This study aims to develop a recombinase aided amplification(RAA)technology to de-tect porcine epidemic diarrhea virus(PEDV).A set of RAA primers and probes with high amplifi-cation efficiency and specificity was designed,specifically targeting the M gene.The amplification process was monitored in real-time using a fluorescent constant temperature detector to facilitate the rapid,sensitive,and specific detection of PEDV nucleic acids.The results showed that the es-tablished method exhibited excellent sensitivity,with a minimum detection limit of 8.86 × 101 copies/μL.Furthermore,the detection method has good specificity and reproducibility,with no cross-reactions observed with other porcine viruses such as transmissible gastroenteritis virus(TGE),porcine coronavirus,and porcine circovirus.The method also showed clear amplification curves at constant temperatures ranging from 37.0 to 41 ℃,highlighting its good temperature a-daptability.The establishment of fluorescent RAA technology for PEDV detection method provides a method for on-site rapid detection of PEDV.

This study aims to develop a recombinase aided amplification(RAA)technology to de-tect porcine epidemic diarrhea virus(PEDV).A set of RAA primers and probes with high amplifi-cation efficiency and specificity was designed,specifically targeting the M gene.The amplification process was monitored in real-time using a fluorescent constant temperature detector to facilitate the rapid,sensitive,and specific detection of PEDV nucleic acids.The results showed that the es-tablished method exhibited excellent sensitivity,with a minimum detection limit of 8.86 × 101 copies/μL.Furthermore,the detection method has good specificity and reproducibility,with no cross-reactions observed with other porcine viruses such as transmissible gastroenteritis virus(TGE),porcine coronavirus,and porcine circovirus.The method also showed clear amplification curves at constant temperatures ranging from 37.0 to 41 ℃,highlighting its good temperature a-daptability.The establishment of fluorescent RAA technology for PEDV detection method provides a method for on-site rapid detection of PEDV.

Sinus floor elevation was needed in 11 patients having 15 implant sites with the residual bone height (RBH) was less than 10 mm in the posterior maxillary region from Feb to May 2017. The RBH ranged from 3.10 to 8.34 mm [averaged (6.18±1.60) mm]. RBH<6 mm was observed in 40% implant sites (6 implant sites) and RBH≥6 mm was observed in 60% implant sites (9 implant sites). The thickness of the sinus floor membrane correspond to the implant site measured by cone beam CT (CBCT) ranged from 0.50 to 4.24 mm [averaged (1.21±0.92) mm]. Sequential drills with stops were used to perforate the cortical bone of the sinus floor firstly, then the transcrestal around detached sinus floor elevation technique (TADSFET) was carried with osteotomes. Anorganic bovine bone was used as the augmentation material.Fifteen implants were placed in 15 implant sites. CBCT pictures showed that there was a smooth and continuous tent-shaped apophysis on each lifted site and no air fluid level was observed in the sinus immediately after operation. The mean elevated height of the 15 implant sites was (7.83±1.57) mm (ranged from 5.94 to 11.01 mm). The mean follow-up time was 7.91 months (7-10 months). The survival rate was 100% during the follow up period.