Jan Knol

Prof. Jan Knol


Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

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

Representative Publications

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Verified
Journal Article
Open access
PDF file
CWCarrie Wegh
Carrie Wegh
SGSharon Geerlings
Sharon Geerlings
JKJan Knol
Jan Knol
RGROESELERS Guus
ROESELERS Guus
CBClara Belzer
Clara Belzer
Postbiotics are functional bioactive compounds, generated in a matrix during fermentation, which may be used to promote health. The term postbiotics can be regarded as an umbrella term for all synonyms and related terms of these microbial fermentation components. Therefore, postbiotics can include many different constituents including metabolites, short-chain fatty acids (SCFAs), microbial cell fractions, functional proteins, extracellular polysaccharides (EPS), cell lysates, teichoic acid, peptidoglycan-derived muropeptides and pili-type structures. Postbiotics is also a rather new term in the ‘-biotics’ field. Where consensus exists for the definitions of pre- and probiotics, this is not yet the case for postbiotics. Here we propose a working definition and review currently known postbiotic compounds, their proposed mechanisms, clinical evidence and potential applications. Research to date indicates that postbiotics can have direct immunomodulatory and clinically relevant effects and evidence can be found for the use of postbiotics in healthy individuals to improve overall health and to relief symptoms in a range of diseases such as infant colic and in adults atopic dermatitis and different causes of diarrhea.

8 November 2017 in mBio
Verified
Journal Article
Open access
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CBClara Belzer
Clara Belzer
LCLoo Wee Chia
Loo Wee Chia
SASteven Aalvink
Steven Aalvink
BCBhawani Chamlagain
Bhawani Chamlagain
VPVieno Piironen
Vieno Piironen
WVWillem M. de Vos
Willem M. de Vos
Akkermansia muciniphilahas evolved to specialize in the degradation and utilization of host mucus, which it may use as the sole source of carbon and nitrogen. Mucus degradation and fermentation byA. muciniphilaare known to result in the liberation of oligosaccharides and subsequent production of acetate, which becomes directly available to microorganisms in the vicinity of the intestinal mucosa. Coculturing experiments ofA.muciniphilawith non-mucus-degrading butyrate-producing bacteriaAnaerostipes caccae,Eubacterium hallii, andFaecalibacterium prausnitziiresulted in syntrophic growth and production of butyrate. In addition, we demonstrate that the production of pseudovitamin B12byE. halliiresults in production of propionate byA. muciniphila, which suggests that this syntrophy is indeed bidirectional. These data are proof of concept for syntrophic and other symbiotic microbe-microbe interactions at the intestinal mucosal interface. The observed metabolic interactions betweenA.muciniphilaand butyrogenic bacterial taxa support the existence of colonic vitamin and butyrate production pathways that are dependent on host glycan production and independent of dietary carbohydrates. We infer that the intestinal symbiontA. muciniphilacan indirectly stimulate intestinal butyrate levels in the vicinity of the intestinal epithelial cells with potential health benefits to the host.IMPORTANCEThe intestinal microbiota is said to be a stable ecosystem where many networks between microorganisms are formed. Here we present a proof of principle study of microbial interaction at the intestinal mucus layer. We show that indigestible oligosaccharide chains within mucus become available for a broad range of intestinal microbes after degradation and liberation of sugars by the speciesAkkermansia muciniphila. This leads to the microbial synthesis of vitamin B12, 1,2-propanediol, propionate, and butyrate, which are beneficial to the microbial ecosystem and host epithelial cells.

1 March 2014 in Brain, Behavior, and Immunity
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Journal Article
Closed access
CTCaroline G.M. de Theije
Caroline G.M. de Theije
HWHarm Wopereis
Harm Wopereis
MRMohamed Ramadan
Mohamed Ramadan
TETiemen van Eijndthoven
Tiemen van Eijndthoven
JLJolanda Lambert
Jolanda Lambert
RORaish Oozeer
Raish Oozeer

30 June 2016 in PLOS ONE
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Journal Article
Open access
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RMRocio Martin
Rocio Martin
HMHiroshi Makino
Hiroshi Makino
AYAysun Cetinyurek Yavuz
Aysun Cetinyurek Yavuz
KBKaouther Ben-Amor
Kaouther Ben-Amor
MRMieke Roelofs
Mieke Roelofs
JKJan Knol
Jan Knol
Colonization of the infant gut is believed to be critically important for a healthy growth as it influences gut maturation, metabolic, immune and brain development in early life. Understanding factors that influence this process is important, since an altered colonization has been associated with a higher risk of diseases later in life. Fecal samples were collected from 108 healthy neonates in the first half year of life. The composition and functionality of the microbiota was characterized by measuring 33 different bacterial taxa by qPCR/RT qPCR, and 8 bacterial metabolites. Information regarding gender, place and mode of birth, presence of siblings or pets; feeding pattern and antibiotic use was collected by using questionnaires. Regression analysis techniques were used to study associations between microbiota parameters and confounding factors over time. Bacterial DNA was detected in most meconium samples, suggesting bacterial exposure occurs in utero. After birth, colonization by species of Bifidobacterium, Lactobacillus and Bacteroides was influenced by mode of delivery, type of feeding and presence of siblings, with differences found at species level and over time. Interestingly, infant-type bifidobacterial species such as B. breve or B. longum subsp infantis were confirmed as early colonizers apparently independent of the factors studied here, while B. animalis subsp. lactis presence was found to be dependent solely on the type of feeding, indicating that it might not be a common infant gut inhabitant. One interesting and rather unexpected confounding factor was gender. This study contributes to our understanding of the composition of the microbiota in early life and the succession process and the evolution of the microbial community as a function of time and events occurring during the first 6 months of life. Our results provide new insights that could be taken into consideration when selecting nutritional supplementation strategies to support the developing infant gut microbiome.

5 June 2014 in Pediatric Allergy and Immunology
Verified
Journal Article
Open access
PDF file
HWHarm Wopereis
Harm Wopereis
RORaish Oozeer
Raish Oozeer
KKKaren Knipping
Karen Knipping
CBClara Belzer
Clara Belzer
JKJan Knol
Jan Knol
The development of the intestinal microbiota in the first years of life is a dynamic process significantly influenced by early‐life nutrition. Pioneer bacteria colonizing the infant intestinal tract and the gradual diversification to a stable climax ecosystem plays a crucial role in establishing host–microbe interactions essential for optimal symbiosis. This colonization process and establishment of symbiosis may profoundly influence health throughout life. Recent developments in microbiologic cultivation‐independent methods allow a detailed view of the key players and factors involved in this process and may further elucidate their roles in a healthy gut and immune maturation. Aberrant patterns may lead to identifying key microbial signatures involved in developing immunologic diseases into adulthood, such as asthma and atopic diseases. The central role of early‐life nutrition in the developmental human microbiota, immunity, and metabolism offers promising strategies for prevention and treatment of such diseases. This review provides an overview of the development of the intestinal microbiota, its bidirectional relationship with the immune system, and its role in impacting health and disease, with emphasis on allergy, in early life.

1 January 2005 in Journal of Pediatric Gastroenterology and Nutrition
Verified
Journal Article
Closed access
JKJan Knol
Jan Knol
PSPetra Scholtens
Petra Scholtens
CKCorinna Kafka
Corinna Kafka
JSJochem Steenbakkers
Jochem Steenbakkers
SGSabine Gro
Sabine Gro
JWJohn Wells
John Wells