Sara Romano-Bertrand

ORCID: 0000-0002-6134-2210
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About
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Research Areas
  • Hepatitis B Virus Studies
  • Vibrio bacteria research studies
  • Hepatitis C virus research
  • Antibiotic Resistance in Bacteria
  • Bacterial Identification and Susceptibility Testing
  • Nosocomial Infections in ICU
  • Infections and bacterial resistance
  • Liver Disease Diagnosis and Treatment
  • Data-Driven Disease Surveillance
  • Bacterial biofilms and quorum sensing
  • Health, Medicine and Society
  • Infection Control and Ventilation
  • Healthcare Systems and Practices
  • Genetic and Kidney Cyst Diseases
  • Antibiotic Use and Resistance
  • Genetic Syndromes and Imprinting
  • Cardiac Imaging and Diagnostics
  • Plant Pathogenic Bacteria Studies
  • Antimicrobial Resistance in Staphylococcus
  • Misinformation and Its Impacts
  • Infective Endocarditis Diagnosis and Management
  • Global Healthcare and Medical Tourism
  • Medical Device Sterilization and Disinfection
  • COVID-19 and healthcare impacts
  • Mycobacterium research and diagnosis

Université de Montpellier
2015-2025

Institut de Recherche pour le Développement
2018-2025

Laboratoire HydroSciences Montpellier
2016-2025

Centre National de la Recherche Scientifique
2018-2025

Centre Hospitalier Universitaire de Montpellier
2016-2025

Institut Français du Textile et de l'Habillement
2020-2021

Maladies Infectieuses et Vecteurs: Écologie, Génétique, Évolution et Contrôle
2018

Agropolis International
2018

Département Santé des Plantes et Environnement
2015-2017

Hôpital Saint Eloi
2015-2017

The human skin microbiota is quantitatively dominated by Gram-positive bacteria, detected both culture and metagenomics. However, metagenomics revealed a huge variety of Gram-negative taxa generally considered from environmental origin. For species affiliation bacteria in microbiota, clones 16S rRNA gene colonies growing on diverse media were analyzed. Species-level identification was achieved for 81% colonies. Fifty distributed 26 genera identified culture, mostly belonging to...

10.1016/j.onehlt.2016.02.002 article EN cc-by-nc-nd One Health 2016-03-05

Alström Syndrome (ALMS) is a rare genetic disorder (483 living cases), characterized by many clinical manifestations, including blindness, obesity, type 2 diabetes and cardiomyopathy. ALMS caused mutations in the ALMS1 gene, encoding for large protein with implicated roles ciliary function, cellular quiescence intracellular transport. Patients have extensive fibrosis nearly all tissues resulting progressive organ failure which often ultimate cause of death. To focus on role generation...

10.1371/journal.pone.0019081 article EN cc-by PLoS ONE 2011-04-26

Patients with a penicillin allergy label have an increased risk of surgical site infection. Although decision tree was published in 2019 to define which patients could benefit from direct cephalosporin use the perioperative setting, this strategy remains unvalidated. This consensus statement aimed adapt it based on expert cover persisting caveats and environment poor allergist resources. Perioperative antibiotic prophylaxis experts were invited participate. The Delphi method implemented...

10.1093/jacamr/dlaf024 article EN cc-by-nc JAC-Antimicrobial Resistance 2025-03-04

Abstract Background Ochrobactrum anthropi is a versatile bacterial species with strains living in very diverse habitats. It increasingly recognized as opportunistic pathogen hospitalized patients. The population biology of the particularly regard to characteristics human isolates being investigated. To address this issue, we proposed polyphasic approach consisting Multi-Locus Sequence Typing (MLST), multi-locus phylogeny, genomic-based fingerprinting by pulsed-field gel electrophoresis...

10.1186/1471-2180-9-267 article EN cc-by BMC Microbiology 2009-12-01

Ochrobactrum intermedium is considered as an emerging human environmental opportunistic pathogen with mild virulence. The distribution of isolates and sequences described in literature databases showed frequent association beings polluted environments. As population structures are related to bacterial lifestyles, we investigated by multi-locus approach the genetic structure a 65 representative known natural O. intermedium. was further surveyed for genome dynamics using pulsed-field gel...

10.1371/journal.pone.0083376 article EN cc-by PLoS ONE 2014-01-17

The naturally acquired microbiota of Anopheles can influence vector's susceptibility to Plasmodium and its capacity transmit them. Microbiota modification is a new challenge limit disease transmission but it still needs advanced knowledges on bacterial community in Anopheles, especially wild infected specimens from diverse origin species. Bacterial culture 16S rRNA gene-PCR associated Temporal Temperature Gradient Electrophoresis (TTGE) were applied explore the diversity abdomen 100 (eight...

10.3389/fmicb.2016.02095 article EN cc-by Frontiers in Microbiology 2016-12-23

Bettini V, Maffei P, Pagano C, Romano S, Milan G, Favaretto F, Marshall JD, Paisey R, Scolari Greggio NA, Tosetto I, Naggert JK, Sicolo N, Vettor R. The progression from obesity to type 2 diabetes in Alström syndrome. Background: syndrome (ALMS) is a rare autosomal recessive monogenic disease associated with obesity, hyperinsulinemia, and alterations of glucose metabolism that often lead the development at young age. Objective: To study relationship between weight group ALMS patients matched...

10.1111/j.1399-5448.2011.00789.x article EN Pediatric Diabetes 2011-07-03

Abstract While the selection of complex HBV drug‐resistance patterns on therapeutic failure can compromise efficacy anti‐HBV therapies, recent data show that patients failing treatment without have a rate virological success close to drug‐naive patients. The goal this study is defining, in clinical practice, burden mutations cohort treated with drugs. Prevalence and were analyzed by RT‐sequencing 204 infected chronically: 148 experiencing rebound (defined as an increase serum HBV‐DNA > 20...

10.1002/jmv.23567 article EN Journal of Medical Virology 2013-04-12

Alström syndrome (ALMS) is a rare autosomal recessive monogenic disease included in an emerging class of genetic disorders called 'ciliopathies' and likely to impact the central nervous system as well metabolic endocrine function. Individuals with ALMS present clinical features resembling growth hormone deficiency (GHD) condition, but thus far no study has specifically investigated this aspect large population.Twenty-three patients (age, 1-52 years; 11 males, 12 females) were evaluated for...

10.1111/cen.12180 article EN Clinical Endocrinology 2013-02-27

Alström syndrome (ALMS) is an autosomal recessive genetic disease with characteristic phenotypical features including multi-organ fibrosis, insulin resistance, obesity and type 2 diabetes. ALMS1, a ubiquitously expressed gene mutated in ALMS patients, gives rise to protein of unknown function localized basal bodies ciliated cells centrosomes. Together Bardet-Biedl syndrome, member ciliopathies, but the link between cilia/centrosome deficits metabolic abnormalities remains be determined. In...

10.3892/ijmm.21.6.731 article EN International Journal of Molecular Medicine 2008-06-01

In the context of a methicillin-susceptible Staphylococcus aureus (MSSA) outbreak, we aimed to improve our knowledge S. (SA) epidemiology in neonatal care center (NCC) tertiary teaching hospital.We performed complete one-year review SA carrier, colonized or infected patients. Monthly prevalence and incidence intestinal carriage, colonization infection were calculated types analysed. During MSSA strains studied for antimicrobial resistance, content virulence genes comparative fingerprint...

10.1186/2047-2994-3-21 article EN cc-by Antimicrobial Resistance and Infection Control 2014-07-01
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