Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Department of Genetics, Research Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
J Matern Fetal Neonatal Med. 2023 Dec;36(1):2207113. doi: 10.1080/14767058.2023.2207113.
Respiratory distress is common in neonates admitted to neonatal intensive care units. Additionally, infectious diseases such as intrauterine infections or vertical transmission are important underlying causes of respiratory failure. However, pathogens often cannot be identified in neonates, and there are many cases in which antibacterial drugs are empirically administered. Next-generation sequencing (NGS) is advantageous in that it can detect trace amounts of bacteria that cannot be detected by culturing or bacteria that are difficult to cultivate. However, there are few reports on the diagnosis of infectious diseases using NGS in the neonatal field, especially those targeting respiratory distress.
The purpose of our study was to investigate the microorganisms associated with neonatal respiratory distress and to determine whether less invasive collection specimens such as plasma and gastric fluid are useful.
Neonates were prospectively recruited between January and August 2020 from Nagoya University Hospital. The inclusion criteria were as follows: 1) admission to the neonatal intensive care unit; 2) respiratory distress presentation within 48 h of birth; and 3) suspected infection, collection of blood culture, and administration of antibiotics. Plasma samples and blood cultures were simultaneously collected. Gastric fluid samples were also collected if the patient was not started on enteral nutrition. Information on the patients and their mothers were collected from the medical records. DNA was extracted from 140 µL of plasma and gastric fluid samples. DNA sequencing libraries were prepared, and their quality was analyzed. DNA libraries were sequenced using high-throughput NGS. The NGS data of plasma and gastric fluid samples were analyzed using the metagenomic pipeline PATHDET, which calculated the number of reads assigned to microorganisms and their relative abundance. Putative pathogens were listed.
Overall, 30 plasma samples and 25 gastric fluid samples from 30 neonates were analyzed. Microorganism-derived reads of gastric fluid samples were significantly higher than those of plasma samples. Transient tachypnea of the newborn was the most common cause of respiratory distress with 13 cases (43%), followed by respiratory distress syndrome with 7 cases (23%). There were 8 cases (29%) of chorioamnionitis and 7 cases (25%) of funisitis pathologically diagnosed. All blood cultures were negative, and only two gastric fluid cultures were positive for group B (Patient 15) and (Patient 24). Putative pathogens that met the positive criteria for PATHET were detected in four gastric fluid samples, one of which was group B from Patient 15. In the gastric fluid sample of Patient 24, were detected by NGS but did not meet the positive criteria for PATHDET. Cluster analysis of the plasma samples divided them into two study groups, and the indicator genera of each cluster ( or ) are shown in Figure 1. Clinical findings did not show any significant differences between the two groups. Cluster analysis of the gastric fluid samples divided them into three study groups, and the indicator genera of each cluster (, , and ) are shown in Figure 2. The incidence rate of chorioamnionitis was significantly higher in group than in the other two groups.
Gastric fluid may be useful for assessing neonatal patients with respiratory distress. To the best of our knowledge, this was the first study to reveal that the presence of in the gastric fluid of neonates with respiratory distress was associated with chorioamnionitis. The early diagnosis of intra-amniotic infections using gastric fluid and its treatment may change the treatment strategy for neonatal respiratory distress. Screening for in neonates with respiratory distress may reduce the need for empirical antibiotic administration. Further research is required to confirm these findings.
呼吸窘迫在新生儿重症监护病房收治的新生儿中很常见。此外,宫内感染或垂直传播等传染病也是呼吸衰竭的重要潜在原因。然而,新生儿的病原体通常无法确定,并且有许多情况下需要经验性地使用抗菌药物。下一代测序(NGS)的优势在于它可以检测到培养或难以培养的细菌的痕量。然而,在新生儿领域使用 NGS 诊断传染病的报道很少,特别是针对呼吸窘迫的报道。
我们的研究目的是调查与新生儿呼吸窘迫相关的微生物,并确定是否可以使用侵入性较小的采集标本,如血浆和胃液。
2020 年 1 月至 8 月期间,名古屋大学医院前瞻性招募了新生儿。纳入标准如下:1)入住新生儿重症监护病房;2)出生后 48 小时内出现呼吸窘迫;3)疑似感染,采集血培养和使用抗生素。同时采集血浆样本和血培养。如果患者未开始肠内营养,则采集胃液样本。从病历中收集患者及其母亲的信息。从 30 名新生儿的 30 个血浆样本和 25 个胃液样本中提取 140 μL 的 DNA。制备 DNA 测序文库,并分析其质量。使用高通量 NGS 对 DNA 文库进行测序。使用宏基因组分析管道 PATHDET 分析血浆和胃液样本的 NGS 数据,该管道计算分配给微生物的读数及其相对丰度。列出潜在病原体。
总体而言,分析了 30 名新生儿的 30 个血浆样本和 25 个胃液样本。胃液样本中微生物衍生的读数明显高于血浆样本。新生儿暂时性呼吸急促是呼吸窘迫最常见的原因,有 13 例(43%),其次是呼吸窘迫综合征,有 7 例(23%)。有 8 例(29%)的绒毛膜炎和 7 例(25%)的脐带炎经病理诊断。所有血培养均为阴性,仅 2 例胃液培养阳性,分别为患者 15 的 B 群 和患者 24 的 。在 4 个胃液样本中检测到符合 PATHET 阳性标准的潜在病原体,其中一个来自患者 15 的 B 群 。在患者 24 的胃液样本中,通过 NGS 检测到 ,但不符合 PATHDET 的阳性标准。对血浆样本的聚类分析将它们分为两组,每个聚类的指示菌(或 )如图 1 所示。两组之间的临床发现没有明显差异。对胃液样本的聚类分析将它们分为三组,每个聚类的指示菌(、和 )如图 2 所示。组 中的绒毛膜炎发生率明显高于其他两组。
胃液可能有助于评估患有呼吸窘迫的新生儿患者。据我们所知,这是第一项表明新生儿呼吸窘迫患者胃液中存在 的研究与绒毛膜炎有关。使用胃液早期诊断羊膜内感染并进行治疗可能会改变新生儿呼吸窘迫的治疗策略。对呼吸窘迫的新生儿进行 筛查可能会减少经验性使用抗生素的需求。需要进一步研究来证实这些发现。