scholarly journals Intestinal Integrity and Akkermansia muciniphila, a Mucin-Degrading Member of the Intestinal Microbiota Present in Infants, Adults, and the Elderly

2007 ◽  
Vol 73 (23) ◽  
pp. 7767-7770 ◽  
Author(s):  
M. Carmen Collado ◽  
Muriel Derrien ◽  
Erika Isolauri ◽  
Willem M. de Vos ◽  
Seppo Salminen
Keyword(s):  
Early Life ◽  
Intestinal Tract ◽  
The Elderly ◽  
Pcr Analysis ◽  
Rrna Gene ◽  
Akkermansia Muciniphila ◽  
Intestinal Integrity ◽  
The 16S Rrna Gene ◽  
Human Intestinal Tract

ABSTRACT Fluorescence in situ hybridization and real-time PCR analysis targeting the 16S rRNA gene of Akkermansia muciniphila were performed to determine its presence in the human intestinal tract. These techniques revealed that an A. muciniphila-like bacterium is a common member of the human intestinal tract and that its colonization starts in early life and develops within a year to a level close to that observed in adults (108 cells/g) but decreases (P < 0.05) in the elderly.

scholarly journals Akkermansia muciniphila in the Human Gastrointestinal Tract: When, Where, and How?

2018 ◽  
Vol 6 (3) ◽  
pp. 75 ◽  
Author(s):  
Sharon Geerlings ◽  
Ioannis Kostopoulos ◽  
Willem de Vos ◽  
Clara Belzer
Keyword(s):  
Human Milk ◽  
Intestinal Tract ◽  
16S Rrna Sequence ◽  
Akkermansia Muciniphila ◽  
Intestinal Integrity ◽  
Disease States ◽  
Degrading Bacterium ◽  
Mucosal Layer ◽  
Breast Fed ◽  
Human Intestinal Tract

Akkermansia muciniphila is a mucin-degrading bacterium of the phylum Verrucomicrobia. Its abundance in the human intestinal tract is inversely correlated to several disease states. A. muciniphila resides in the mucus layer of the large intestine, where it is involved in maintaining intestinal integrity. We explore the presence of Akkermansia-like spp. based on its 16S rRNA sequence and metagenomic signatures in the human body so as to understand its colonization pattern in time and space. A. muciniphila signatures were detected in colonic samples as early as a few weeks after birth and likely could be maintained throughout life. The sites where Akkermansia-like sequences (including Verrucomicrobia phylum and/or Akkermansia spp. sequences found in the literature) were detected apart from the colon included human milk, the oral cavity, the pancreas, the biliary system, the small intestine, and the appendix. The function of Akkermansia-like spp. in these sites may differ from that in the mucosal layer of the colon. A. muciniphila present in the appendix or in human milk could play a role in the re-colonization of the colon or breast-fed infants, respectively. In conclusion, even though A. muciniphila is most abundantly present in the colon, the presence of Akkermansia-like spp. along the digestive tract indicates that this bacterium might have more functions than those currently known.

scholarly journals The Mucin Degrader Akkermansia muciniphila Is an Abundant Resident of the Human Intestinal Tract

2007 ◽  
Vol 74 (5) ◽  
pp. 1646-1648 ◽  
Author(s):  
Muriel Derrien ◽  
M. Carmen Collado ◽  
Kaouther Ben-Amor ◽  
Seppo Salminen ◽  
Willem M. de Vos
Keyword(s):  
In Situ Hybridization ◽  
16S Rrna ◽  
Fluorescent In Situ Hybridization ◽  
Intestinal Tract ◽  
Akkermansia Muciniphila ◽  
Human Intestinal Tract

ABSTRACT A 16S rRNA-targeted probe, MUC-1437, was designed and validated in order to determine the presence and numbers of cells of Akkermansia muciniphila, a mucin degrader, in the human intestinal tract. As determined by fluorescent in situ hybridization, A. muciniphila accounted more than 1% of the total fecal cells and was shown to be a common bacterial component of the human intestinal tract.

scholarly journals A Differential Metabarcoding Approach to Describe Taxonomy Profiles of Bacteria and Archaea in the Saltern of Margherita di Savoia (Italy)

2020 ◽  
Vol 8 (6) ◽  
pp. 936 ◽  
Author(s):  
Claudia Leoni ◽  
Mariateresa Volpicella ◽  
Bruno Fosso ◽  
Caterina Manzari ◽  
Elisabetta Piancone ◽  
...  
Keyword(s):  
Ecological Model ◽  
Salinity Range ◽  
Rrna Gene ◽  
Hypervariable Regions ◽  
Cell Counts ◽  
Precious Resource ◽  
Catalyzed Reporter Deposition ◽  
Card Fish ◽  
The 16S Rrna Gene

Microorganisms inhabiting saline environments are an interesting ecological model for the study of the adaptation of organisms to extreme living conditions and constitute a precious resource of enzymes and bioproducts for biotechnological applications. We analyzed the microbial communities in nine ponds with increasing salt concentrations (salinity range 4.9–36.0%) of the Saltern of Margherita di Savoia (Italy), the largest thalassohaline saltern in Europe. A deep-metabarcoding NGS procedure addressing separately the V5-V6 and V3-V4 hypervariable regions of the 16S rRNA gene of Bacteria and Archaea, respectively, and a CARD-FISH (catalyzed reporter deposition fluorescence in situ hybridization) analysis allowed us to profile the dynamics of microbial populations at the different salt concentrations. Both the domains were detected throughout the saltern, even if the low relative abundance of Archaea in the three ponds with the lowest salinities prevented the construction of the relative amplicon libraries. The highest cell counts were recorded at 14.5% salinity for Bacteria and at 24.1% salinity for Archaea. While Bacteria showed the greatest number of genera in the first ponds (salinity range 4.9–14.5%), archaeal genera were more numerous in the last ponds of the saltern (salinity 24.1–36.0%). Among prokaryotes, Salinibacter was the genus with the maximum abundance (~49% at 34.6% salinity). Other genera detected at high abundance were the archaeal Haloquadratum (~43% at 36.0% salinity) and Natronomonas (~18% at 13.1% salinity) and the bacterial “Candidatus Aquiluna” (~19% at 14.5% salinity). Interestingly, “Candidatus Aquiluna” had not been identified before in thalassohaline waters.

scholarly journals PCR Analysis of the Distribution of Unicellular Cyanobacterial Diazotrophs in the Arabian Sea

2004 ◽  
Vol 70 (12) ◽  
pp. 7355-7364 ◽  
Author(s):  
Sophie L. Mazard ◽  
Nicholas J. Fuller ◽  
Karen M. Orcutt ◽  
Oliver Bridle ◽  
Dave J. Scanlan
Keyword(s):  
Arabian Sea ◽  
Marine Diatom ◽  
Pcr Analysis ◽  
Oligonucleotide Primer ◽  
Rrna Gene ◽  
Key Factor ◽  
Subsurface Waters ◽  
Reverse Primer ◽  
The 16S Rrna Gene ◽  
Forward Primer

ABSTRACT An oligonucleotide primer, NITRO821R, targeting the 16S rRNA gene of unicellular cyanobacterial N2 fixers was developed based on newly derived sequences from Crocosphaera sp. strain WH 8501 and Cyanothece sp. strains WH 8902 and WH 8904 as well as several previously described sequences of Cyanothece sp. and sequences of intracellular cyanobacterial symbionts of the marine diatom Climacodium frauenfeldianum. This oligonucleotide is specific for the targeted organisms, which represent a well-defined phylogenetic lineage, and can detect as few as 50 cells in a standard PCR when it is used as a reverse primer together with the cyanobacterium- and plastid-specific forward primer CYA359F (U. Nübel, F. Garcia-Pichel, and G. Muyzer, Appl. Environ. Microbiol. 63:3327-3332, 1997). Use of this primer pair in the PCR allowed analysis of the distribution of marine unicellular cyanobacterial diazotrophs along a transect following the 67°E meridian from Victoria, Seychelles, to Muscat, Oman (0.5°S to 26°N) in the Arabian Sea. These organisms were found to be preferentially located in warm (>29°C) oligotrophic subsurface waters between 0 and 7°N, but they were also found at a station north of Oman at 26°N, 56°35′E, where similar water column conditions prevailed. Slightly cooler oligotrophic waters (<29°C) did not contain these organisms or the numbers were considerably reduced, suggesting that temperature is a key factor in dictating the abundance of this unicellular cyanobacterial diazotroph lineage in marine environments.

Anammox bacteria detected in fish intestinal tract systems

2016 ◽  
Vol 1 (1) ◽  
pp. 13 ◽  
Author(s):  
Ho Wang Chan ◽  
Han Meng ◽  
Ji-Dong Gu
Keyword(s):  
Intestinal Tract ◽  
Eating Habits ◽  
Anthropogenic Pollution ◽  
Living Conditions ◽  
Anammox Bacteria ◽  
Rrna Gene ◽  
Animal System ◽  
Wastewater Pollution ◽  
Global Nitrogen Cycle ◽  
The 16S Rrna Gene

Anammox bacteria serve an important ecological role in the global nitrogen cycle, enabling the coupling of ammonium and nitrite to yield dinitrogen gas (N2) under anoxic conditions. Based on PCR amplifications of genomic DNA and analysis of the 16S rRNA gene sequence, anammox bacteria was found in intestinal tracts of two types of fish, Siganus fuscescens and Mugil cephalus. Anammox bacteria identified in these fish belonged to the genera Brocadia and Kuenenia, suggesting that the living conditions of S. fuscescens and M. cephalus were under significant influence of wastewater pollution. Our results showed an association between the existence of anammox bacteria in fish intestinal tracts and sediment- or mud-eating habits of the fish involved. The presence of anammox bacteria in an animal system would provide a more comprehensive understanding on ecophysiological characteristics and distribution of anammox bacteria. This discovery might also provide useful information about the living conditions of fish, serving as an environmental indicator of anthropogenic pollution.

scholarly journals Demonstration of Bartonella grahamii DNA in Ocular Fluids of a Patient with Neuroretinitis

1999 ◽  
Vol 37 (12) ◽  
pp. 4034-4038 ◽  
Author(s):  
F. T. Kerkhoff ◽  
A. M. C. Bergmans ◽  
A. van der Zee ◽  
A. Rothova
Keyword(s):  
Gene Sequence ◽  
Dna Analysis ◽  
Behavioral Changes ◽  
Pcr Analysis ◽  
Rrna Gene ◽  
Rrna Gene Sequence ◽  
Pcr Product ◽  
Immunodeficiency Virus ◽  
Laboratory Features ◽  
The 16S Rrna Gene

We describe the clinical and laboratory features of a 55-year-old human immunodeficiency virus-negative female patient who presented with bilateral intraocular inflammatory disease (neuroretinitis type) and behavioral changes caused by a Bartonella grahamiiinfection. Diagnosis was based on the PCR analysis of DNA extracted from the intraocular fluids. DNA analysis of the PCR product revealed a 100% identity with the 16S rRNA gene sequence of B. grahamii. The patient was successfully treated with doxycycline (200 mg/day) and rifampin (600 mg/day) for 4 weeks. This is the first report that demonstrates the presence of a Bartonellaspecies in the intraocular fluids of a nonimmunocompromised patient and that indicates that B. grahamii is pathogenic for humans.

Ultrastructural and molecular characterization of endosymbionts of the reed beetle genusMacroplea(Chrysomelidae, Donaciinae), and proposal of “CandidatusMacropleicola appendiculatae” and “CandidatusMacropleicola muticae”

2009 ◽  
Vol 55 (11) ◽  
pp. 1250-1260 ◽  
Author(s):  
Gregor Kölsch ◽  
Corinna Matz-Grund ◽  
Bo V. Pedersen
Keyword(s):  
Phylogenetic Analysis ◽  
16S Rrna ◽  
Fluorescent In Situ Hybridization ◽  
Malpighian Tubules ◽  
Rrna Gene ◽  
Beetle Species ◽  
Bacterial Symbionts ◽  
The 16S Rrna Gene

Intracellular bacterial symbionts are known from various insect groups, particularly from those feeding on unbalanced diets, where the bacteria provide essential nutrients to the host. In the case of reed beetles (Coleoptera: Chrysomelidae, Donaciinae), however, the endosymbionts appear to be associated with specialized “glands” that secrete a material used for the beetles’ unusual water-tight cocoon. These glands were discovered over a century ago, but the bacteria they contain have yet to be characterized and placed in a phylogenetic context. Here, we describe the ultrastructure of two endosymbiotic species (“ Candidatus Macropleicola appendiculatae” and “ Candidatus Macropleicola muticae”) that reside in cells of the Malpighian tubules of the reed beetle species Macroplea appendiculata and Macroplea mutica , respectively. Fluorescent in situ hybridization using oligonucleotides targeting the 16S rRNA gene specific to Macroplea symbionts verified the localization of the symbionts in these organs. Phylogenetic analysis of 16S rRNA placed “Candidatus Macropleicola” in a clade of typically endosymbiotic Enterobacteriaceae (γ-proteobacteria). Finally, we discuss the evidence available for the hypothesis that the beetle larvae use a secretion produced by the bacteria for the formation of an underwater cocoon.

scholarly journals Feasibility of Transferring Fluorescent In Situ Hybridization Probes to an 18S rRNA Gene Phylochip and Mapping of Signal Intensities

2008 ◽  
Vol 74 (9) ◽  
pp. 2814-2821 ◽  
Author(s):  
Katja Metfies ◽  
Linda K. Medlin
Keyword(s):  
In Situ Hybridization ◽  
Secondary Structure ◽  
16S Rrna ◽  
Fluorescent In Situ Hybridization ◽  
18S Rrna ◽  
18S Rrna Gene ◽  
Rrna Gene ◽  
Rrna Molecule ◽  
The 16S Rrna Gene

ABSTRACT DNA microarray technology offers the possibility to analyze microbial communities without cultivation, thus benefiting biodiversity studies. We developed a DNA phylochip to assess phytoplankton diversity and transferred 18S rRNA probes from dot blot or fluorescent in situ hybridization (FISH) analyses to a microarray format. Similar studies with 16S rRNA probes have been done determined that in order to achieve a signal on the microarray, the 16S rRNA molecule had to be fragmented, or PCR amplicons had to be <150 bp in length to minimize the formation of a secondary structure in the molecule so that the probe could bind to the target site. We found different results with the 18S rRNA molecule. Four out of 12 FISH probes exhibited false-negative signals on the microarray; eight exhibited strong but variable signals using full-length 18S RNA molecules. A systematic investigation of the probe's accessibility to the 18S rRNA gene was made using Prymenisum parvum as the target. Fourteen additional probes identical to this target covered the regions not tested with existing FISH probes. Probes with a binding site in the first 900 bp of the gene generated positive signals. Six out of nine probes binding in the last 900 bp of the gene produced no signal. Our results suggest that although secondary structure affected probe binding, the effect is not the same for the 18S rRNA gene and the 16S rRNA gene. For the 16S rRNA gene, the secondary structure is stronger in the first half of the molecule, whereas in the 18S rRNA gene, the last half of the molecule is critical. Probe-binding sites within 18S rRNA gene molecules are important for the probe design for DNA phylochips because signal intensity appears to be correlated with the secondary structure at the binding site in this molecule. If probes are designed from the first half of the 18S rRNA molecule, then full-length 18S rRNA molecules can be used in the hybridization on the chip, avoiding the fragmentation and the necessity for the short PCR amplicons that are associated with using the 16S rRNA molecule. Thus, the 18S rRNA molecule is a more attractive molecule for use in environmental studies where some level of quantification is desired. Target size was a minor problem, whereas for 16S rRNA molecules target size rather than probe site was important.

scholarly journals The Dehalococcoides Population in Sediment-Free Mixed Cultures Metabolically Dechlorinates the Commercial Polychlorinated Biphenyl Mixture Aroclor 1260

2007 ◽  
Vol 73 (8) ◽  
pp. 2513-2521 ◽  
Author(s):  
Donna L. Bedard ◽  
Kirsti M. Ritalahti ◽  
Frank E. Löffler
Keyword(s):  
Polychlorinated Biphenyl ◽  
Anaerobic Bacteria ◽  
Pcr Analysis ◽  
Rrna Gene ◽  
Reductive Dehalogenase ◽  
Microbial Reductive Dechlorination ◽  
Pcb Dechlorination ◽  
Bacterial Groups ◽  
Polychlorinated Biphenyl Mixture

ABSTRACT Microbial reductive dechlorination of commercial polychlorinated biphenyl (PCB) mixtures (e.g., Aroclors) in aquatic sediments is crucial to achieve detoxification. Despite extensive efforts over nearly two decades, the microorganisms responsible for Aroclor dechlorination remained elusive. Here we demonstrate that anaerobic bacteria of the Dehalococcoides group derived from sediment of the Housatonic River (Lenox, MA) simultaneously dechlorinate 64 PCB congeners carrying four to nine chlorines in Aroclor 1260 in the sediment-free JN cultures. Quantitative real-time PCR showed that the Dehalococcoides cell titer in JN cultures amended with acetate and hydrogen increased from 7.07 × 106 ± 0.42 × 106 to 1.67 × 108 ± 0.04 × 108 cells/ml, concomitant with a 64.2% decrease of the PCBs with six or more chlorines in Aroclor 1260. No Dehalococcoides growth occurred in parallel cultures without PCBs. Aroclor 1260 dechlorination supported the growth of 9.25 × 108 ± 0.04 × 108 Dehalococcoides cells per μmol of chlorine removed. 16S rRNA gene-targeted PCR analysis of known dechlorinators (i.e., Desulfitobacterium, Dehalobacter, Desulfuromonas, Sulfurospirillum, Anaeromyxobacter, Geobacter, and o-17/DF-1-type Chloroflexi organisms) ruled out any involvement of these bacterial groups in the dechlorination. Our results suggest that the Dehalococcoides population present in the JN cultures also catalyzes in situ dechlorination of Aroclor 1260 in the Housatonic River. The identification of Dehalococcoides organisms as catalysts of extensive Aroclor 1260 dechlorination and our ability to propagate the JN cultures under defined conditions offer opportunities to study the organisms' ecophysiology, elucidate nutritional requirements, identify reductive dehalogenase genes involved in PCB dechlorination, and design molecular tools required for bioremediation applications.

scholarly journals Nocturnal Production of Endospores in Natural Populations of Epulopiscium-Like Surgeonfish Symbionts

2005 ◽  
Vol 187 (21) ◽  
pp. 7460-7470 ◽  
Author(s):  
Joseph F. Flint ◽  
Dan Drzymalski ◽  
W. Linn Montgomery ◽  
Gordon Southam ◽  
Esther R. Angert
Keyword(s):  
Intestinal Tract ◽  
Dipicolinic Acid ◽  
Phylogenetic Analyses ◽  
Natural Populations ◽  
Rrna Gene ◽  
Gram Positive Bacteria ◽  
Close Relationship ◽  
Close Relatives ◽  
In Situ Hybridizations

ABSTRACT Prior studies have described a morphologically diverse group of intestinal microorganisms associated with surgeonfish. Despite their diversity of form, 16S rRNA gene surveys and fluorescent in situ hybridizations indicate that these bacteria are low-G+C gram-positive bacteria related to Epulopiscium spp. Many of these bacteria exhibit an unusual mode of reproduction, developing multiple offspring intracellularly. Previous reports have suggested that some Epulopiscium-like symbionts produce dormant or phase-bright intracellular offspring. Close relatives of Epulopiscium, such as Metabacterium polyspora and Clostridium lentocellum, are endospore-forming bacteria, which raises the possibility that the phase-bright offspring are endospores. Structural evidence and the presence of dipicolinic acid demonstrate that phase-bright offspring of Epulopiscium-like bacteria are true endospores. In addition, endospores are formed as part of the normal daily life cycle of these bacteria. In the populations studied, mature endospores were seen only at night and the majority of cells in a given population produced one or two endospores per mother cell. Phylogenetic analyses confirmed the close relationship between the endospore-forming surgeonfish symbionts characterized here and previously described Epulopiscium spp. The broad distribution of endospore formation among the Epulopiscium phylogenetic group raises the possibility that sporulation is a characteristic of the group. We speculate that spore formation in Epulopiscium-like symbionts may be important for dispersal and may also enhance survival in the changing conditions of the fish intestinal tract.

Sign in / Sign up

Export Citation Format

Share Document