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1.
Front Microbiol ; 14: 1194243, 2023.
Article in English | MEDLINE | ID: mdl-37485516

ABSTRACT

In June 2021, a cluster of seven cases of Campylobacter fetus infections occurred in a rehabilitation center and caused significant morbidity in elderly patients including five with bacteremia and two with osteoarticular medical device infections. The genetic identity identified by whole genome sequencing of the different Campylobacter fetus strains confirms a common source. This foodborne illness outbreak may have resulted from the consumption of unpasteurized dairy products, such as a cow's raw milk cheese resulting from a farm-to-fork strategy.

2.
Microbiol Spectr ; 9(2): e0113821, 2021 10 31.
Article in English | MEDLINE | ID: mdl-34668768

ABSTRACT

The aim of this study was to evaluate diagnostic means, host factors, delay of occurrence, and outcome of patients with COVID-19 pneumonia and fungal coinfections in the intensive care unit (ICU). From 1 February to 31 May 2020, we anonymously recorded COVID-19-associated pulmonary aspergillosis (CAPA), fungemia (CA-fungemia), and pneumocystosis (CA-PCP) from 36 centers, including results on fungal biomarkers in respiratory specimens and serum. We collected data from 154 episodes of CAPA, 81 of CA-fungemia, 17 of CA-PCP, and 5 of other mold infections from 244 patients (male/female [M/F] ratio = 3.5; mean age, 64.7 ± 10.8 years). CA-PCP occurred first after ICU admission (median, 1 day; interquartile range [IQR], 0 to 3 days), followed by CAPA (9 days; IQR, 5 to 13 days), and then CA-fungemia (16 days; IQR, 12 to 23 days) (P < 10-4). For CAPA, the presence of several mycological criteria was associated with death (P < 10-4). Serum galactomannan was rarely positive (<20%). The mortality rates were 76.7% (23/30) in patients with host factors for invasive fungal disease, 45.2% (14/31) in those with a preexisting pulmonary condition, and 36.6% (34/93) in the remaining patients (P = 0.001). Antimold treatment did not alter prognosis (P = 0.370). Candida albicans was responsible for 59.3% of CA-fungemias, with a global mortality of 45.7%. For CA-PCP, 58.8% of the episodes occurred in patients with known host factors of PCP, and the mortality rate was 29.5%. CAPA may be in part hospital acquired and could benefit from antifungal prescription at the first positive biomarker result. CA-fungemia appeared linked to ICU stay without COVID-19 specificity, while CA-PCP may not really be a concern in the ICU. Improved diagnostic strategy for fungal markers in ICU patients with COVID-19 should support these hypotheses. IMPORTANCE To diagnose fungal coinfections in patients with COVID-19 in the intensive care unit, it is necessary to implement the correct treatment and to prevent them if possible. For COVID-19-associated pulmonary aspergillosis (CAPA), respiratory specimens remain the best approach since serum biomarkers are rarely positive. Timing of occurrence suggests that CAPA could be hospital acquired. The associated mortality varies from 36.6% to 76.7% when no host factors or host factors of invasive fungal diseases are present, respectively. Fungemias occurred after 2 weeks in ICUs and are associated with a mortality rate of 45.7%. Candida albicans is the first yeast species recovered, with no specificity linked to COVID-19. Pneumocystosis was mainly found in patients with known immunodepression. The diagnosis occurred at the entry in ICUs and not afterwards, suggesting that if Pneumocystis jirovecii plays a role, it is upstream of the hospitalization in the ICU.


Subject(s)
COVID-19/epidemiology , Coinfection/mortality , Fungemia/epidemiology , Pneumonia, Pneumocystis/epidemiology , Pulmonary Aspergillosis/epidemiology , Aged , Antifungal Agents/therapeutic use , COVID-19/mortality , COVID-19/pathology , Coinfection/epidemiology , Critical Care , Female , France/epidemiology , Fungemia/drug therapy , Fungemia/mortality , Galactose/analogs & derivatives , Galactose/blood , Humans , Intensive Care Units/statistics & numerical data , Male , Mannans/blood , Middle Aged , Pneumonia, Pneumocystis/drug therapy , Pneumonia, Pneumocystis/mortality , Pulmonary Aspergillosis/drug therapy , Pulmonary Aspergillosis/mortality , Retrospective Studies , SARS-CoV-2 , Treatment Outcome
3.
Emerg Infect Dis ; 21(12): 2122-6, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26584467

ABSTRACT

We report 2 cases of pulmonary Bordetella hinzii infection in immunodeficient patients. One of these rare cases demonstrated the potential transmission of the bacteria from an avian reservoir through occupational exposure and its persistence in humans. We establish bacteriologic management of these infections and suggest therapeutic options if needed.


Subject(s)
Bordetella Infections/microbiology , Respiratory Tract Infections/microbiology , Adult , Aged , Animals , Bordetella Infections/epidemiology , Bordetella Infections/transmission , Humans , Immunocompromised Host , Lung Diseases/microbiology , Male , Opportunistic Infections/microbiology , Opportunistic Infections/transmission , Poultry/microbiology , Respiratory Tract Infections/epidemiology
4.
J Clin Microbiol ; 53(8): 2703-5, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25994161

ABSTRACT

From 2008 to 2013, 39 Helcococcus kunzii strains were collected from human clinical specimens (79% from foot ulcers), and 85% of the 39 patients were infected. Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry and molecular methods accurately identified all isolates. This large study of clinical observations confirms the potential pathogenic role of H. kunzii.


Subject(s)
Bacteriological Techniques/methods , Firmicutes/classification , Firmicutes/isolation & purification , Gram-Positive Bacterial Infections/epidemiology , Gram-Positive Bacterial Infections/microbiology , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Adult , Aged , Aged, 80 and over , Anti-Bacterial Agents/therapeutic use , Female , Firmicutes/chemistry , Gram-Positive Bacterial Infections/pathology , Humans , Male , Middle Aged , Young Adult
5.
J Clin Microbiol ; 53(4): 1423-7, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25609723

ABSTRACT

We report a case of foot infection by Clostridium sordellii and review 15 human infections registered at a Reference Center in France during the period 1998 to 2011. All strains were found nontoxigenic, lacking the lethal toxin gene coding for TcsL. Like Clostridium septicum, several C. sordellii infections were associated with intestinal neoplasms.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Clostridium Infections/microbiology , Clostridium sordellii/isolation & purification , Foot Diseases/microbiology , Adult , Aged , Aged, 80 and over , Clostridium Infections/drug therapy , Clostridium Infections/epidemiology , Female , France/epidemiology , Humans , Male , Middle Aged , Molecular Sequence Data
6.
Diagn Microbiol Infect Dis ; 74(3): 299-302, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22901791

ABSTRACT

Misidentification of rare Clostridium species often originated from the environment as clinically relevant species is problematic. A strain isolated from a traumatic leg wound first identified as C. clostridioforme was finally identified as the rare Clostridium celerecrescens. Two similar misidentifications are reported in the literature. In order to help the phenotypic differentiation of C. celerecrescens from the close species of the "C. clostridioforme group", an identification table and differential susceptibilities to 4 selected antibiotics are proposed. Once a clinical isolate is referred to this group, identification should be definitively confirmed by unambiguous methods such as 16s rDNA sequencing.


Subject(s)
Clostridium Infections/diagnosis , Clostridium Infections/microbiology , Clostridium/isolation & purification , Clostridium/pathogenicity , Wound Infection/microbiology , Wound Infection/pathology , Anti-Bacterial Agents/pharmacology , Bacterial Typing Techniques , Clostridium/classification , Clostridium/genetics , Clostridium Infections/pathology , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Humans , Male , Microbial Sensitivity Tests , Molecular Sequence Data , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Wounds and Injuries/complications , Young Adult
7.
Emerg Infect Dis ; 17(4): 612-8, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21470449

ABSTRACT

We report the repeated isolation of Bordetella petrii in the sputum of a 79-year-old female patient with diffuse bronchiectasis and persistence of the bacterium for >1 year. The patient was first hospitalized due to dyspnea, which developed into severe cough with purulent sputum that yielded B. petrii on culture. After this first episode, the patient was hospitalized an additional 4 times with bronchorrhea symptoms. The isolates collected were analyzed by using biochemical, genotypic, and proteomic tools. Expression of specific proteins was analyzed by using serum samples from the patient. The B. petrii isolates were compared with other B. petrii isolates collected from humans or the environment and with isolates of B. pertussis, B. parapertussis, B. bronchiseptica, and B. holmesii, obtained from human respiratory tract infections. Our observations indicate that B. petrii can persist in persons with chronic pulmonary obstructive disease as has been previously demonstrated for B. bronchiseptica.


Subject(s)
Bordetella Infections/microbiology , Bordetella/physiology , Aged , Anti-Bacterial Agents/pharmacology , Bacterial Proteins/metabolism , Bordetella/drug effects , Bordetella/genetics , Bordetella/isolation & purification , Chromosomes, Bacterial/genetics , Female , Genome, Bacterial/genetics , Humans , Molecular Sequence Data , RNA, Ribosomal, 16S/genetics , Sequence Analysis , Time Factors
8.
Am J Trop Med Hyg ; 84(4): 535-8, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21460005

ABSTRACT

We report a case of imported Plasmodium knowlesi malaria in a French tourist following a vacation in Thailand. This case shows, first, tourists may contract knowlesi malaria even only staying on the beach and second, the diagnosis remains difficult, even with polymerase chain reaction methods.


Subject(s)
Malaria/epidemiology , Malaria/parasitology , Plasmodium knowlesi/isolation & purification , Animals , Antimalarials/therapeutic use , France , Humans , Macaca , Male , Middle Aged , Thailand/epidemiology , Travel
9.
J Clin Microbiol ; 47(5): 1510-6, 2009 May.
Article in English | MEDLINE | ID: mdl-19297595

ABSTRACT

Burkholderia gladioli, primarily known as a plant pathogen, is involved in human infections, especially in patients with cystic fibrosis (CF). In the present study, the first respiratory isolates recovered from 14 French patients with CF and 4 French patients without CF, identified by 16S rRNA gene analysis, were tested for growth on B. cepacia selective media, for identification by commercial systems, and for their antimicrobial susceptibilities, and were compared by pulsed-field gel electrophoresis (PFGE). Patients' data were collected. All 18 isolates grew on oxidation-fermentation-polymyxin B-bacitracin-lactose medium and Pseudomonas cepacia agar, but only 13 grew on Burkholderia cepacia selective agar. API 20NE strips did not differentiate B. gladioli from B. cepacia, whereas Vitek 2 GN cards correctly identified 15 isolates. All isolates were susceptible to piperacillin, imipenem, aminoglycosides, and ciprofloxacin and were far less resistant to ticarcillin than B. cepacia complex organisms. Fifteen PFGE types were observed among the 18 isolates, but shared types were not identified among epidemiologically related patients. The microbiological follow-up of CF patients showed that colonization was persistent in 3 of 13 documented cases; B. gladioli was isolated from posttransplantation cultures of blood from 1 patient. Among the patients without CF, B. gladioli was associated with intubation (three cases) or bronchiectasis (one case). In summary, the inclusion of B. gladioli in the databases of commercial identification systems should improve the diagnostic capabilities of those systems. In CF patients, this organism is more frequently involved in transient infections than in chronic infections, but it may be responsible for complications posttransplantation; patient-to-patient transmission has not been demonstrated to date. Lastly, B. gladioli appears to be naturally susceptible to aminoglycosides and ciprofloxacin, although resistant isolates may emerge in the course of chronic infections.


Subject(s)
Burkholderia Infections/microbiology , Burkholderia gladioli/classification , Burkholderia gladioli/isolation & purification , Adolescent , Adult , Anti-Bacterial Agents/pharmacology , Bacterial Typing Techniques , Burkholderia gladioli/drug effects , Burkholderia gladioli/metabolism , Child , Child, Preschool , Cluster Analysis , Cystic Fibrosis/complications , DNA Fingerprinting , DNA, Bacterial/genetics , DNA, Ribosomal/genetics , Electrophoresis, Gel, Pulsed-Field , Female , France , Genotype , Humans , Male , Microbial Sensitivity Tests , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Young Adult
10.
Antimicrob Agents Chemother ; 51(12): 4342-50, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17709473

ABSTRACT

The excision of the staphylococcal chromosomal cassette mec (SCCmec) from methicillin-resistant Staphylococcus aureus (MRSA) strains results in methicillin-susceptible S. aureus (MSSA) strains. In order to determine the proportion and diversity of multidrug-resistant MSSA (MR-MSSA) strains derived from MRSA strains, 247 mecA-negative isolates recovered in 60 French hospitals between 2002 and 2004 were characterized. The spa types of all strains were determined, and a subset of the strains (n = 30) was further genotyped by multilocus sequence typing. The IDI-MRSA assay was used to test the isolates for the presence of the SCCmec element, which was detected in 68% of all isolates analyzed. Molecular analysis of the samples suggested that 92% of the MR-MSSA isolates were derived from MRSA clones of diverse genetic backgrounds, of which the clone of sequence type 8 and SCCmec type IV(A) accounted for most of the samples. High variations in incidence data and differences in the molecular characteristics of the isolates from one hospital to another indicate that the emergence of MR-MSSA resulted from independent SCCmec excisions from epidemic MRSA isolates, as well as the diffusion of methicillin-susceptible strains after the loss of SCCmec. MR-MSSA could constitute a useful model for the study of the respective genetic and environmental factors involved in the dissemination of S. aureus in hospitals.


Subject(s)
Methicillin/pharmacology , Staphylococcal Infections/drug therapy , Staphylococcus aureus/drug effects , Staphylococcus aureus/genetics , Bacterial Proteins/genetics , Bacterial Typing Techniques , Cross Infection/epidemiology , Cross Infection/microbiology , Drug Resistance, Multiple, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , France/epidemiology , Genes, Bacterial/genetics , Geography , Humans , Microbial Sensitivity Tests , Models, Genetic , Molecular Epidemiology , Penicillin-Binding Proteins , Polymerase Chain Reaction , Staphylococcal Infections/epidemiology , Staphylococcal Infections/microbiology , Staphylococcus aureus/classification
11.
J Clin Microbiol ; 43(8): 4191-3, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16081974

ABSTRACT

We report a detailed characterization of methicillin-susceptible Staphylococcus aureus isolates from five French hospitals negative for both the mecA and the ccrAB loci but positive for the IS431::pUB110::IS431::dcs structure, present in some Staphylococcus cassette chromosome mec (SCCmec) types. The presence of SCCmec-associated elements suggests that this unusual resistant phenotype is due to a partial excision of SCCmec from epidemic methicillin-resistant S. aureus. The hypothesis of a genetic relatedness is strengthened by common sequence and spa types and similar susceptibility patterns.


Subject(s)
Chromosomes, Bacterial , Methicillin Resistance/genetics , Staphylococcus aureus/drug effects , Staphylococcus aureus/genetics , Humans , Polymerase Chain Reaction
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