产内酰胺酶的广谱大肠杆菌孕妇及其新生儿的抗生素耐药模式

Carol Suzie Titsamp Lacmago, Simon Ngamli Fewou
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摘要

在世界范围内,健康孕妇携带ctx - m型广谱β -内酰胺酶(ESBL)产生大肠杆菌及其传播给新生儿的发生率正在增加。ESBL-E大肠杆菌,特别是ctx - m型的携带可引起新生儿败血症的早发或晚发,导致发病率和死亡率增加。虽然在一些国家已经报道了产ESBL-E的产妇分娩和母婴传播,但在喀麦隆,产ctx - m型esbl -大肠杆菌在孕妇中的流行及其在新生儿中的传播尚未见报道。我们在这里描述了携带ctx - m型产esbl大肠杆菌孕妇在雅芳德妇产科和儿科医院的新生儿病房及其传播给新生儿。在102例住院孕妇及其新生儿中,直肠定植大肠杆菌分别为88株(86.3%)和75株(73.5%)。母鼠分离的大肠杆菌对β-内酰胺类和磺胺类抗生素耐药率较高,对其他抗生素家族(氨基苷类、喹诺酮类和氟喹诺酮类)耐药率较低。相比之下,只有头孢噻肟(100%)对新生儿大肠杆菌的耐药率更高。这可能表明母亲和新生儿之间存在不同的污染源。孕妇及其新生儿携带ctx - m型产esbl大肠杆菌的比例分别为30.7%和14.7%。这表明,除了母亲,新生儿还有其他的殖民化来源。事实上,多元回归分析表明,新生儿暴露于母亲和医院环境(例如医院环境)中产生ctx - m型esbl的大肠杆菌。照顾者)。总的来说,目前的研究可能为建立有效的治疗策略提供见解,以对抗产生ctx - m型esbl的大肠杆菌的母婴传播和医院传播。
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Antibiotic resistance pattern of extended-spectrum-beta lactamases-producing Escherichia coli isolated from pregnant women and their new born
The incidence of healthy pregnant women carrying CTX-M-type extended-spectrum beta-lactamase (ESBL)-producing E. coli and their transmission to neonates is increasing worldwide. ESBL-E coli and especially the carriage of CTX-M-type causes early or late onset of neonatal sepsis, resulting in increased morbidity and mortality rates. Although maternal carriage and maternal-neonatal transmissions of ESBL-E have been reported in several countries, the prevalence of CTX-M-type ESBL-producing E. coli in pregnant women and its transmission to newborns at birth in Cameroon has not been reported yet. We describe here the carriage of CTX-M-type ESBL-producing E. coli pregnant women in neonatal ward of the Yaoundé gyneco-obstetric and pediatric hospital and their transmission to newborns. Among the 102 pregnant women and their newborns present in the ward, 88 (86.3%) and 75 (73.5%) E. coli strains were detected in rectal colonization, respectively. Antibiotic susceptibility testing of E. coli isolated from the mothers indicated a higher resistance rate to antibiotics of the β-lactams and sulfamide families, while the resistances to other antibiotic families (aminosides, quinolones and fluoroquinolones) were low. Comparatively, only cefotaxime (100%) showed a higher resistance rate to E. coli isolated from newborns. This may suggest a different source of contamination between mothers and newborns. Moreover, the rate of carriage of CTX-M-type ESBL-producing E. coli in pregnant mother and their newborns were 30.7 % and 14.7 %, respectively. This suggests that newborns had other colonization sources than the mothers. Indeed, multiple regression analysis indicated that newborns were exposed to CTX-M-type ESBL-producing E. coli from mothers and that from the hospital environment (eg. caregivers). Overall, the current investigation may provide insight on establishing an efficient therapeutic strategy against materno-neonatal and nosocomial transmission of CTX-M-type ESBL-producing E. coli.
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