Positive and Negative Bacterial Associations Involving Dialister pneumosintes in Primary Endodontic Infections

2003 ◽  
Vol 29 (7) ◽  
pp. 438-441 ◽  
Author(s):  
J SIQUEIRAJR ◽  
I ROCAS
Author(s):  
Brenda P. F. A. Gomes ◽  
Juliana D. Bronzato ◽  
Rebecca F. Almeida-Gomes ◽  
Ericka T. Pinheiro ◽  
Ezilmara L. R. Sousa ◽  
...  

2003 ◽  
Vol 29 (12) ◽  
pp. 794-797 ◽  
Author(s):  
J BAUMGARTNER ◽  
S KHEMALEELAKUL ◽  
T XIA

2016 ◽  
Vol 144 (15) ◽  
pp. 3226-3236 ◽  
Author(s):  
J. E. NAVNE ◽  
M. L. BØRRESEN ◽  
H. C. SLOTVED ◽  
M. ANDERSSON ◽  
M. MELBYE ◽  
...  

SUMMARYThe incidence of childhood respiratory infections in Greenland is among the highest globally. We performed a population-based study of 352 Greenlandic children aged 0–6 years aiming to describe rates and risk factors for carriage of four key bacteria associated with respiratory infections, their antimicrobial susceptibility and inter-bacterial associations. Nasopharyngeal swabs were tested for Streptococcus pneumoniae grouped by serotypes included (VT) or not included (NVT) in the 13-valent pneumococcal conjugate vaccine, non-typable Haemophilus influenzae (NTHi), Staphylococcus aureus and Moraxella catarrhalis. S. pneumoniae was detected from age 2 weeks with a peak carriage rate of 60% in 2-year-olds. Young age and having siblings attending a daycare institution were associated with pneumococcal carriage. Overall co-colonization with ⩾2 of the studied bacteria was 52%. NTHi showed a positive association with NVT pneumococci and M. catarrhalis, respectively, M. catarrhalis was positively associated with S. pneumoniae, particular VT pneumococci, whereas S. aureus were negatively associated with NTHi and M. catarrhalis. Nasopharyngeal bacterial carriage was present unusually early in life and with frequent co-colonization. Domestic crowding increased odds of carriage. Due to important bacterial associations we suggest future surveillance of pneumococcal conjugate vaccine's impact on carriage in Greenland to also include other pathogens.


1983 ◽  
Vol 61 (3) ◽  
pp. 917-943 ◽  
Author(s):  
Silvano Scannerini ◽  
Paola Bonfante-Fasolo

Electron microscopy is a powerful tool in understanding functional mechanisms in symbiosis (i.e., recognition and transfer of nutrients between partners), but mycorrhizal associations are not yet so well known as host–pathogen and host – mutualistic bacterial associations. However, the study of mycorrhizal ultrastructure has provided some interesting information. In fact unknown symbionts can be recognized with electron microscopy and mycorrhizae can be classified according to a sequence linking intercellular and intracellular interactions between host and fungus. General conclusions can be drawn from this ultrastructural sequence. (i) The most significant cytological feature in mycorrhizae is the presence of an interface through which partners communicate along a vast surface area. This is the key area for symbiotic interactions (both recognition and nutrient transfer) and can vary a great deal mostly in intracellular interactions. (ii) The ultracytochemical aspects of those interfaces, mostly as regards the components of the interfacial matrix, appear quite different from those of host–pathogen associations and suggest a compatibility mechanism. (iii) As regards the transfer of nutrients, even though it has been claimed that transfer of nutrient in all intracellular interactions is achieved by a digestion mechanism of the fungus by the host, available ultrastructural data are not consistent with this hypothesis.


2007 ◽  
Vol 22 (6) ◽  
pp. 390-397 ◽  
Author(s):  
L. Sassone ◽  
R. Fidel ◽  
L. Figueiredo ◽  
S. Fidel ◽  
M. Faveri ◽  
...  

2010 ◽  
Vol 89 (9) ◽  
pp. 980-984 ◽  
Author(s):  
L. Li ◽  
W.W.L. Hsiao ◽  
R. Nandakumar ◽  
S.M. Barbuto ◽  
E.F. Mongodin ◽  
...  

2010 ◽  
Vol 43 (8) ◽  
pp. 637-645 ◽  
Author(s):  
N. Izutani ◽  
S. Imazato ◽  
Y. Noiri ◽  
S. Ebisu

2005 ◽  
Vol 73 (1) ◽  
pp. 268-276 ◽  
Author(s):  
Sung-Hoon Lee ◽  
Kack-Kyun Kim ◽  
Bong-Kyu Choi

ABSTRACT Treponema maltophilum and Treponema lecithinolyticum belong to the group IV oral spirochetes and are associated with endodontic infections, as well as periodontitis. Recently, the genes encoding the major surface proteins (Msps) of these bacteria (MspA and MspTL, respectively) were cloned and sequenced. The amino acid sequences of these proteins showed significant similarity. In this study we analyzed the functional role of these homologous proteins in human monocytic THP-1 cells and primary cultured periodontal ligament (PDL) cells using recombinant proteins. The complete genes encoding MspA and MspTL without the signal sequence were cloned into Escherichia coli by using the expression vector pQE-30. Fusion proteins tagged with N-terminal hexahistidine (recombinant MspA [rMspA] and rMspTL) were obtained, and any possible contamination of the recombinant proteins with E. coli endotoxin was removed by using polymyxin B-agarose. Flow cytometry showed that rMspA and rMspTL upregulated the expression of intercellular adhesion molecule 1 (ICAM-1) in both THP-1 and PDL cells. Expression of proinflammatory cytokines, such as interleukin-6 (IL-6) and IL-8, was also induced significantly in both cell types by the Msps, as determined by reverse transcription-PCR and an enzyme-linked immunosorbent assay, whereas IL-1β synthesis could be detected only in the THP-1 cells. The upregulation of ICAM-1, IL-6, and IL-8 was completely inhibited by pretreating the cells with an NF-κB activation inhibitor, l-1-tosylamido-2-phenylethyl chloromethyl ketone. This suggests involvement of NF-κB activation. The increased ICAM-1 and IL-8 expression in the THP-1 cells obtained with rMsps was not inhibited in the presence of the IL-1 receptor antagonist (IL-1ra), a natural inhibitor of IL-1. Our results show that the Msps of the group IV oral spirochetes may play an important role in amplifying the local immune response by continuous inflammatory cell recruitment and retention at an infection site by stimulation of expression of ICAM-1 and proinflammatory cytokines.


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