Microbiologic clearance in macrolide-resistant Bordetella pertussis: An infant treated with sulfamethoxazole-trimethoprim — A case timeline

IF 1.7 4区 医学 Q3 INFECTIOUS DISEASES
Journal of Infection and Chemotherapy Pub Date : 2026-02-01 Epub Date: 2026-01-09 DOI:10.1016/j.jiac.2026.102907
Yu Kuramochi , Meiwa Shibata , Mikako Morinaga , Tomoyuki Tame , Kazue Kinoshita , Osamu Saito , Yuho Horikoshi
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引用次数: 0

Abstract

Amid a large-scale resurgence of pertussis in Japan in 2025, concern is growing about the spread of macrolide-resistant Bordetella pertussis (MRBP)—prevalent in China—posing a clinical challenge, particularly in infants. We describe a term 6-week-old unvaccinated infant with life-threatening MRBP. Diagnosis was confirmed by culture and multiplex PCR. The isolate harbored the 23S rRNA A2047G mutation. Daily microbiology (Gram stain, culture, quantitative PCR) was performed on nasopharyngeal swabs and lower-airway aspirates. The infant received empiric azithromycin and a 14-day course of sulfamethoxazole–trimethoprim (SMX-TMP) and recovered without sequelae. Nasopharyngeal cultures became negative by Day 2 of SMX-TMP therapy, and lower-airway aspirate cultures by Day 3. Nasopharyngeal quantitative PCR was below the detection limit by Day 7. Lower-airway quantitative PCR declined through Day 7, and sampling ceased after extubation. These observations suggest that bacteriologic clearance with SMX-TMP may occur on a time frame similar to that used to discontinue precautions for macrolide-susceptible disease, commonly five days after starting effective therapy. During the current resurgence in Japan, transmission appears concentrated among school-aged children, whereas the national vaccination program targets only those under two years of age. Introducing booster doses at 5–6 and 11–12 years may help reduce school-based transmission. In addition, maternal booster vaccination during pregnancy could protect young infants through the transplacental transfer of maternal pertussis antibodies.
大环内酯耐药百日咳博德氏菌的微生物清除率:用磺胺甲恶唑-甲氧苄啶治疗的婴儿-一个病例时间表。
2025年,百日咳将在日本大规模复发,人们越来越担心大环内酯耐药百日咳(MRBP)的传播,这在中国流行,对临床,特别是婴儿构成挑战。我们描述了一个6周大的婴儿未接种疫苗危及生命的MRBP。经培养和多重PCR确诊。该分离物携带23S rRNA A2047G突变。每日对鼻咽拭子和下气道吸入物进行微生物学(革兰氏染色、培养、定量PCR)检测。婴儿接受经验阿奇霉素治疗和14天的磺胺甲恶唑-甲氧苄啶疗程(SMX-TMP),痊愈无后遗症。SMX-TMP治疗第2天鼻咽培养呈阴性,第3天下气道培养呈阴性。第7天,鼻咽定量PCR低于检测限。下气道定量PCR在第7天下降,拔管后停止采样。这些观察结果表明,SMX-TMP的细菌学清除可能发生在与大环内酯易感疾病停止预防措施相似的时间框架内,通常在开始有效治疗后5天。在日本目前的死灰复燃期间,传播似乎集中在学龄儿童中,而国家疫苗接种计划仅针对两岁以下儿童。在5-6岁和11-12岁时引入加强剂可能有助于减少学校传播。此外,怀孕期间母亲加强接种疫苗可以通过经胎盘转移母亲百日咳抗体来保护婴儿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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