Whole genome-based antimicrobial resistance and virulence profiling of Staphylococcus aureus isolates from chronic leg ulcer patients in Kilimanjaro, Tanzania

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Infection Genetics and Evolution Pub Date : 2024-06-28 DOI:10.1016/j.meegid.2024.105631
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Abstract

Background

Chronic leg ulcers are hard to treat and can be a burden, particularly in resource-limited settings where diagnosis is a challenge. Staphylococcus aureus is among the common bacteria isolated from chronic wounds with a great impact on wound healing, particularly in patients with co-morbidities. Antimicrobial resistance genes and virulence factors in Staphylococcus aureus isolates were assessed to support healthcare professionals to make better therapeutic choices, and importantly to curb the development and spread of antibiotic resistance.

Methods

A cross-sectional study involved both inpatients and outpatients with chronic leg ulcers was conducted from August 2022 to April 2023 in 2 health facilities in Kilimanjaro region in Tanzania. Antimicrobial susceptibility testing was done using the disk diffusion method. Further, whole genome sequencing was performed to study the genotypic characteristics of the isolates.

Results

A total of 92 participants were recruited in which 9 participants were only positive for 10 Staphylococcus aureus isolates upon culture. Five STs among 9 isolates were identified. Most of them belonged to ST8 (44%), with 1 isolate does not belong to any ST. Additionally, 50% of the isolates were methicillin-resistant Staphylococcus aureus (MRSA). All S. aureus isolates had almost similar virulence factors such as hemolysin, proteases and evasions that promote toxin production, protease production and host immune evasion respectively. Moreover, all mecA positive S. aureus isolates were phenotypically susceptible to cefoxitin.

Conclusion

Presence of mecA positive S. aureus isolates which are also phenotypically susceptible to cefoxitin implies the possibility of classifying MRSA as MSSA. This may result in the possible emergence of highly cefoxitin - resistant strains in health care and community settings when subsequently exposed to beta-lactam agents. Therefore, combination of whole genome sequencing and conventional methods is important in assessing bacterial resistance and virulence to improve management of patients.

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基于全基因组的坦桑尼亚乞力马扎罗山慢性腿部溃疡患者金黄色葡萄球菌耐药性和毒力分析。
背景:慢性腿部溃疡难以治疗,是一种负担,尤其是在资源有限的环境中,诊断是一项挑战。金黄色葡萄球菌是从慢性伤口中分离出来的常见细菌之一,对伤口愈合有很大影响,尤其是对合并有其他疾病的患者。我们对分离出的金黄色葡萄球菌的抗菌药耐药性基因和毒力因子进行了评估,以帮助医护人员做出更好的治疗选择,更重要的是遏制抗生素耐药性的发展和蔓延:方法:2022 年 8 月至 2023 年 4 月,在坦桑尼亚乞力马扎罗地区的两家医疗机构开展了一项横断面研究,涉及慢性腿部溃疡的住院病人和门诊病人。抗菌药物药敏试验采用盘扩散法进行。此外,还进行了全基因组测序,以研究分离物的基因型特征:结果:共招募了 92 名参与者,其中 9 名参与者的 10 株金黄色葡萄球菌分离物经培养后仅呈阳性。9 个分离株中有 5 个 ST。其中大部分属于 ST8(44%),1 个分离株不属于任何 ST。此外,50%的分离物为耐甲氧西林金黄色葡萄球菌(MRSA)。所有分离出的金黄色葡萄球菌都具有几乎相似的毒力因子,如溶血素、蛋白酶和回避因子,它们分别促进毒素的产生、蛋白酶的产生和宿主免疫回避。此外,所有 mecA 阳性的金黄色葡萄球菌分离株在表型上都对头孢西丁敏感:结论:存在对头孢西丁表型敏感的 mecA 阳性金黄色葡萄球菌分离株意味着有可能将 MRSA 归类为 MSSA。这可能会导致在医疗保健和社区环境中出现对头孢西丁高度耐药的菌株,随后再接触β-内酰胺类药物。因此,结合全基因组测序和传统方法来评估细菌的耐药性和毒力对改善患者管理非常重要。
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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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