The sporadic emergence of New Delhi metallo-β-lactamase-1 (NDM-1)-producing Acinetobacter spp. has been reported in China; however, NDM-1-positive bacteria epidemics are rarely reported in intensive care units (ICUs) in China, or even in the world. During 15 months' surveillance Acinetobacter spp. isolated from patients, heathcare workers and surfaces of a Chinese ICU were screened for the bla(NDM-1) gene. A total of 27 of 3114 Acinetobacter spp. strains were NDM-1 positive and identified as A. pittii with sequence type 63 (ST63) by multilocus sequence typing. Of the 27 NDM-1-positive A. pittii strains, 22 were isolated from the ICU surfaces and grouped into a major clone A using pulsed-field gel electrophoresis typing, while the other five strains isolated from the patients were classified into three clones (A, B and C). The bla(NDM-1) gene was located on a 45-kb plasmid for all three A. pittii clones. The plasmid could be transferred to A. pittii and A. baumannii recipients at both 30 and 37°C but not to Escherichia coli J53. The plasmid could not be classified into any of the known plasmid incompatibility groups. The bla(NDM-1) region in the plasmid was flanked by two insertion sequence elements, ISAba125 and ISAba11, and no other carbapenemase gene was present in this NDM-1-positive A. pittii isolate. Thus, we present the first report on the transmission and characterization of NDM-1-producing A. pittii in an ICU in China as well as a novel bla(NDM-1) gene-bearing plasmid.

Chewing-side preference (CSP) may be associated with temporomandibular disorders. However, little information exists regarding whether CSP will lead to osseous changes of temporomandibular joint (TMJ) in asymptomatic participants. The aim of this study was to investigate the relationship between osseous morphology of TMJ in asymptomatic participants with CSP and without CSP. Of the 121 healthy dentate participants, 35 participants with left CSP, 38 with right CSP and other 48 without CSP were scanned by cone-beam computed tomography. The dimensions of the reconstructed images of opposing TMJs were compared. Statistical analyses were performed using spss 16.0 software. The results showed that there were no significant differences between the dimensions of bilateral structures of the TMJ (P1 > 0·05) in participants without CSP. However, the posterior-superior, posterior and lateral joint space of the preferred side were smaller than that of the unpreferred side in participants with CSP (P2 < 0·01) and bilateral TMJ in participants without CSP (P3 < 0·01). In addition, width of condylar neck of the unpreferred side both in sagittal and perpendicular to the long axis of condyle views was greater than that of the preferred side in participants with CSP (P2 < 0·01) and bilateral TMJ of participants without CSP (P4 < 0·01). Also, the inclination of articular eminence of the preferred side in view perpendicular to the long axis of condyle was less than that of the unpreferred side (P2 < 0·05). These findings suggest CSP affects osseous morphology of TMJ in asymptomatic participants.

The aim of this study was to investigate the activation characteristics of cerebral cortex in participants with CSP during rhythmic chewing movement. Sixteen right-handed participants with left (two males: 29·0 ± 8·4 years old, six females: 32·3 ± 4·8 years old) or right (four males: 31·0 ± 6·1 years old, four females: 30·8 ± 4·7 years old) CSP were scanned by functional magnetic resonance imaging during rhythmic chewing. The on-off sequence of scanning was 30 s of rhythmic chewing and 30 s of rest (off) a total of five times. The results showed that blood oxygen level-dependent signals in the contralateral (to the CSP) primary sensorimotor cortex increased more than in the ipsilateral primary sensorimotor cortex in participants with both left and right CSP (P ≤ 0·001). Moreover, the BOLD signal within the right substantia nigra of midbrain, brainstem was more significantly (P ≤ 0·001) activated than its left counterpart in participants with left CSP, while no activation was observed in those with right CSP. The similar activation of the cerebellum was in participants with right CSP. The inferior parietal lobule, inferior frontal gyrus and left insular cortex were significantly (P ≤ 0·001) activated in participants with CSP. These findings suggest a relationship between hemispheric dominance and CSP in the primary sensorimotor cortex responsible for rhythmic chewing movement. The brainstem and the cerebellum might also play important role in the regulation of CSP. Furthermore, the IFG, IPL and insular may contribute to higher cognitive information processing for participants with CSP.

The aim of this study is to investigate the accuracy and adequacy of the Pipelle endometrial sampler for endometrial biopsy as compared with those of conventional dilatation and curettage (D&C). A total of 245 patients subject to endometrial biopsy were included in this study. We have shown that the failure rates with D&C and Pipelle were 7.75% and 8.98%, respectively, without statistical difference. Additionally, the obtained specimen quality and accurate diagnosis of various diseases using the two methods had no significant statistical differences. Furthermore, patients experienced less pain when Pipelle sampler was used than D&C. Therefore, Pipelle sampler is effective in obtaining adequate endometrial tissue for histodiagnosis, and is applicable in most of the cases for Chinese endometrial biopsy.

The aim of this review of the literature was to assess the biological effects of occlusal trauma on the stomatognathic system focusing on animal studies. However, there are no conclusive explanations on the association between occlusal trauma and disease of the stomatognathic system. A literature survey was performed using the Medline database, covering the period from 1967 to 2012. Over 300 abstracts were reviewed, and 70 manuscripts were selected. Additional references from citations within the articles were obtained, and current textbooks were also used. This review does not include the effects of occlusal trauma on dental implants or dental prostheses/appliances. A total of 70 full articles were included for the final analysis. The selected 70 articles were classified into the following five categories, including the effects of occlusal trauma on the pulp tissues, periodontal tissues, masticatory muscle, temporomandibular joint (TMJ) and central nervous system (CNS). It was demonstrated that occlusal trauma caused a variety of harmful biological effects on stomatognathic system. Additionally, occlusal trauma could lead to some pain substance changes in the pulp, periodontal tissues, masticatory muscle, TMJ and CNS, which was possibly related to the peripheral and the central neuronal sensitisation. However, these findings demonstrate that there are remaining disagreements by various authors. More randomised trials are needed to validate these effects.

Close talk between inflammatory mediators and immunological cytokines has been discovered and reported. In this study, the role of nuclear factor of activated T cell-2 (NFAT2) in regulation of high mobility group box-l (HMGBl) release was investigated. THP-l cell and HEK293T cell were incubated and stimulated by lipopolysaccharide (LPS). Firstly, binding site between HMGBI and NFAT2 was identified by co-immunoprecipitation (IP). Box A, Box Band CT domain of HMGBI were constructed, as well as ReI-homology-domain (RHD), pre-RHD and pro-RHD ofNFAT2. THP-l cell was harvested, cell lysate and culture medium were collected at appointed times. Binding between HMGBI and NFAT2 was measured, HMGBI protein level in culture medium was analyzed at the same time. Secondly, the role of NFAT2 in regulating HMGBI release was investigated. When THP-l cell was cultured for 24 h, HMGBI protein level was measured at appointed times with or without siRNA to inhibit NFAT2 expression. Our data show that HMGBI bound to NFAT2 in THP-l cell cytoplasm. Further experiments showed that box B domain of HMGBI could bind to pre-RHD of NFAT2. After stimulation by LPS, interaction between HMGBI and NFAT2 was discovered decreasing gradually. However, HMGBI protein level increased in culture medium at the same time. Furthermore, HMGBI release could be enhanced by NFAT2 inhibition. Taken together, release of HMGBI could be regulated by NFAT2 in human monocytes. HMGB 1 is not only a "late" inflammatory mediator, but also plays an important role in immune regulation. HMGB 1 could be secreted positively by activated inflammatory cells or be released negatively by necrotic cells. Early elevation «6 hours) of serum HMGBllevel in septic patients was mainly caused by HMGBI initiative secretion of activated inflammatory cells. HMGB 1 level would peak again in a later period (> 12 hours) which was caused by increasing expression and release of HMGB 1 in inflammatory cells.Extracellular HMGB 1 is potent in initiating immune responses by inducing antigen-presenting cell activation and mediating Thl polarization (1-3). Our previous study found Nuclear factor of activated T cells, cytoplasmic 1 (NFAT2) was one of the

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