Acinetobacter baumannii is considered to be a worldwide threat to public health due to its high antimicrobial resistance rates and the severe infections it can cause. Little is known about this pathogen’s resistance in Mongolia. This report aims to describe the antimicrobial resistance profile of A. baumannii at a tertiary hospital in Mongolia. The cross-sectional analysis was conducted at the tertiary care laboratory hospital in the First Central Hospital of Mongolia from 2013.01 to 2013.12 and from 2020.01 to 2020.12.
A total of 141 in 2013, 227 in 2020 consecutive microbiological reports were analyzed. A. baumannii was isolated. Epidemiological and microbiological data, including the isolation setting and patient information, were recorded. Prevalence of multi-drug and extensive-drug resistance was assessed according to international standards.
The median age of individuals was 22 years (2 – 35 years); female was the predominant gender (53%). The hospital’s intensive care units had the highest number of isolates (n = 226). The most frequent specimen from which A. baumannii was isolated was secretion of respiratory tract (n = 119). Resistance to carbapenems was reported to be 35% among the isolates (n = 115) in 2013 and 74.69% (n=135) respectively. This report reveals the threat of this pathogen to public health in Mongolia and appeals for antibiotic stewardship programs throughout all tertiary hospitals and other hospitals.

Introduction: Base excision repair (BER) is mainly responsible for the correction of small base changes of DNA damage. BER pathway involved many enzymes including OGG1 and XRCC1. The defective DNA repair is associated with an increased risk of various cancers including hematologic malignancies-leukemia and myelodysplastic syndrome (MDS). However, it is deniably these polymorphisms alter the susceptibility and clinical outcome of MDS patients. The aim: This study was to evaluate the impact of polymorphisms in gene encoding one protein of BER system: XRCC1 Arg399Gln in MDS and healthy population. Methods: In this study, we recruited 60 health control group [median 47.9 years, 9 MDS subjects [median 56.6 years] were included in this study. Genotyping was carried out by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. Allele and genotype frequencies were calculated by direct counting. Result: The frequencies of genotypes of XRCC1 Arg399Gln were as follows: Arg /Arg 1 (11%), Arg/Gln 6 (66%), Gln/Gln 2 (22%) in MDS and Arg /Arg 18.4%, Arg/Gln40%, Gln/Gln41.6% in health control for XRCC1 Arg399Gln. The result revealed that genotypes Arg399Gln increased the risk of MDS In conclusion this study is the first to analyze XRCC1 SNPs and their associated risk of MDS in Mongolian samples. To fully understand the role of DNA damage and DNA repair in the MDS, prospective studies are needed and other genes (OGG1 Ser326Cys, MUTYH Gln324His, APE Asp148Glu) of base excision repair pathway should be analyzed.