bloodstream infections during pregnancy has greatly improved over the last few decades. However, there are no recent data on the characteristics of bacteremia in pregnant women. The aim of this study was to describe clinical and microbiological features of bacteremia and to assess maternal and fetal outcome. This retrospective study was conducted in the obstetrics departments of five teaching hospitals in Paris, France, from 2005 to 2009. The incidence of bacteremia was 0.3%. The most common sources of bacteremia were chorioamnionitis (47%) and the most common pathogen isolated was Escherichia coli. Empirical antimicrobial therapy was inappropriate in 29% of bacteremia cases, mostly (65%) when secondary to infection with an aminopenicillin-resistant microorganism. Bacteremia during pregnancy was associated with a 10% fetal mortality. Bacteremia during pregnancy is a rare occurrence, but it is associated with an unexpectedly poor fetal outcome and a high mortality rate.


Subject(s)
Bacteremia/epidemiology , Bacteremia/microbiology , Fetal Mortality , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/microbiology , Adult , Anti-Bacterial Agents/therapeutic use , Bacteremia/complications , Bacteremia/pathology , Bacteria/classification , Bacteria/isolation & purification , Female , Hospitals, Teaching , Humans , Incidence , Infant, Newborn , Middle Aged , Paris/epidemiology , Postpartum Period , Pregnancy , Pregnancy Complications, Infectious/drug therapy , Pregnancy Complications, Infectious/pathology , Retrospective Studies , Young Adult
9.
Arch Pediatr ; 19 Suppl 3: S109-16, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23178131

ABSTRACT

Urinary tract infections is one of the most common bacterial infections in pediatrics The increasing involvement of multiresistant bacteria including E. coli producing extended spectrum ß-lactamase (ESBL) makes its management difficult. The purpose of this article is to evaluate the state of the art and to propose ways of thinking about the management of E. coli urinary tract infection in children. The current percentage (less than 10%) of E. coli strains resistant to third generation cephalosporins and the relative efficiency of the latter, should not led to an immediate change of our protocols. Nevertheless, we should verify as soon as possible susceptibility of E. coli responsible for urinary tract infections and consider other therapeutic options for initial therapy and adaptation after obtaining antibiogram. The use of an aminoglycosid as initial treatment seems very interesting. Aminoglycosides have a very good distribution in the renal parenchyma and are still working on the majority of ESBL-producing bacteria. A rapid oral relay after 48 to 72 hours may be proposed according to the results of the susceptibility with either cotrimoxazole, cefixime, ciprofloxacin or an association cefixime-amoxicilline/clavulanate. The treatment of cystitis due to ESBL E. coli is much less problematic given the good urinary beta-lactam antibiotics diffusion. If clinical improvement occurs, even if antibiogram shows that the strain is resistant to the antibiotic prescribed, it is usually unnecessary to change treatment.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Escherichia coli Infections/drug therapy , Urinary Tract Infections/drug therapy , Algorithms , Child , Drug Resistance, Bacterial , Escherichia coli/drug effects , Escherichia coli/enzymology , Humans , Practice Guidelines as Topic , Pyelonephritis/drug therapy , Pyelonephritis/microbiology , beta-Lactamases/biosynthesis
10.
Arch Pediatr ; 19 Suppl 3: S129-34, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23178134

ABSTRACT

BACKGROUND: Neonatal bacterial meningitis has a mortality rate over 10 % and induces neurological sequellae in 20 to 50 % of cases. Escherichia coli (E. coli) is the second cause behind Group B streptococcus (GBS). The clinical and epidemiological features of neonatal meningitis due to E. coli between 2001 and 2010 with the data from the National Observatory are presented here. METHODS: Cases of child meningitis were prospectively collected since 2001 by a network of 252 pediatric wards associated with 166 microbiology laboratories. Risk factors, clinical signs, cerebrospinal fluid analysis, treatment and mortality were collected. RESULTS: 638 cases of neonatal bacterial meningitis were reported by 114 pediatric wards, among which 28 % (n=180) due to E. coli. If GBS prevailed in early and late-onset forms in term infants (84 % and 57 % for GBS vs 13 % and 28 % for E. coli), E. coli prevailed in preterm infants (42 % vs 37 % for GBS), and this trend increased in very preterm (GA < 33) (53 % vs 18 %). Number of E. coli early and late-onset meningitis didn't significantly vary over time. Antibiotherapy most often associated a 3(rd) generation cephalosporin, an aminosid and ciprofloxacin; sterilisation of the cerebrospinal fluid was achieved within day 2 to day 4 in 84 % of newborns. Only 3 strains were ESBL. Mortality was 11 % with E. coli, comparable to GBS (12 %) but reached 15 % in preterm infants. CONCLUSIONS: E. coli was the prevailing cause of early and late onset bacterial meningitis in premature infants, associated with a higher mortality than in term infants.


Subject(s)
Meningitis, Escherichia coli/epidemiology , Humans , Infant, Newborn , Prospective Studies
11.
Arch Pediatr ; 19 Suppl 3: S140-4, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23178136

ABSTRACT

Outcome of early and late onset E. coli neonatal meningitis is poor with 12% (term infant) to 18% (premature infant) mortality rates. Early complications are cerebral abscesses, ventriculitis and ischemo-haemorragic cerebral lesions. Long term sequelae, particularly neurosensorial [14-17%] and neurodevelopmental [10-17%] are frequent. Delayed or unadapted antibiotic treatment is associated with an excess of complications. Main risk factors are hemodynamic failure, apnea, seizures, hypoglycorachia and abnormal EEG. Antibiotics must be started as soon as possible with a third generation cephalosporin (3GC). Cefotaxime is the most largely 3GC used with good tolerance and the most appropriate Pk/PD parameters, frequently in association with ciprofloxacin. Experimentally, neuroprotective drugs were recently proposed to improve prognosis such as inflammatory inhibitors, leakage bacterial components inhibitors, PMN penetration inhibitors in CSF, apoptosis regulators. Clinically protective effect of corticosteroids is discussed. Ciprofloxacin has an intrinsic anti-inflammatory activity and seems interesting to use in addition to conventional antibiotherapy during the first days of treatment. Prevalence of 3GC-resistant E. coli is 5% in the vaginal flora of pregnant women in some hospitals in France; this rate leads to reconsider first line antibiotic treatment and to switch cephalosporin with meropenem in neonates with confirmed gram negative bacilli or 3GC-resistant E. coli meningitis.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Meningitis, Escherichia coli/drug therapy , Humans , Infant, Newborn , Practice Guidelines as Topic
12.
Arch Pediatr ; 19 Suppl 3: S77-9, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23178139

ABSTRACT

Escherichia coli is both a gastrointestinal tract commensal and a major pathogen. In recent years, E. coli is under fire from the news due to a better understanding of pathogenic factors, outbreaks of infections caused by enterohaemorrhagic strains, and last but not least, the worrying development of antibiotic resistance. Due to the absence of new compounds active against these strains, producing extended-spectrum ß-lactamases (ESBL) and frequently multiresistant to other antibiotics, their emergence will pose therapeutic problems for practitioners of all pediatric specialties. The gold standard treatment for severe infections due to ESBL-E. coli family is the penem class. The frequent use of penems promotes the emergence of strains resistant to carbapenems. Sparing carbapenems should be a clear objective for non life-threatening infections.


Subject(s)
Escherichia coli Infections , Anti-Bacterial Agents/therapeutic use , Child , Drug Resistance, Bacterial , Escherichia coli Infections/drug therapy , Humans
13.
Arch Pediatr ; 19 Suppl 3: S80-92, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23178140

ABSTRACT

Extraintestinal pathogenic Escherichia coli (ExPEC) causing urinary tract infections, bacteraemia or meningitis are characterized by a particular genetic background (phylogenetic group B2 and D) and the presence, within genetic pathogenicity islands (PAI) or plasmids, of genes encoding virulence factors involved in adhesion to epithelia, crossing of the body barriers (digestive, kidney, bloodbrain), iron uptake and resistance to the immune system. Among the many virulence factors described, two are particularly linked with a pathophysiological process: type P pili PapGII adhesin is linked with acute pyelonephritis, in the absence of abnormal flow of urine, and the K1 capsule is linked with neonatal meningitis. However, if the adhesin PapGII appears as the key factor of pyelonephritis, such that its absence in strain causing the infection is predictive of malformation or a vesico-ureteral reflux, the meningeal virulence of E. coli can not be reduced to a single virulence factor, but results from a combination of factors unique to each clone, and an imbalance between the immune defenses of the host and bacterial virulence.


Subject(s)
Escherichia coli/pathogenicity , Virulence Factors , Adhesins, Escherichia coli/physiology , Bacterial Toxins , Child , Escherichia coli Infections/microbiology , Escherichia coli Infections/physiopathology , Fimbriae, Bacterial/physiology , Humans , Infant, Newborn , Meningitis, Bacterial/microbiology , Meningitis, Bacterial/physiopathology , Urinary Tract Infections/microbiology , Urinary Tract Infections/physiopathology
14.
Arch Pediatr ; 19 Suppl 3: S93-6, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23178141

ABSTRACT

Extended-spectrum beta-lactamase (ESBLs) are defined as ß-lactamase able to hydrolyze all penicillins and cephalosporins with the exception of cephamycins (cefotixin, cefotetan), moxalactam and carbapenems and are encoded by mobile genes. The most frequently encountered ESBLs belong to the CTX-M, SHV, and TEM families. ESBLs were found first in Klebsiella pneumonia and then predominantly in E. coli. The incidence of patients with ESBLs E. coli increase since 2000 in Robert Debré Hospital in Paris. They were mainly implicated in urinary tract infections and less frequently in other infections such as materno-foetal infections or neonatal meningitis. An increase of consumption of carbapenems may lead to spread of carbapenem resistant organisms. Thus alternative to carbapenems for treatment of ESBL producers are needed.


Subject(s)
Enterobacteriaceae/enzymology , beta-Lactamases/biosynthesis , Anti-Bacterial Agents/therapeutic use , Child , Drug Resistance, Bacterial , Enterobacteriaceae/drug effects , Enterobacteriaceae Infections/drug therapy , Enterobacteriaceae Infections/microbiology , Humans
15.
Arch Pediatr ; 19 Suppl 3: S97-100, 2012 Nov.
Article in French | MEDLINE | ID: mdl-23178142

ABSTRACT

In 2011, an outbreak linked to a entero-haemorrhagic Escherichia coli strain, affecting adults more frequently, occurred in Germany, with 4320 bloody diarrhea cases, 850 cases of hemolytic uremic syndrome (HUS) and 82 deaths. Meanwhile, an epidemic affecting 24 patients took place in Bègle with similar epidemiological characteristics. These two strains were associated with consumption of contaminated seeds fenugreck by a particularly virulent strain belonging to a rare serotype, E. coli serotype O104:H4. This strain is a triple hybrid : it produces a shigatoxin, the adhesion at the gastrointestinal mucosa is related to the presence of fimbriae as enteroaggregants E. coli (ECAA), and has virulence factors of E. coli outer intestinal (EXPEC). In addition, it produced a ß-lactamasetype extended-spectrum CTXM15.


Subject(s)
Escherichia coli Infections/microbiology , Shiga-Toxigenic Escherichia coli/pathogenicity , Child , Disease Outbreaks , Escherichia coli Infections/epidemiology , Humans
16.
Arch Pediatr ; 19(10): 1132-9, 2012 Oct.
Article in French | MEDLINE | ID: mdl-22925540

ABSTRACT

BACKGROUND: Since 2001 in France, a nasopharyngeal carriage study was set up for children six to 24 months old. Any data are available for older children (25 to 60 months). The aim of this study is to compare the nasopharyngeal carriage in children with acute otitis media (AOM) or healthy between both age groups (6/24 months versus 25/60 months). Moreover, during the study period, the 13-valent pneumococcal conjugate vaccine (PCV13) has replaced PCV7 in June 2010. METHODS: From October 2010 to June 2011, 58 pediatricians obtained nasopharyngeal swabs from children 6-60 months with acute otitis media (AOM) or healthy controls, to analyse the carriage of pneumococcus, Haemophilus influenzae, Moraxella catarrhalis, group A streptococcus and Staphylococcus aureus. RESULTS: Of the 1557 enrolled children, 1258 were 6 to 24 months old (315 healthy and 943 AOM) and 299 were 25 to 60 months (102 healthy and 197 AOM). More then 85% were PCV7 vaccinated and the children of 25/60 months were rarely PCV13 vaccinated (14.1%) compared to younger children (69.9%, P<0.001). For children 6/24 months, the Streptococcus pneumoniae carriage was higher in AOM group (57.3%) versus healthy (28.9%). By contrast for older children, the difference (58.4% versus 50%) was not significant. In the healthy group, older children carried more often S. pneumoniae than younger children (50% versus 28.9%, P<0.0001). This trend was also observed for H. influenzae carriage (49% versus 18.7%, P<0.0001). Multivariate analysis in the healthy group showed that siblings and day care center (or school) increased the carriage of S. pneumoniae and H. influenzae. CONCLUSION: These data from nasopharyngeal carriage in children 6 to 60 months old showed that pneumococcus and H. influenzae carriage is high for patients under 2 years, especially in the healthy group. Moreover, these data from the transition PCV7/PCV13, will serve as baseline in France to evaluate the impact of PCV13.


Subject(s)
Carrier State/microbiology , Nasopharynx/microbiology , Pneumococcal Vaccines , Case-Control Studies , Child Day Care Centers , Child, Preschool , Female , France , Haemophilus influenzae/isolation & purification , Humans , Infant , Male , Multivariate Analysis , Otitis Media/microbiology , Siblings , Streptococcus pneumoniae
17.
Arch Pediatr ; 19 Suppl 2: S49-54, 2012 Sep.
Article in French | MEDLINE | ID: mdl-22883366

ABSTRACT

BACKGROUND: The GPIP/ACTIV (Groupe de Pathologie Infectieuse Pédiatrique and Association Clinique et Thérapeutique Infantile du Val de Marne) set up an active surveillance network to analyze the epidemiological, clinical and biological features of meningococcal meningitis. METHODS: French pediatric wards working with 166 microbiology laboratories enrolled all children (0-18 years old) with bacterial meningitis. Risk factors, signs and symptoms, vaccination status, cerebrospinal fluid analysis, treatments and case fatality rate were recorded. RESULTS: Since 2001, 1661 meningococcal meningitis were reported among 3769 (44.1%) bacterial meningitis. Mean age was 4.4- year- old (± 4.8, median 2.5) and 2/3 cases occurred in children under 5- year- old (68.8%). Serogroup B (61.3%) is preponderant following by serogroup C (27.0%). 27.5% of children had received an antibiotic treatment 24 hours before lumbar puncture. A shock is reported in 31.0% of cases. No cases of meningococcal meningitis C has been reported in children vaccinated with a conjugate vaccine. Two children vaccinated with MenBvac(®) vaccine had a meningitis B14:P1.7,16. Global case fatality rate was 6.5% but was higher (9.2%) for serogroup C than for serogroup B (5.9%) (p=0.02). CONCLUSION: This is among the largest series of microbiologically documented meningococcal meningitis to date (1661 cases). In France, meningococcal is responsible for approximately 50 % of meningitis. Effective meningococcal serogroup B vaccine and serogroup C vaccination recommendation could control the burden of meningococcal meningitis.


Subject(s)
Meningitis, Meningococcal/microbiology , Meningitis, Meningococcal/prevention & control , Meningococcal Vaccines/administration & dosage , Neisseria meningitidis/pathogenicity , Vaccination , Adolescent , Anti-Bacterial Agents/therapeutic use , Child , Child, Preschool , Female , France/epidemiology , Humans , Incidence , Infant , Infant, Newborn , Male , Meningitis, Meningococcal/cerebrospinal fluid , Meningitis, Meningococcal/diagnosis , Meningitis, Meningococcal/mortality , Meningitis, Meningococcal/therapy , Neisseria meningitidis/isolation & purification , Neisseria meningitidis, Serogroup B/pathogenicity , Neisseria meningitidis, Serogroup C/pathogenicity , Risk Factors , Serotyping , Societies, Medical , Spinal Puncture , Survival Rate , Treatment Outcome , Vaccination/methods , Vaccines, Conjugate/administration & dosage
18.
Eur J Clin Microbiol Infect Dis ; 31(10): 2773-81, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22569646

ABSTRACT

Streptococcus pneumoniae is an uncommon cause of osteoarticular infections (OAI) in children. The objective of this study was to investigate the clinical and laboratory characteristics of pneumococcal OAI before and after the introduction of the heptavalent pneumococcal conjugate vaccine (PCV7). Data were retrospectively collected from children aged <16 years who were hospitalized for pneumococcal OAI between 1997 and 2007 in four Parisian teaching hospitals. Forty-three children were included (32 with arthritis and 11 with osteomyelitis) and the median age of these children was 12.5 months (range 3 months to 14 years). Serotypes were available for 19/43 strains (44 %) from 1997 onwards and for 12/13 strains (92 %) from 2005 onwards. Seven unvaccinated children were infected with vaccine serotypes and we observed only one vaccine failure. After the introduction of PCV7, we noted an increase in short-term complications and the emergence of serotype 19A, which was penicillin-intermediate in 86 % of cases. After PCV7 introduction, serotype 19A was the most frequent serotype implicated in pediatric pneumococcal OAI. The 13-valent pneumococcal conjugate vaccine introduced in France in June 2010 should cover the emerging serotype.


Subject(s)
Arthritis, Infectious/microbiology , Osteomyelitis/microbiology , Pneumococcal Infections/epidemiology , Pneumococcal Vaccines/administration & dosage , Adolescent , Arthritis, Infectious/epidemiology , Child , Child, Preschool , Female , France/epidemiology , Heptavalent Pneumococcal Conjugate Vaccine , Hospitalization , Humans , Incidence , Infant , Male , Microbial Sensitivity Tests , Osteomyelitis/epidemiology , Penicillins/pharmacology , Retrospective Studies , Synovial Fluid/microbiology , Treatment Outcome , Vaccination/standards , Young Adult
19.
Eur J Clin Microbiol Infect Dis ; 31(10): 2827-34, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22639173

ABSTRACT

Nosocomial outbreaks of extended-spectrum ß-lactamase (ESBL)-producing Klebsiella pneumoniae are an increasing concern in neonatal intensive care units (NICUs). We describe an outbreak of ESBL-producing K. pneumoniae that lasted 5 months and affected 23 neonates in our NICU. Proton pump inhibitor and extended-spectrum cephalosporin exposure were significantly associated with the risk of ESBL-producing K. pneumoniae colonisation and/or infection. Thirty isolates recovered from clinical, screening and environmental samples in the NICU were studied by means of Raman spectroscopy, pulsed-field gel electrophoresis and repetitive extragenic palindromic polymerase chain reaction (rep-PCR). The Raman clustering was in good agreement with the results of the other two molecular methods. Fourteen isolates belonged to the Raman clone 1 and 16 to the Raman clone 3. Molecular analysis showed that all the strains expressed SHV-1 chromosomal resistance, plasmid-encoded TEM-1 and CTX-M-15 ß-lactamases. Incompatibility groups of plasmid content identified by PCR-based replicon typing indicated that resistance dissemination was due to the clonal spread of K. pneumoniae and horizontal CTX-M-15 gene transfer between the two clones.


Subject(s)
Disease Outbreaks , Disease Transmission, Infectious , Intensive Care Units, Neonatal , Klebsiella Infections/transmission , Klebsiella pneumoniae/pathogenicity , beta-Lactamases/metabolism , Amoxicillin-Potassium Clavulanate Combination/pharmacology , Bacterial Typing Techniques , Cefotaxime/pharmacology , Drug Resistance, Multiple, Bacterial , Electrophoresis, Gel, Pulsed-Field , Female , Fomites/microbiology , France/epidemiology , Genes, Bacterial , Gestational Age , Humans , Infant, Newborn , Klebsiella Infections/epidemiology , Klebsiella Infections/microbiology , Klebsiella pneumoniae/enzymology , Klebsiella pneumoniae/genetics , Male , Microbial Sensitivity Tests , Plasmids/genetics , Plasmids/metabolism , Polymerase Chain Reaction , Risk Factors , Spectrum Analysis, Raman , beta-Lactamases/genetics
20.
Eur J Clin Microbiol Infect Dis ; 31(10): 2817-26, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22610663

ABSTRACT

M/emm typing, based either on serotyping of the M protein or on sequencing of the emm gene, is a major tool for epidemiological studies of group A streptococci (GAS). In order to simplify M/emm typing, we designed two multiplex polymerase chain reaction (PCR) formats capable of identifying the most frequent GAS M/emm types involved in invasive infections and antimicrobial resistance. A heptaplex PCR procedure was first developed in a conventional format coupled with gel electrophoresis to identify emm types 1, 3, 4, 6, 12, 28, and 89, based on the size of the amplification products. The other method, designed to identify the same seven emm types, together with emm11, was based on a real-time PCR format coupled with high-resolution melting (HRM) analysis, allowing the rapid typing of large strain collections.


Subject(s)
Antigens, Bacterial/analysis , Bacterial Outer Membrane Proteins/analysis , Bacterial Typing Techniques/methods , Carrier Proteins/analysis , Drug Resistance, Bacterial , Multiplex Polymerase Chain Reaction/methods , Streptococcal Infections/microbiology , Streptococcus/isolation & purification , Adolescent , Anti-Infective Agents/pharmacology , Child , Child, Preschool , DNA, Bacterial/analysis , Electrophoresis, Agar Gel/methods , Erythromycin/pharmacology , Genes, Bacterial , Humans , Infant , Infant, Newborn , Nucleic Acid Denaturation , Reproducibility of Results , Sensitivity and Specificity , Streptococcal Infections/blood , Streptococcal Infections/epidemiology , Streptococcus/classification , Streptococcus/drug effects , Streptococcus/genetics , Time Factors
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