Synovial Fluid Mediated Aggregation of Clinical Strains of Four Enterobacterial Species.
Synovial Fluid Mediated Aggregation of Clinical Strains of Four Enterobacterial Species.
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DOI:
10.1007/5584_2020_573
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发表时间:
2021
影响因子:
--
通讯作者:
Esteban J
中科院分区:
文献类型:
--
作者:
Macias-Valcayo A;Staats A;Aguilera-Correa JJ;Brooks J;Gupta T;Dusane D;Stoodley P;Esteban J
Septic arthritis and prosthetic joint infection (PJI) are conditions commonly associated with Gram-positive cocci, however, a drastic increase in cases derived from enterobacterial species has recently been observed. Recently it has been reported by multiple groups that staphylococci rapidly form free-floating aggregates in the presence of synovial fluid. These aggregates are comparatively more resistant to antimicrobial challenge than their planktonic counterparts, and thus may play a role in the pathogenesis of joint infection. While staphylococcal aggregates have been the primary focus of interest in the field, it is unclear just how widespread synovial fluid mediated aggregation (SFMA) is in Gram negative enterobacteria (GNE). Through this work we have evaluated SFMA in clinical GNE isolated from PJIs. Two PJI clinical strains each of Enterobacter cloacae, Escherichia coli, Klebsiella pneumonia and Proteus mirabilis strains representing a range of antibiotic susceptibilities were exposed to 10% bovine synovial fluid supernatant (BSF) using a relatively simple, quick semi-quantitative method using an imaging plate reader. BSF stimulated aggregation within 0.5 hr both strains of E. cloacae and P. mirabilis and one strain of E.coli. In one strain of P. mirabilis and E.coli, the size of the aggregates significantly increased from 0.5 to 2 hr exposure. In contrast, neither K. pneumoniae strain aggregated in BSF. These preliminary findings show that aggregation can occur quickly in GNE, but the extent appears strain and species specific. Further work is required to assess the impact of SFMA on antibiotic tolerance, host innate immunity and the establishment of biofilms.
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DOI:
10.1016/j.ymthe.2017.06.021
发表时间:
2017-09-06
期刊:
Molecular therapy : the journal of the American Society of Gene Therapy
影响因子:
--
作者:
Howlin RP;Cathie K;Hall-Stoodley L;Cornelius V;Duignan C;Allan RN;Fernandez BO;Barraud N;Bruce KD;Jefferies J;Kelso M;Kjelleberg S;Rice SA;Rogers GB;Pink S;Smith C;Sukhtankar PS;Salib R;Legg J;Carroll M;Daniels T;Feelisch M;Stoodley P;Clarke SC;Connett G;Faust SN;Webb JS
通讯作者:
Webb JS
影响因子:
14.2
作者:
Rodriguez-Pardo, D.;Pigrau, C.;Ariza, J.
通讯作者:
Ariza, J.
影响因子:
4.4
作者:
Nair, Rajeshwari;Schweizer, Marin L.;Singh, Namrata
通讯作者:
Singh, Namrata
影响因子:
2.7
作者:
Chiu, Li Qi;Wang, Wilson
通讯作者:
Wang, Wilson
影响因子:
14.2
作者:
Benito, N.;Franco, M.;Ariza, J.
通讯作者:
Ariza, J.