Gabor Caitlin E, Chong Charlotte E, Lemme-Dumit Jose M, Hazen Tracy H, Baker Kate S, Kotloff Karen L, Kasumba Irene N, Tennant Sharon M, Badji Henry, Hossain M Jahangir, Omore Richard, Ochieng Benjamin, Awuor Alex O, Ogwel Billy, Juma Jane, Barry Eileen M, Rasko David A
Institute for Genome Sciences, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
mBio. 2025 Jan 8;16(1):e0221024. doi: 10.1128/mbio.02210-24. Epub 2024 Dec 10.
serotype 6 (6) is one of the most common serotypes recovered from surveillance studies of moderate to severe diarrhea. Despite the clinical significance of 6, this serotype is understudied. In this work, we have performed both serotype-specific genomic and phenotypic comparisons of 6 isolates to one another and non-. serotypes. Comparative genomic analyses identified significant nucleotide homology between 6 strains ( = 325), despite a broad range of collection timeframes and geographic locations. We identified 6 specific factors, including a potential novel virulence factor (type II secretion system). Additionally, we identified established virulence genes () and metabolic genes () that were absent in 6 strains while present in the majority of 728 non-6 strains. Complete sequencing of 11 clinical 6 strains, demonstrated that the 6 virulence plasmid (pINV) is 38 kb smaller than the average non-6 pINV (228 kb). Comparisons of species level antibiotic susceptibility highlighted that clinical 6 isolates from Africa in the Global Enteric Multicenter Study (GEMS) and Vaccine Impact on Diarrhea in Africa (VIDA) study demonstrated geographic, serotype-specific susceptibility pattern. Phenotypic analyses of 6 identified reduced intracellular invasion and cytokine induction from HT-29 cells, as well as reduced Ipa protein effector secretion, compared with serotype 2a strain 2457T. Together these data highlight conserved and unique serotype-specific genotypic and phenotypic features for 6. This level of conservation has not been noted for other serotypes and is promising for vaccine and diagnostic assays to provide global 6-specific coverage.IMPORTANCEShigellosis is an ongoing global public health crisis with >270 million annual episodes among all age groups; however, the greatest disease burden is among children in low- and middle-income countries (LMIC). The lack of a licensed vaccine and the observed rise in antimicrobial-resistant spp. highlights the urgency for effective preventative and interventional strategies. The inclusion of serotype 6 (6) is a necessary component of a multivalent vaccine strategies based on its clinical and epidemiological importance. Given the genomic diversity of 6 compared with other serotypes and 6 unique O-antigen core structure, serotype-specific characterization of 6 is a critical step to inform -directed vaccine and alternative therapeutic designs. Herein, we identified conserved genomic content among a large collection of temporally and geographically diverse 6 clinical isolates and characterized genotypic and phenotypic properties that separate 6 from non-6 serotypes.
血清型6(6型)是从中度至重度腹泻监测研究中分离出的最常见血清型之一。尽管6型具有临床意义,但对该血清型的研究仍不充分。在这项研究中,我们对6型分离株之间以及与非6型血清型进行了血清型特异性的基因组和表型比较。比较基因组分析确定了6型菌株之间存在显著的核苷酸同源性(= 325),尽管它们的采集时间范围和地理位置广泛。我们鉴定出6个特异性因子,包括一种潜在的新型毒力因子(II型分泌系统)。此外,我们还鉴定出在6型菌株中不存在而在728株非6型菌株中的大多数中存在的已确定的毒力基因()和代谢基因()。对11株临床6型菌株进行全测序表明,6型毒力质粒(pINV)比非6型平均pINV(约228 kb)小约38 kb。全球肠道多中心研究(GEMS)和非洲腹泻疫苗影响研究(VIDA)中来自非洲的临床6型分离株的种水平抗生素敏感性比较突出表明,其呈现出地理和血清型特异性的敏感性模式。与2a血清型菌株2457T相比,对6型进行的表型分析确定其对HT - 29细胞的细胞内侵袭和细胞因子诱导减少,以及Ipa蛋白效应物分泌减少。这些数据共同突出了6型保守且独特的血清型特异性基因型和表型特征。其他血清型尚未发现这种程度的保守性,这对于提供全球6型特异性覆盖的疫苗和诊断检测来说很有前景。
重要性
志贺菌病是一场持续的全球公共卫生危机,所有年龄组每年发病超过2.7亿例;然而,最大的疾病负担集中在低收入和中等收入国家(LMIC)的儿童中。缺乏许可的志贺菌疫苗以及观察到的抗菌药物耐药志贺菌属物种的增加凸显了有效预防和干预策略的紧迫性。鉴于6型血清型(6)的临床和流行病学重要性,将其纳入多价疫苗策略是必要的组成部分。鉴于6型与其他志贺菌血清型相比具有基因组多样性以及6型独特的O抗原核心结构,对6型进行血清型特异性表征是指导志贺菌定向疫苗和替代治疗设计的关键步骤。在此,我们在大量时间和地理上不同的6型临床分离株中鉴定出保守的基因组内容,并表征了将6型与非6型志贺菌血清型区分开来的基因型和表型特性。