Background
Group B
streptococcus (GBS), also referred to as
Streptococcus agalactiae, is the sole member of the Lancefield group and a major cause of invasive infections in infants, especially those living in China, due to the lack of routine screening for GBS maternal colonization and intrapartum antibiotic prophylaxis (IAP) implementation. GBS is one of the main pathogens responsible for morbidity and mortality among infants in many countries, including China [
1,
2]. The incidence of invasive GBS infection among newborns and infants varies greatly around the world, from 0.57/1000 live births in Europe to 1.21/1000 live births in Africa [
3]. There is a paucity of data on the prevalence of invasive GBS infections in infants in China. Further, there are speculations that China may loosen the current two-child limit; thus, leading to the birth of more infants every year. Hence, it is very important to reduce the rate of these infections among infants in China.
The distribution of serotypes is closely related to the epidemiology of GBS infections. On the basis of the composition of capsular polysaccharide (CPS), the following ten serotypes are currently recognized: Ia, Ib, and II-IX [
4,
5]. The prevalence of different serotypes varies according to the time and geographic origin. Five studies in middle-income countries showed that serotype III accounted for nearly half of the isolates, followed by serotypes Ia, II, and V [
3]. The most prevalent serotypes (Ia, Ib, II, III, and V) have been reported to account for over 96% of serotypes in the United States, 93% in Europe, and 89% in the Western Pacific [
6]. However, the distribution of GBS serotypes in Asia has been sparsely surveyed.
In young infants, invasive GBS infections are usually categorized into early-onset disease (EOD, occurring at the age of 0–6 days) and late-onset disease (LOD, occurring at the age of 7–89 days).
In the United States, IAP has decreased the incidence of GBS-EOD from 1.7 cases per 1000 live births in 1993 to 0.4 cases per 1000 live births in 2008 [
7]. However, IAP cannot prevent GBS-LOD [
8]. In addition, widespread IAP can cause anaphylaxis or lead to the development of antibiotic-resistant strains. An epidemiological study showed that the distribution of serotypes in a pathogen is an important precondition for formulating serotype-based vaccines [
9]. A safe and efficacious vaccine against the most common serotypes can prevent most infant GBS infections (early and late onset infections).
Thus, our study is aimed at providing new information on GBS serotypes and the associated clinical features of invasive GBS isolates in a Chinese population and obtaining reference values for developing methods to prevent GBS infections.
Methods
Subject population
Seven hospitals reported 95,941 live births and an incidence of invasive GBS disease of 0.88 cases/1000 live births during the study period. Eighty-four GBS strains were obtained from the Women and Children’s Hospital of Xiamen University (Xiamen, China), The First Affiliated Hospital of Xiamen University (Xiamen, China), Zhangzhou Affiliated Hospital of Fujian Medical University (Zhangzhou, China), Longyan First Affiliated Hospital of Fujian Medical University (Longyan, China), Quanzhou Women and Children’s Hospital (Quanzhou, China), Longhai First Affiliated Hospital (Longhai, China), and Zhangzhou Zhengxing Hospital (Zhangzhou, China). Invasive GBS strains were collected prospectively from normally sterile sites (tracheal secretions, gastric fluid, blood, and cerebrospinal fluid). The detection of GBS strains was performed at the bacteriological laboratory of the Women and Children’s Hospital of Xiamen University between June 1, 2016 and June 1, 2018. GBS strains obtained from patients younger than 90 days and the medical records of these patients were retrospectively reviewed. A questionnaire was designed to collect clinical information, including age, symptoms, laboratory data, antibiotic usage, complications, length of hospital stay, gestational age, birth weight, and maternal history. The study protocol was in strict accordance with the ethical standards of the respective regional committee on human experimentation and the Helsinki Declaration of 1975 (revised in 1983). The ethics committee of Xiamen Maternal and Child Care Hospital of human body research approved the study (approval no. KY-2019-033), and the parents of all study participants provided written informed consent.
Definitions
Invasive GBS disease was defined as the isolation of GBS from a normally sterile site using conventional microbiological methods along with signs of clinical disease, such as sepsis, pneumonia, or meningitis [
10] GBS-EOD was defined as invasive GBS disease in newborns 0–6 days of age, and GBS-LOD was defined as invasive GBS disease in infants 7–89 days of age [
10].
Serotyping
Bacteria were cultured in sheep blood agar plates and confirmed using the Christie, Atkins, and Munch Petersen (CAMP) test and a commercially available Streptococcal Grouping Kit according to the methods described in a previous paper [
11]. After culture, all 84 strains were confirmed to be GBS and the isolates were serotyped using a latex agglutination kit (reagents Ia, Ib, and II–IX; Statens Serum Institut, Copenhagen, Denmark) [
12].
Multi-locus sequence typing (MLST)
Chromosomal DNA was extracted from overnight cultures of isolates cultivated at 35 °C on 5% Müeller-Hinton agar using a DNA Mini Kit (QIAGEN, Germany) according to the manufacturer’s instructions. Seven housekeeping genes (
adhP,
pheS,
atr,
glnA,
sdhA,
glcK, and
tkt) were amplified with PCR using oligonucleotide primers [
11]. The amplification products were sequenced by Shenzhen Huada Gene Technology Co. Ltd. The amplification and sequencing primers were submitted to the GBS MLST database (
http://pubmlst.org/sagalactiae/info/primers.shtml) for the purpose of designation. We used the Chromas Lite software (version 2.6.5, Technelysium Pty. Ltd., Tewantin, Queensland, Australia) for correction and the MLST database (
http://pubmlst.org/sagalactiae) to assign alleles at the seven loci. We defined each isolate by the sequence type (ST) [
13].
Statistical analysis
SPSS Statistics for Windows, Version 25.0 (IBM Corp., Armonk, NY, USA) was used to perform statistical analysis. The data for age and the length of hospital stay are presented as medians and interquartile ranges. Qualitative variables were compared using the Chi-square or Fisher’s Exact test. Numerical variables were compared using analysis of variance or non-parametric tests (Kruskal-Wallis H test). The Kaplan-Meier method was used for the analysis of survival time. A log-rank test was used to compare the survival curves among various serotypes. Differences were deemed statistically significant at P < 0.05.
Discussion
There is a paucity of generalizable data on invasive GBS infections among infants in Asia. Additionally, there is a lack of data on the prevalence of invasive GBS infections among infants in China. Thus, we performed this study to assess serotype distribution and to obtain clinical and molecular microbiological information on invasive GBS disease among infants in southern mainland China that will help develop methods to prevent infant GBS infections.
In this study, we observed that GBS infections among infants were most frequently caused by serotype III (60.71%), followed by Ia (16.67%) and Ib (14.29%). The distribution of serotypes of GBS isolates in our study was similar to that reported for Beijing in 2012–2013 by Wang et al., which was as follows: III, 32.1%; Ia, 17.9%; and Ib, 16.1% [
11]. The serotype distribution was also similar to that reported by Lo C-W et al. in Taiwan in 1998–2014, where serotype III caused 53.9% of infection episodes, followed by Ia with 17.0% and Ib with 10.4% [
14]. A recent global review of 6500 invasive GBS isolates from infants showed that serotype III (61.5%) was predominant and 97% of cases were caused by serotypes Ia, Ib, II, III, and V [
11], consistent with a previous study [
15].
After presenting the serotype distribution according to the disease onset, we identified the predominance of serotype III in all age groups. Serotype Ia was the second most prevalent in early onset-GBS, whereas serotype Ib was the second most prevalent in late onset-GBS. Lo C-W et al. reported that serotype III induced approximately half of the infections, but serotype Ia was predominant in patients younger than 72 h [
14]. A worldwide study revealed that serotype III caused nearly half (47%) of GBS-EOD cases and 73.0% of GBS-LOD cases [
10]. Serotypes Ia, Ib, and V were frequently isolated from GBS-EOD (22.8, 8.0, and 10.6%, respectively) and GBS-LOD patients (14.2, 5.3, and 4.0%) [
10]. Data from another global systematic review and meta-analysis [
3] showed that 221 (37%) of 604 early-onset serotypes were type III compared with 347 (53%) of 653 late-onset serotypes and that 242 (40%) early-onset serotypes were type I in contrast with 196 (30%) late-onset serotypes. Thus, it was observed that disease-causing GBS serotypes in infants were similar in terms of prevalence across various regions, with some minimal variations depending on the geographic location, climate, and source of the bacterial isolates. However, there are only a few studies of GBS serotypes in Asia. Our study provides new data on the serotypes of invasive GBS isolates in a Chinese population.
We focused on differential demographics and the clinical presentations of the three most prevalent serotypes, Ia, Ib, and III. Although serotype III was more common, serotype Ia caused significantly higher rates of intrapartum temperature ≥ 37.5 °C, chorioamnionitis, and mortality. A Kaplan-Meier plot from this study revealed that patients with serotype III infections had a higher probability of survival than those with non-serotype III infections including serotype Ia infections, which was consistent with a previous study [
14]. Apart from the lower age of patients with serotype Ia disease, hyper-virulence was considered to be more related to serotype Ia than to serotypes Ib and III. More research should be performed before we can understand the definite reasons for these findings. Basically, serotype III has high invasive potential and is the leader in causing invasive disease worldwide [
3].
This study showed that respiratory distress occurred more frequently in patients with serotype Ia and Ib disease, whereas purulent meningitis was more related to serotype III. It has previously been reported that 86.2% of meningitis cases and 60.8% of sepsis cases were caused by serotype III GBS isolates in European countries and the United States [
16]. Our data also demonstrated that meningitis was dominant in LOD cases compared to EOD cases, and that serotype III was the most prevalent serotype that induced meningitis in LOD cases, in agreement with a previous study [
17]. Thus, serotype III GBS isolates were closely associated with purulent meningitis and serotype Ia tended to associate with pneumonia. This finding is probably due to the different virulence of GBS isolates with various serotypes [
18]. The data revealed an increase in the number of cases of LOD meningitis caused by serotype III, consistent with a previous study [
19]. Moreover, IAP generally has no effect on the incidence of LOD, and GBS can cause diseases in young infants older than three months [
20].
There is limited data concerning MLST for GBS isolates from China. Our research assessed this aspect, and the results showed that ST17 was the most prevalent type (42.86%) among the 84 GBS strains, followed by ST23 (13.10%) and ST19 (10.71%). ST17 was the most common type (68.63%) in serotype III isolates. ST23 was detected specifically in serotype Ia. The percentage of ST17 in the LOD group was significantly higher than that in the EOD group. ST17 and ST19 were found almost exclusively in serotype III, which was in accordance with another study [
21]. In the data from Taiwan, ST23 and ST24 comprised 85% of serotype Ia [
14]. The ST17 clone, which mainly belonged to serotype III, was considered to be hypervirulent and related to meningitis [
14]. This explains why ST17 was more frequently found in LOD in our study. Invasive GBS disease in infants is especially correlated with serotypes III (represented mainly by ST19 in Asia and ST17 in Europe) and Ia (represented mainly by ST23 and ST24) [
22,
23].
GBS disease is not well recognized or reported in China. However, many reports from China show that GBS is a major infectious cause of morbidity and mortality among infants in Chinese population [
24,
25]. In addition, China plans to relax the current two-child limit, which will allow married couples to have more than two children. This relaxation of the policy will result in the birth of more children every year. Thus, to reduce mortality, universal screening for maternal GBS colonization and subsequent IAP should be performed in China. We suggest that a safe and efficacious maternal vaccine against the most common serotypes should be developed and applied because LOD cannot be prevented by IAP [
26]. The serotyping results and ST distribution in our study are important for selecting future GBS vaccines in China.
Our study has some limitations. These include the retrospective nature of the study, low number of GBS isolates obtained, and lack of data from northern China, which may have led to bias in the results.
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