Lorena Freitas das Neves , Clara Morato Dias , Anna Claudia Baumel Mongruel , Gabrielly de Oliveira Lopes , Liliane Maria do Rosario Batista , Francisco Anilton Alves Araujo , Gener Tadeu Pereira , Rosangela Zacarias Machado , Marcos Rogério André
{"title":"巴西中西部家养猫(包括献血者)中亨塞拉巴尔通体的人畜共患变异","authors":"Lorena Freitas das Neves , Clara Morato Dias , Anna Claudia Baumel Mongruel , Gabrielly de Oliveira Lopes , Liliane Maria do Rosario Batista , Francisco Anilton Alves Araujo , Gener Tadeu Pereira , Rosangela Zacarias Machado , Marcos Rogério André","doi":"10.1016/j.cimid.2025.102398","DOIUrl":null,"url":null,"abstract":"<div><div><em>Bartonella henselae</em> is a significant zoonotic agent, with domestic cats serving as primary reservoirs. This study investigated the occurrence and genetic diversity of <em>B. henselae</em> in domestic cats from central-western Brazil, including both animals from veterinary clinics and cat blood donors. Serological, microbiological, and molecular techniques were employed. Serum samples were tested using the Indirect Fluorescence Antibody Test (IFAT) to detect anti-<em>B. henselae</em> IgG antibodies. Molecular detection of <em>Bartonella</em> spp. was performed using quantitative real-time PCR (qPCR) targeting the 16–23S rRNA intergenic spacer region, both directly from blood and after enrichment in Bartonella Alpha Proteobacteria Growth Medium (BAPGM). Antibodies were detected in 60.75 % of cats, while qPCR identified <em>Bartonella</em> spp. DNA in 32 % and 46 % of cats from veterinary clinics and blood donors, respectively. Following BAPGM enrichment, 78.2 % of previously negative samples were tested positive by qPCR. Co-positivity in serology and qPCR was observed in 25.3 % of cats. No sample tested positive in all diagnostic methods. Three <em>B. henselae</em> strains were isolated—two from clinic cats and one from a blood donor. Multi-locus sequence typing (MLST) revealed the presence of sequence types ST1, ST2, and ST5. This study is the first to report <em>Bartonella</em> in cat blood donors in South America and the first identification of ST5 in this population. Additionally, ST2 was reported for the first time in cats from the Americas. These findings highlight the potential risk of zoonotic <em>B. henselae</em> transmission via blood transfusion and the limited reliability of serology alone for screening blood donor cats.</div></div>","PeriodicalId":50999,"journal":{"name":"Comparative Immunology Microbiology and Infectious Diseases","volume":"123 ","pages":"Article 102398"},"PeriodicalIF":2.0000,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Zoonotic variants of Bartonella henselae in domesticated cats, including blood donors, in central-western Brazil\",\"authors\":\"Lorena Freitas das Neves , Clara Morato Dias , Anna Claudia Baumel Mongruel , Gabrielly de Oliveira Lopes , Liliane Maria do Rosario Batista , Francisco Anilton Alves Araujo , Gener Tadeu Pereira , Rosangela Zacarias Machado , Marcos Rogério André\",\"doi\":\"10.1016/j.cimid.2025.102398\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Bartonella henselae</em> is a significant zoonotic agent, with domestic cats serving as primary reservoirs. This study investigated the occurrence and genetic diversity of <em>B. henselae</em> in domestic cats from central-western Brazil, including both animals from veterinary clinics and cat blood donors. Serological, microbiological, and molecular techniques were employed. Serum samples were tested using the Indirect Fluorescence Antibody Test (IFAT) to detect anti-<em>B. henselae</em> IgG antibodies. Molecular detection of <em>Bartonella</em> spp. was performed using quantitative real-time PCR (qPCR) targeting the 16–23S rRNA intergenic spacer region, both directly from blood and after enrichment in Bartonella Alpha Proteobacteria Growth Medium (BAPGM). Antibodies were detected in 60.75 % of cats, while qPCR identified <em>Bartonella</em> spp. DNA in 32 % and 46 % of cats from veterinary clinics and blood donors, respectively. Following BAPGM enrichment, 78.2 % of previously negative samples were tested positive by qPCR. Co-positivity in serology and qPCR was observed in 25.3 % of cats. No sample tested positive in all diagnostic methods. Three <em>B. henselae</em> strains were isolated—two from clinic cats and one from a blood donor. Multi-locus sequence typing (MLST) revealed the presence of sequence types ST1, ST2, and ST5. This study is the first to report <em>Bartonella</em> in cat blood donors in South America and the first identification of ST5 in this population. Additionally, ST2 was reported for the first time in cats from the Americas. These findings highlight the potential risk of zoonotic <em>B. henselae</em> transmission via blood transfusion and the limited reliability of serology alone for screening blood donor cats.</div></div>\",\"PeriodicalId\":50999,\"journal\":{\"name\":\"Comparative Immunology Microbiology and Infectious Diseases\",\"volume\":\"123 \",\"pages\":\"Article 102398\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comparative Immunology Microbiology and Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0147957125001067\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Immunology Microbiology and Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0147957125001067","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Zoonotic variants of Bartonella henselae in domesticated cats, including blood donors, in central-western Brazil
Bartonella henselae is a significant zoonotic agent, with domestic cats serving as primary reservoirs. This study investigated the occurrence and genetic diversity of B. henselae in domestic cats from central-western Brazil, including both animals from veterinary clinics and cat blood donors. Serological, microbiological, and molecular techniques were employed. Serum samples were tested using the Indirect Fluorescence Antibody Test (IFAT) to detect anti-B. henselae IgG antibodies. Molecular detection of Bartonella spp. was performed using quantitative real-time PCR (qPCR) targeting the 16–23S rRNA intergenic spacer region, both directly from blood and after enrichment in Bartonella Alpha Proteobacteria Growth Medium (BAPGM). Antibodies were detected in 60.75 % of cats, while qPCR identified Bartonella spp. DNA in 32 % and 46 % of cats from veterinary clinics and blood donors, respectively. Following BAPGM enrichment, 78.2 % of previously negative samples were tested positive by qPCR. Co-positivity in serology and qPCR was observed in 25.3 % of cats. No sample tested positive in all diagnostic methods. Three B. henselae strains were isolated—two from clinic cats and one from a blood donor. Multi-locus sequence typing (MLST) revealed the presence of sequence types ST1, ST2, and ST5. This study is the first to report Bartonella in cat blood donors in South America and the first identification of ST5 in this population. Additionally, ST2 was reported for the first time in cats from the Americas. These findings highlight the potential risk of zoonotic B. henselae transmission via blood transfusion and the limited reliability of serology alone for screening blood donor cats.
期刊介绍:
Comparative Immunology, Microbiology & Infectious Diseases aims to respond to the concept of "One Medicine" and to provide a venue for scientific exchange. Based on the concept of "Comparative Medicine" interdisciplinary cooperation between specialists in human and animal medicine is of mutual interest and benefit. Therefore, there is need to combine the respective interest of physicians, veterinarians and other health professionals for comparative studies relevant to either human or animal medicine .
The journal is open to subjects of common interest related to the immunology, immunopathology, microbiology, parasitology and epidemiology of human and animal infectious diseases, especially zoonotic infections, and animal models of human infectious diseases. The role of environmental factors in disease emergence is emphasized. CIMID is mainly focusing on applied veterinary and human medicine rather than on fundamental experimental research.