Department of Plant and Microbial Biology, North Carolina State University, Raleigh, North Carolina, USA.
Centers for Disease Control and Prevention (CDC), EDLB/DFWED, Atlanta, Georgia, USA.
Microbiol Spectr. 2023 Feb 14;11(1):e0274522. doi: 10.1128/spectrum.02745-22. Epub 2022 Dec 6.
Listeria monocytogenes is a Gram-positive, facultative intracellular foodborne pathogen capable of causing severe, invasive illness (listeriosis). Three serotypes, 1/2a, 1/2b, and 4b, are leading contributors to human listeriosis, with 4b including the major hypervirulent clones. The multiplex PCR scheme developed by Doumith and collaborators employs primers targeting specific lineages (e.g., lineage II-specific , lineage I-specific ) or serotypes (e.g., serotype 4b-specific ). The Doumith scheme (DS) is extensively employed for molecular serotyping of L. monocytogenes due to its high accuracy, relative ease, and affordability. However, for certain strains, the DS serotype designations are in conflict with those relying on antibody-based schemes or whole-genome sequence (WGS) analysis. In the current study, all 27 tested serotype 4b strains with sequence type 782 (ST782) within the hypervirulent clonal complex 2 (CC2) were designated 1/2b/3b using the DS. These strains lacked the serotype 4b-specific gene , while retaining , which, together with , yields the DS 1/2b/3b profile. Furthermore, 15 serotype 1/2a strains of four STs, mostly from water, were designated 1/2b/3b using the DS. These strains lacked the cassette but harbored genomic islands with , thus yielding the DS 1/2b/3b profile. Lastly, we investigated a novel, dual 1/2a-1/2b profile obtained using the DS with 21 serotype 1/2a strains of four STs harboring both the cassette and genomic islands with . The findings suggest that for certain strains and clones of L. monocytogenes the DS designations should be viewed with caution and complemented with alternative tools, e.g., traditional serotyping or WGS analysis. Listeria monocytogenes is a foodborne pathogen responsible for severe illness (listeriosis), especially in pregnant women and their fetuses, immunocompromised individuals, and the elderly. Three serotypes, 1/2a, 1/2b, and 4b, account for most human listeriosis, with certain serotype 4b clonal complexes (CCs) overrepresented in human disease. Serotyping remains extensively employed in epidemiologic investigations, and a multiplex PCR-based serotyping scheme is widely used. However, the PCR gene targets can be lost or gained via horizontal gene transfer, leading to novel PCR profiles without known serotype designations or to incorrect serotype assignments. Thus, an entire serotype 4b clone of the hypervirulent CC2 would be misidentified as serotype 1/2b, and several strains of serotype 1/2a would be identified as serotype 1/2b. Such challenges are especially common in novel clones from underexplored habitats, e.g., wildlife and surface water. The findings suggest caution in application of molecular serotyping, while highlighting 's diversity and potential for horizontal gene transfer.
李斯特菌是一种革兰氏阳性、兼性细胞内食源性病原体,能够引起严重的侵袭性疾病(李斯特菌病)。三种血清型,1/2a、1/2b 和 4b,是导致人类李斯特菌病的主要原因,其中 4b 包括主要的高毒力克隆。Doumith 及其同事开发的多重 PCR 方案采用针对特定谱系(例如谱系 II 特异性、谱系 I 特异性)或血清型(例如血清型 4b 特异性)的引物。由于其准确性高、相对容易和价格合理,Doumith 方案(DS)被广泛用于李斯特菌的分子血清分型。然而,对于某些菌株,DS 血清型的命名与基于抗体的方案或全基因组序列(WGS)分析不一致。在本研究中,所有 27 株经测试的血清型 4b 菌株,序列类型为 782(ST782),均属于高毒力克隆复合体 2(CC2),使用 DS 被指定为 1/2b/3b。这些菌株缺乏血清型 4b 特异性基因,而保留了 ,与一起,产生了 DS 1/2b/3b 图谱。此外,DS 还将四个 ST 的 15 株血清型 1/2a 菌株指定为 1/2b/3b,这些菌株缺乏 基因盒,但携带基因组岛,其中包含 ,因此产生了 DS 1/2b/3b 图谱。最后,我们研究了使用 DS 获得的一种新型双重 1/2a-1/2b 图谱,该图谱来自四个 ST 的 21 株血清型 1/2a 菌株,这些菌株既携带 基因盒,又携带基因组岛。研究结果表明,对于某些李斯特菌菌株和克隆,DS 命名应谨慎使用,并辅以替代工具,例如传统血清分型或 WGS 分析。李斯特菌是一种食源性病原体,可导致严重疾病(李斯特菌病),特别是在孕妇及其胎儿、免疫功能低下者和老年人中。三种血清型,1/2a、1/2b 和 4b,占人类李斯特菌病的大多数,某些血清型 4b 克隆复合体(CC)在人类疾病中过度表达。血清分型在流行病学研究中仍广泛应用,基于多重 PCR 的血清分型方案也广泛应用。然而,PCR 基因靶标可通过水平基因转移丢失或获得,导致新型 PCR 图谱没有已知的血清型命名或错误的血清型分配。因此,整个高毒力 CC2 的血清型 4b 克隆将被错误地鉴定为血清型 1/2b,而几株血清型 1/2a 菌株将被鉴定为血清型 1/2b。这种挑战在尚未充分探索的栖息地(例如野生动物和地表水)中的新型克隆中尤为常见。研究结果表明,在应用分子血清分型时应谨慎,同时强调李斯特菌的多样性和水平基因转移的潜力。