Madumali Weerasekara, G. Vidanapathirana, Carmen Li, Asanka Tennegedara, Rasadani Dissanayake, A. Ekanayake, Muditha Abeykoon, M. Kothalawala, V. Liyanapathirana, Margaret Ip
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PCR was used to identify SpeA, SpeB, SpeC, SpeF, SpeG, smez, and ssa as virulence markers. Selected GAS isolates were emm-typed using the updated CDC protocol. All 51 isolates were susceptible to penicillin. The number of isolates non-susceptible to erythromycin was 16. The commonest resistance determinant identified was erm(B) (11/16). Tetracycline non-susceptibility was found in 36 (70.6 %) isolates and 26 of them contained the tet(M) gene. Thirteen (25.5 %) isolates were resistant to both tetracycline and erythromycin, while 12 (23.5 %) isolates were sensitive to both antibiotics. The commonest virulence markers detected among the isolates were SpeB (44, 86.3 %), SpeG (36, 70.6 %), and SpeF (35, 68.6 %), while SpeJ (15, 29.4 %), SpeA (10, 19.6 %), and ssa (5,9.8 %) were less common. The emm types were diverse. In conclusion, the GAS isolates studied showed resistance to erythromycin and tetracycline, while retaining universal susceptibility to penicillin. 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引用次数: 0
摘要
A β溶血性链球菌(GAS)或化脓性链球菌是一种人类病原体,可引起一系列感染,包括咽炎、蜂窝组织炎、脓疱疮、猩红热、中毒性休克综合征和坏死性筋膜炎。本研究描述了从斯里兰卡侵袭性感染中分离出的 51 株 GAS 的特征,重点是耐药性特征、耐药性遗传决定因素和毒力标记。对分离株进行了青霉素、红霉素、克林霉素和四环素敏感性检测。在耐红霉素的分离株中检测到了erm(A)、erm(B)和mef(A),而在耐四环素的分离株中检测到了tet(M)。利用聚合酶链式反应鉴定了作为毒力标记的 SpeA、SpeB、SpeC、SpeF、SpeG、smez 和 ssa。根据最新的疾病预防控制中心(CDC)方案,对选定的 GAS 分离物进行了 emm 分型。所有 51 个分离株都对青霉素敏感。对红霉素不敏感的分离株有 16 个。最常见的耐药基因是erm(B)(11/16)。有 36 个(70.6%)分离物对四环素不敏感,其中 26 个含有 tet(M) 基因。13个分离株(25.5%)对四环素和红霉素均有抗药性,12个分离株(23.5%)对两种抗生素均敏感。分离物中最常见的毒力标记是 SpeB(44 个,86.3%)、SpeG(36 个,70.6%)和 SpeF(35 个,68.6%),而 SpeJ(15 个,29.4%)、SpeA(10 个,19.6%)和 ssa(5 个,9.8%)则不太常见。emm类型多种多样。总之,所研究的 GAS 分离物表现出对红霉素和四环素的抗药性,同时对青霉素保持普遍敏感性。此外,这些分离物的遗传背景各不相同,毒力基因和emm类型也各不相同。
Characterization of group A streptococci causing invasive diseases in Sri Lanka
Group A β haemolytic streptococcus (GAS) or Streptococcus pyogenes is a human pathogen that causes an array of infections, including pharyngitis, cellulitis, impetigo, scarlet fever, toxic shock syndrome, and necrotizing fasciitis. The present study characterizes 51 GAS isolates from invasive infections in Sri Lanka, focusing on resistance profiles, genetic determinants of resistance, and virulence markers. Isolates were tested for sensitivity to penicillin, erythromycin, clindamycin, and tetracycline. The presence of erm(A), erm(B), and mef(A) was detected in erythromycin-resistant isolates, while tet(M) was detected in the tetracycline-resistant isolates. PCR was used to identify SpeA, SpeB, SpeC, SpeF, SpeG, smez, and ssa as virulence markers. Selected GAS isolates were emm-typed using the updated CDC protocol. All 51 isolates were susceptible to penicillin. The number of isolates non-susceptible to erythromycin was 16. The commonest resistance determinant identified was erm(B) (11/16). Tetracycline non-susceptibility was found in 36 (70.6 %) isolates and 26 of them contained the tet(M) gene. Thirteen (25.5 %) isolates were resistant to both tetracycline and erythromycin, while 12 (23.5 %) isolates were sensitive to both antibiotics. The commonest virulence markers detected among the isolates were SpeB (44, 86.3 %), SpeG (36, 70.6 %), and SpeF (35, 68.6 %), while SpeJ (15, 29.4 %), SpeA (10, 19.6 %), and ssa (5,9.8 %) were less common. The emm types were diverse. In conclusion, the GAS isolates studied showed resistance to erythromycin and tetracycline, while retaining universal susceptibility to penicillin. Additionally, these isolates exhibited diverse genetic backgrounds, displaying varying patterns of virulence genes and emm types.