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对从印度尼西亚望加锡伤寒热患者分离出的伤寒杆菌血清型中多药耐药H58基因存在情况的分析。

Analysis of existence of multidrug-resistant H58 gene in serovar Typhi isolated from typhoid fever patients in Makassar, Indonesia.

作者信息

Jamilah J, Hatta M, Natzir R, Umar F, Sjahril R, Agus R, Junita A R, Dwiyanti R, Primaguna M R, Sabir M

机构信息

Alauddin State Islamic University, Makassar, Indonesia.

Postgraduate Program of Medical Science, Indonesia.

出版信息

New Microbes New Infect. 2020 Oct 17;38:100793. doi: 10.1016/j.nmni.2020.100793. eCollection 2020 Nov.

Abstract

The surveillance of multidrug-resistant (MDR) H58 typhoid is highly important, especially in endemic areas. MDR strain detection is needed by using a simple PCR technique that only uses a pair of primers. This is conducted considering the detection of Typhi strains that have been carried out so far are only using antimicrobial sensitivity tests to determine microbial resistance phenotypically and to determine genotypically using complex molecular techniques. We aimed to analyse the existence of Typhi MDR H58 in patients with typhoid fever in Makassar, Indonesia. A total of 367 blood samples of typhoid fever patients were collected from April 2018 until April 2019. The blood sample was cultured, then confirmed via simple PCR. All of the confirmed samples were tested for susceptibility against antibiotics and molecularly analysed for MDR H58 existence using a simple PCR technique. We found 7% (27/367) of the samples to be positive by both blood culture and PCR. All 27 isolates were found to be sensitive to sulfamethoxazole/trimethoprim. The lowest drug sensitivities were to amoxicillin, at one (3.7%) of 27 isolates, and ampicillin, at 13 (48.1%) of 27 isolates. Typhi H58 PCR results showed that one (3.7%) of 27 isolates carried a positive fragment of 993 bp that led to the H58 strain, since the deletion flanks this fragment. The isolate was also found to be resistant to amoxicillin and fluoroquinolone according to a sensitivity test. Further molecular analysis needs to be conducted to examine the single isolate that carried the 933 bp fragment.

摘要

监测多重耐药(MDR)H58伤寒杆菌非常重要,尤其是在流行地区。需要使用仅一对引物的简单PCR技术来检测MDR菌株。之所以这样做,是因为迄今为止对伤寒杆菌的检测仅采用抗菌药敏试验来从表型上确定微生物耐药性,并采用复杂的分子技术从基因型上进行确定。我们旨在分析印度尼西亚望加锡伤寒热患者中伤寒杆菌MDR H58的存在情况。2018年4月至2019年4月共收集了367份伤寒热患者的血样。对血样进行培养,然后通过简单PCR进行确认。所有确认的样本都进行了抗生素敏感性测试,并使用简单PCR技术对MDR H58的存在进行分子分析。我们发现7%(27/367)的样本血培养和PCR均呈阳性。所有27株分离菌对磺胺甲恶唑/甲氧苄啶敏感。最低药敏率是对阿莫西林,27株分离菌中有1株(3.7%),对氨苄西林,27株分离菌中有13株(48.1%)。伤寒杆菌H58的PCR结果显示,27株分离菌中有1株(3.7%)携带993 bp的阳性片段,该片段导致H58菌株的出现,因为该片段两侧有缺失。根据药敏试验,该分离菌对阿莫西林和氟喹诺酮也耐药。需要进一步进行分子分析以检测携带933 bp片段的单一分离菌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb2f/7695904/1a97f252155a/gr1.jpg

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