Nadia Andreani

Dr. Nadia Andreani

Department of Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, Plön, Germany
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 April 2017 in The ISME Journal
Verified
Journal Article
Open access
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NANadia Andreani
Nadia Andreani
EHElze Hesse
Elze Hesse
MVMichiel Vos
Michiel Vos
Many prokaryote species are known to have fluid genomes, with different strains varying markedly in accessory gene content through the combined action of gene loss, gene gain via lateral transfer, as well as gene duplication. However, the evolutionary forces determining genome fluidity are not yet well understood. We here for the first time systematically analyse the degree to which this distinctive genomic feature differs between bacterial species. We find that genome fluidity is positively correlated with synonymous nucleotide diversity of the core genome, a measure of effective population size Ne. No effects of genome size, phylogeny or homologous recombination rate on genome fluidity were found. Our findings are consistent with a scenario where accessory gene content turnover is for a large part dictated by neutral evolution.

1 May 2014 in Food Microbiology
Verified
Journal Article
Closed access
NANadia Andreani
Nadia Andreani
MMMaria Elena Martino
Maria Elena Martino
Luca FasolatoLuca Fasolato
Luca Fasolato
LCL. Carraro
L. Carraro
FMF. Montemurro
F. Montemurro
BCB. Cardazzo
B. Cardazzo

1 November 2015 in International Journal of Food Microbiology
Verified
Journal Article
Closed access
NANadia Andreani
Nadia Andreani
LCLisa Carraro
Lisa Carraro
MMMaria Elena Martino
Maria Elena Martino
Marco FondiMarco Fondi
Marco Fondi
LFLuca Fasolato
Luca Fasolato
BCBarbara Cardazzo
Barbara Cardazzo

31 January 2024 in Gut Microbes
Verified
Journal Article
Open access
NANadia Andreani
Nadia Andreani
ASArunabh Sharma
Arunabh Sharma
BDBrigitte Dahmen
Brigitte Dahmen
HSHannah E. Specht
Hannah E. Specht
NMNina Mannig
Nina Mannig
JSJochen Seitz
Jochen Seitz
There is mounting evidence regarding the role of gut microbiota in anorexia nervosa (AN). Previous studies have reported that patients with AN show dysbiosis compared to healthy controls (HCs); however, the underlying mechanisms are unclear, and data on influencing factors and longitudinal course of microbiome changes are scarce. Here, we present longitudinal data of 57 adolescent inpatients diagnosed with AN at up to nine time points (including a 1-year follow-up examination) and compare these to up to six time points in 34 HCs. 16S rRNA gene sequencing was used to investigate the microbiome composition of fecal samples, and data on food intake, weight change, hormonal recovery (leptin levels), and clinical outcomes were recorded. Differences in microbiome composition compared to HCs were greatest during acute starvation and in the low-weight group, while diminishing with weight gain and especially weight recovery at the 1-year follow-up. Illness duration and prior weight loss were strongly associated with microbiome composition at hospital admission, whereas microbial changes during treatment were associated with kilocalories consumed, weight gain, and hormonal recovery. The microbiome at admission was prognostic for hospital readmission, and a higher abundance of Sutterella was associated with a higher body weight at the 1-year follow-up. Identifying these clinically important factors further underlines the potential relevance of gut microbial changes and may help elucidate the underlying pathophysiology of gut-brain interactions in AN. The characterization of prognostically relevant taxa could be useful to stratify patients at admission and to potentially identify candidate taxa for future supplementation studies aimed at improving AN treatment.

1 August 2016 in Food Microbiology
Verified
Journal Article
Closed access
ESE. Sattin
E. Sattin
NANadia Andreani
Nadia Andreani
LCL. Carraro
L. Carraro
LFL. Fasolato
L. Fasolato
SBS. Balzan
S. Balzan
BCBarbara Cardazzo
Barbara Cardazzo

17 August 2016 in Frontiers in Microbiology
Verified
Journal Article
Open access
PDF file
ESEleonora Sattin
Eleonora Sattin
NANadia Andreani
Nadia Andreani
LCLisa Carraro
Lisa Carraro
RLRosaria Lucchini
Rosaria Lucchini
LFLuca Fasolato
Luca Fasolato
BCBarbara Cardazzo
Barbara Cardazzo
In the past, milk whey was only a by-product of cheese production, but currently, it has a high commercial value for use in the food industries. However, the regulation of whey management (i.e., storage and hygienic properties) has not been updated, and as a consequence, its microbiological quality is very challenging for food safety. The Next Generation Sequencing (NGS) technique was applied to several whey samples used for Ricotta production to evaluate the microbial community composition in depth using both RNA and DNA as templates for NGS library construction. Whey samples demonstrating a high microbial and aerobic spore load contained mostly Firmicutes; although variable, some samples contained a relevant amount of Gammaproteobacteria. Several lots of whey acquired as raw material for Ricotta production presented defective organoleptic properties. To define the volatile compounds in normal and defective whey samples, a headspace gas chromatography/mass spectrometry (GC/MS) analysis was conducted. The statistical analysis demonstrated that different microbial communities resulted from DNA or cDNA library sequencing, and distinguishable microbiota composed the communities contained in the organoleptic-defective whey samples.