Shuoyue Wang , Xinchun Li , Chenxu Zheng , Juan J. Quereda , Jie Sun , Huochun Yao , Zongfu Wu
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Antibiotic resistance gene analysis identified 21 distinct genes, including the first identification of <em>mef(A)</em>, <em>msr(D)</em>, <em>optrA</em>, <em>lnu(G)</em>, <em>spw</em>, <em>dfrF</em>, and <em>fexA</em> in <em>S. pasteurianus</em>. Strain WUSP082 carried 15 resistance genes, many of which were located on mobile genetic elements. ICE<sub>WUSP082–1</sub> carries <em>tet(O)</em>, <em>erm(B)</em>, and <em>ant(6)-Ia</em>, showing 99.10 % sequence similarity to <em>S. suis</em> ICE<sub>SsuZJ20091101–1</sub>. GI<sub>WUSP082–1</sub>, containing <em>tet(L)</em> and <em>tet(M)</em>, shares 99.94 % similarity with <em>S. suis</em> 89-kb pathogenicity island. Plasmid<sub>WUSP082</sub>, carrying <em>fexA</em>, <em>optrA</em>, and <em>erm(A)</em>, shares 98.85 % sequence homology with <em>Enterococcus faecium</em> plasmid pW6–2. All 15 strains collected from our lab displayed multidrug resistance, being resistant to at least four classes of antibiotics. Mouse infection experiments demonstrated the pathogenic potential of WUSP082, isolated from the tonsil of a healthy pig. This study advances our understanding of the genomic characteristics and antimicrobial resistance of <em>S. pasteurianus</em>, offering valuable insights for the surveillance and management of this under-recognized zoonotic pathogen.</div></div>","PeriodicalId":23551,"journal":{"name":"Veterinary microbiology","volume":"303 ","pages":"Article 110428"},"PeriodicalIF":2.7000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genomic characteristics and antimicrobial resistance of the underreported zoonotic pathogen Streptococcus pasteurianus and its co-colonization with Streptococcus suis\",\"authors\":\"Shuoyue Wang , Xinchun Li , Chenxu Zheng , Juan J. Quereda , Jie Sun , Huochun Yao , Zongfu Wu\",\"doi\":\"10.1016/j.vetmic.2025.110428\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Streptococcus pasteurianus</em> is an opportunistic pathogen affecting various animals and is an underreported zoonotic threat. It is also a causative agent of swine streptococcosis and can be co-detected with <em>Streptococcus suis</em>, another significant pig and zoonotic pathogen. However, the dynamics of co-colonization between these pathogens, along with the genomic features and antibiotic resistance profiles of <em>S. pasteurianus</em>, remain poorly understood. In this study, we developed a multiplex PCR (mPCR) assay to detect <em>S. pasteurianus</em> and <em>S. suis</em> in 827 tonsil samples from healthy pigs, with 81 samples positive for both pathogens. Pan-genome analysis revealed an open pan-genome, indicating an adaptable genome. Antibiotic resistance gene analysis identified 21 distinct genes, including the first identification of <em>mef(A)</em>, <em>msr(D)</em>, <em>optrA</em>, <em>lnu(G)</em>, <em>spw</em>, <em>dfrF</em>, and <em>fexA</em> in <em>S. pasteurianus</em>. Strain WUSP082 carried 15 resistance genes, many of which were located on mobile genetic elements. ICE<sub>WUSP082–1</sub> carries <em>tet(O)</em>, <em>erm(B)</em>, and <em>ant(6)-Ia</em>, showing 99.10 % sequence similarity to <em>S. suis</em> ICE<sub>SsuZJ20091101–1</sub>. GI<sub>WUSP082–1</sub>, containing <em>tet(L)</em> and <em>tet(M)</em>, shares 99.94 % similarity with <em>S. suis</em> 89-kb pathogenicity island. Plasmid<sub>WUSP082</sub>, carrying <em>fexA</em>, <em>optrA</em>, and <em>erm(A)</em>, shares 98.85 % sequence homology with <em>Enterococcus faecium</em> plasmid pW6–2. All 15 strains collected from our lab displayed multidrug resistance, being resistant to at least four classes of antibiotics. Mouse infection experiments demonstrated the pathogenic potential of WUSP082, isolated from the tonsil of a healthy pig. This study advances our understanding of the genomic characteristics and antimicrobial resistance of <em>S. pasteurianus</em>, offering valuable insights for the surveillance and management of this under-recognized zoonotic pathogen.</div></div>\",\"PeriodicalId\":23551,\"journal\":{\"name\":\"Veterinary microbiology\",\"volume\":\"303 \",\"pages\":\"Article 110428\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary microbiology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S037811352500063X\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/11 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary microbiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S037811352500063X","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
巴氏链球菌是一种影响多种动物的机会性病原体,是一种未被充分报道的人畜共患威胁。它也是猪链球菌病的病原体,可与猪链球菌(另一种重要的猪和人畜共患病原体)共同检测。然而,这些病原体之间共定植的动态,以及巴氏球菌的基因组特征和抗生素耐药性谱,仍然知之甚少。在本研究中,我们建立了一种多重PCR (mPCR)检测方法,对827份健康猪扁桃体样本进行了巴氏球菌和猪链球菌的检测,其中81份样本中两种病原体均呈阳性。泛基因组分析显示一个开放的泛基因组,表明基因组具有适应性。抗生素耐药基因分析鉴定出21个不同基因,其中首次在巴氏链球菌中鉴定出mef(A)、msr(D)、optrA、lnu(G)、spw、dfrF和fexA。菌株WUSP082携带15个抗性基因,其中许多抗性基因位于移动遗传元件上。ICEWUSP082-1携带tet(O)、erm(B)和ant(6)-Ia,与s.s suis ICESsuZJ20091101-1序列相似度为99.10 %。GIWUSP082-1含有tet(L)和tet(M),与猪链球菌89-kb致病性岛相似度为99.94 %。质粒wusp082携带fexA、optrA和erm(A),与屎肠球菌质粒pW6-2序列同源性为98.85 %。从我们实验室收集的所有15株菌株都显示出多重耐药性,对至少四类抗生素具有耐药性。小鼠感染实验表明,从健康猪扁桃体中分离的WUSP082具有致病性。本研究促进了我们对巴氏球菌的基因组特征和耐药性的理解,为这种未被充分认识的人畜共患病原体的监测和管理提供了有价值的见解。
Genomic characteristics and antimicrobial resistance of the underreported zoonotic pathogen Streptococcus pasteurianus and its co-colonization with Streptococcus suis
Streptococcus pasteurianus is an opportunistic pathogen affecting various animals and is an underreported zoonotic threat. It is also a causative agent of swine streptococcosis and can be co-detected with Streptococcus suis, another significant pig and zoonotic pathogen. However, the dynamics of co-colonization between these pathogens, along with the genomic features and antibiotic resistance profiles of S. pasteurianus, remain poorly understood. In this study, we developed a multiplex PCR (mPCR) assay to detect S. pasteurianus and S. suis in 827 tonsil samples from healthy pigs, with 81 samples positive for both pathogens. Pan-genome analysis revealed an open pan-genome, indicating an adaptable genome. Antibiotic resistance gene analysis identified 21 distinct genes, including the first identification of mef(A), msr(D), optrA, lnu(G), spw, dfrF, and fexA in S. pasteurianus. Strain WUSP082 carried 15 resistance genes, many of which were located on mobile genetic elements. ICEWUSP082–1 carries tet(O), erm(B), and ant(6)-Ia, showing 99.10 % sequence similarity to S. suis ICESsuZJ20091101–1. GIWUSP082–1, containing tet(L) and tet(M), shares 99.94 % similarity with S. suis 89-kb pathogenicity island. PlasmidWUSP082, carrying fexA, optrA, and erm(A), shares 98.85 % sequence homology with Enterococcus faecium plasmid pW6–2. All 15 strains collected from our lab displayed multidrug resistance, being resistant to at least four classes of antibiotics. Mouse infection experiments demonstrated the pathogenic potential of WUSP082, isolated from the tonsil of a healthy pig. This study advances our understanding of the genomic characteristics and antimicrobial resistance of S. pasteurianus, offering valuable insights for the surveillance and management of this under-recognized zoonotic pathogen.
期刊介绍:
Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal.
Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge.
Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.