1.Effects of vitamin C on the DNA of liver cells of the rats fed with low selenium and high cadmium fodder.
Yao-kui DUAN ; Wen-hua CAO ; Ai-guo LI
Chinese Journal of Applied Physiology 2006;22(3):332-342
Animal Feed
;
Animals
;
Ascorbic Acid
;
pharmacology
;
Cadmium
;
analysis
;
DNA
;
analysis
;
Hepatocytes
;
chemistry
;
Rats
;
Rats, Wistar
;
Selenium
;
analysis
3.Analysis of 105 Incarcerated Inmate's Death.
Yu-tao LI ; Li-juan SONG ; Ai-kui CAO ; Jian ZHOU ; Cai-rong GAO
Journal of Forensic Medicine 2015;31(5):366-368
OBJECTIVE:
To analyze the characteristics in the incarcerated inmate's death, investigate the main cause of death of the incarcerated inmate and provide some information for forensic investigation.
METHODS:
The cases from the forensic medical center of Shanxi Medical University from 2005 to 2013 were selected. The statistical analysis was performed by using the incarcerated inmate's gender, age, cause of death, manner of death, and disease as the markers.
RESULTS:
There were 100 men, 5 women in the 105 incarcerated inmates; the age range was from 16 to 65 years; Inmates were mostly died of natural diseases, mainly in the respiratory and cardiovascular diseases; the main unnatural death was suicide with a rate of 54.5%.
CONCLUSION
At present, most incarcerated inmate's death are due to natural diseases. The prison should improve incarcerated inmate's lives, work and health care conditions, and strengthen supervision of law enforcement.
Adolescent
;
Adult
;
Aged
;
Cardiovascular Diseases/mortality*
;
Cause of Death
;
Female
;
Humans
;
Male
;
Middle Aged
;
Prisoners/statistics & numerical data*
;
Prisons
;
Respiratory Tract Diseases/mortality*
;
Suicide
;
Young Adult
4.Clinical characteristics and drug sensitivity in children with invasive pneumococcal disease: a multicenter study.
Cai-Yun WANG ; Ying-Hu CHEN ; Xue-Jun CHEN ; Hong-Mei XU ; Chun-Mei JING ; Ji-Kui DENG ; Rui-Zhen ZHAO ; Hui-Ling DENG ; San-Cheng CAO ; Hui YU ; Chuan-Qing WANG ; Ai-Min WANG ; Ai-Wei LIN ; Shi-Fu WANG ; Qing CAO ; Xing WANG ; Ting ZHANG ; Hong ZHANG ; Jian-Hua HAO ; Cong-Hui ZHANG
Chinese Journal of Contemporary Pediatrics 2019;21(7):644-649
OBJECTIVE:
To study the clinical characteristics, drug sensitivity of isolated strains, and risk factors of drug resistance in children with invasive pneumococcal disease (IPD).
METHODS:
The clinical characteristics and drug sensitivity of the isolated strains of 246 hospitalized children with IPD in nine grade A tertiary children's hospitals from January 2016 to June 2018 were analyzed.
RESULTS:
Of the 246 children with IPD, there were 122 males and 124 females. Their ages ranged from 1 day to 14 years, and among them, 68 (27.6%) patients were less than 1 year old, 54 (22.0%) patients were 1 to 2 years old, 97 (39.4%) patients were 2 to 5 years old, and 27 (11.0%) patients were 5 to 14 years old. Pneumonia with sepsis was the most common infection type (58.5%, 144/246), followed by bloodstream infection without focus (19.9%, 49/246) and meningitis (15.0%, 37/246). Forty-nine (19.9%) patients had underlying diseases, and 160 (65.0%) had various risk factors for drug resistance. The isolated Streptococcus pneumoniae strains were 100% sensitive to vancomycin, linezolid, moxifloxacin, and levofloxacin, 90% sensitive to ertapenem, ofloxacin, and ceftriaxone, but had a low sensitivity to erythromycin (4.2%), clindamycin (7.9%), and tetracycline (6.3%).
CONCLUSIONS
IPD is more common in children under 5 years old, especially in those under 2 years old. Some children with IPD have underlying diseases, and most of the patients have various risk factors for drug resistance. Pneumonia with sepsis is the most common infection type. The isolated Streptococcus pneumoniae strains are highly sensitive to vancomycin, linezolid, moxifloxacin, levofloxacin, ertapenem, and ceftriaxone in children with IPD.
Anti-Bacterial Agents
;
Ceftriaxone
;
Child
;
Child, Preschool
;
Drug Resistance
;
Female
;
Humans
;
Infant
;
Male
;
Microbial Sensitivity Tests
;
Pneumococcal Infections
;
Streptococcus pneumoniae
5.Analysis of intestinal microbial diversity in Leopoldamys edwardsi based on illumina sequencing technique.
Duan Duan XUAN ; Yuan Li LI ; Guan Nan ZHANG ; Lin Wei DING ; Pei Pei CAO ; Rui Jie JIA ; Yu Ai ZHENG ; Xiao Jun ZHOU ; Liang Yuan PAN ; Shou Kui HU ; Li Na NIU
Chinese Journal of Preventive Medicine 2022;56(4):512-518
To explore the composition and diversity of the intestinal microflora of Leopoldamys edwardsi in Hainan Island. In November 2019, DNA was extracted from fecal samples of 25 adult Leopoldamys edwardsi (14 males and 11 females) in Hainan Island at the Joint Laboratory of tropical infectious diseases of Hainan Medical College and Hong Kong University. Based on the IonS5TMXL sequencing platform, single-end sequencing (Single-End) was used to construct a small fragment library for single-end sequencing. Based on Reads shear filtration and OTUs clustering. The species annotation and abundance analysis of OTUs were carried out by using mothur method and SSUrRNA database, and further conducted α diversity and β diversity analysis. A total of 1481842 high quality sequences, belonging to 14 Phyla, 85 families and 186 Genera, were obtained from 25 intestinal excrement samples of Leopoldamys edwardsi. At the level of phyla classification, the main core biota of the Leopoldamys edwardsi contained Firmicutes (46.04%),Bacteroidetes (25.34%), Proteobacteria (17.09%), Tenericutes (7.38%) and Actinobacteria (1.67%), these five phyla account for 97.52% of all phyla. The ratio of Helicobacter which occupied the largest proportion at the genus level was 12.44%, followed by Lactobacillus (11.39%), Clostridium (6.19%),Mycoplasma (4.23%) and Flavonifractor (3.52%). High throughput sequencing analysis showed that the intestinal flora of Leopoldamys edwardsi in Hainan Island was complex and diverse, which had the significance of further research.
Adult
;
Animals
;
Bacteria/genetics*
;
Feces/microbiology*
;
Female
;
Gastrointestinal Microbiome/genetics*
;
High-Throughput Nucleotide Sequencing
;
Humans
;
Intestines
;
Male
;
Murinae/genetics*