Department of Clinical Investigations, Brooke Army Medical Center, San Antonio, TX, USA.
Department of Pathology and Area Laboratory Services, Brooke Army Medical Center, San Antonio, TX, USA.
Ann Clin Microbiol Antimicrob. 2020 Nov 26;19(1):55. doi: 10.1186/s12941-020-00396-6.
Group B Streptococcus (GBS) infections caused by Streptococcus agalactiae is a leading cause of meningitis and sepsis in neonates, with early-onset GBS symptoms emerging during the first week of life and late-onset occurring thereafter. Perinatal transmission of GBS to the neonate through the birth canal is the main factor associated with early-onset neonate infections, while less is understood about the source of late-onset infections.
In this report we describe a case of twin ex-premature infants who presented one month after birth with GBS septicemia. The mother had been appropriately screened at gestational age 35-37 weeks and laboratory methods failed to detect GBS colonization by culture or clinical molecular methods. In attempts to identify and isolate the source of GBS infection, additional surveillance swabs were collected from the mother at the time of neonate admission. Culture and a commercially available, FDA-cleared molecular PCR assay were performed.
No GBS was detected from swabs collected from the perianal, thigh/groin or axillary areas. However, expressed breast milk and swabs from the breastmilk pump were positive by both methods. Since simultaneous culture and molecular methods which used breastmilk as a source were performed, investigators ascertained the limit of detection for GBS in breastmilk. The limit of detection was determined to be tenfold lower than that of LIM-broth enriched cultures-the FDA-approved source. Subsequent whole genome sequencing (WGS) analysis of isolates recovered from breastmilk and blood cultures from the infants demonstrated all strains were related and characterized as ST-452. Both infants responded very well to treatment and continued to have no related events or concerns at the two-year follow up appointment.
Strain type 452 (capsular type IV) has recently emerged as a hypervirulent strain and has previously been documented as causing GBS infections in elderly populations. Antibiotic therapy resolved both mother and infant infections. Subsequent testing for the presence of GBS in breastmilk samples also showed an absence of bacteria. This is the first report of infant twins late-onset GBS infections caused by the hypervirulent S. agalactiae ST-452 with breastmilk as the source.
由无乳链球菌引起的 B 群链球菌(GBS)感染是导致新生儿脑膜炎和败血症的主要原因,早发型 GBS 症状在生命的第一周出现,而晚发型则在此之后出现。通过产道将 GBS 传递给新生儿是导致早发型新生儿感染的主要因素,而对于晚发型感染的来源则知之甚少。
在本报告中,我们描述了一对双胞胎早产儿的病例,他们在出生后一个月出现 GBS 败血症。母亲在妊娠 35-37 周时已进行了适当的筛查,且实验室方法未能通过培养或临床分子方法检测到 GBS 定植。为了确定并分离 GBS 感染源,在新生儿入院时从母亲身上采集了额外的监测拭子。进行了培养和一种市售的、经美国食品和药物管理局批准的分子 PCR 检测。
从肛周、大腿/腹股沟或腋窝区域采集的拭子均未检测到 GBS。然而,两种方法均从母乳和母乳泵拭子中检测到 GBS 阳性。由于同时进行了使用母乳作为来源的培养和分子方法,研究人员确定了母乳中 GBS 的检测限。检测限比 LIM-肉汤富集培养物(美国食品和药物管理局批准的来源)低十倍。随后对从婴儿母乳和血液培养物中分离出的分离株进行全基因组测序(WGS)分析表明,所有菌株均相关,且均为 ST-452 型。两名婴儿对治疗反应良好,在两年的随访时继续没有相关事件或担忧。
452 型(荚膜类型 IV)菌株最近已成为一种高毒力菌株,并且以前曾被记录为导致老年人群 GBS 感染的原因。抗生素治疗解决了母亲和婴儿的感染。随后对母乳样本中是否存在 GBS 的检测也显示没有细菌。这是首例由高毒力无乳链球菌 ST-452 引起的婴儿双胞胎晚发型 GBS 感染的报告,感染源为母乳。