Application of a bespoke monoclonal antibody panel to characterize immune cell populations in cave nectar bats
Among their many unique biological features, bats are increasingly recognized as a key reservoir of many emerging viruses that cause massive morbidity and mortality in humans. Bats are capable of harboring many of these deadly viruses without any apparent signs of pathology, in a mechanism known as...
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Published in | Cell reports (Cambridge) Vol. 43; no. 9; p. 114703 |
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Main Authors | , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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24.09.2024
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Abstract | Among their many unique biological features, bats are increasingly recognized as a key reservoir of many emerging viruses that cause massive morbidity and mortality in humans. Bats are capable of harboring many of these deadly viruses without any apparent signs of pathology, in a mechanism known as viral disease tolerance. However, the immunological mechanisms behind viral tolerance remain poorly understood. As a non-model organism species, there are very limited research resources and tools available to study bat immunology. In the cave nectar bat Eonycteris spelaea, we have a panel of monoclonal antibodies (mAbs) against major immune markers. An immunophenotyping survey of major immune compartments and barrier sites using these mAbs reveals differences in the immunological landscape of bats.
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•Development of a panel of monoclonal antibodies specific to E. spelaea•Flow cytometric phenotyping of multiple tissues to compare bats and mice•Bats have fewer B cells and a skewing of monocytes toward the non-classical lineage•CD4 and CD21 mAbs demonstrate cross-reactivity to two other bat species
Bats are reservoir hosts of many viruses, harboring these viruses using unique mechanisms of viral tolerance. However, immunological study has been impaired by a lack of suitable tools. Chen et al. address this limitation by the usage of a panel of bat-specific monoclonal antibodies for flow cytometry. |
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AbstractList | Among their many unique biological features, bats are increasingly recognized as a key reservoir of many emerging viruses that cause massive morbidity and mortality in humans. Bats are capable of harboring many of these deadly viruses without any apparent signs of pathology, in a mechanism known as viral disease tolerance. However, the immunological mechanisms behind viral tolerance remain poorly understood. As a non-model organism species, there are very limited research resources and tools available to study bat immunology. In the cave nectar bat Eonycteris spelaea, we have a panel of monoclonal antibodies (mAbs) against major immune markers. An immunophenotyping survey of major immune compartments and barrier sites using these mAbs reveals differences in the immunological landscape of bats.
[Display omitted]
•Development of a panel of monoclonal antibodies specific to E. spelaea•Flow cytometric phenotyping of multiple tissues to compare bats and mice•Bats have fewer B cells and a skewing of monocytes toward the non-classical lineage•CD4 and CD21 mAbs demonstrate cross-reactivity to two other bat species
Bats are reservoir hosts of many viruses, harboring these viruses using unique mechanisms of viral tolerance. However, immunological study has been impaired by a lack of suitable tools. Chen et al. address this limitation by the usage of a panel of bat-specific monoclonal antibodies for flow cytometry. Among their many unique biological features, bats are increasingly recognized as a key reservoir of many emerging viruses that cause massive morbidity and mortality in humans. Bats are capable of harboring many of these deadly viruses without any apparent signs of pathology, in a mechanism known as viral disease tolerance. However, the immunological mechanisms behind viral tolerance remain poorly understood. As a non-model organism species, there are very limited research resources and tools available to study bat immunology. In the cave nectar bat Eonycteris spelaea, we have a panel of monoclonal antibodies (mAbs) against major immune markers. An immunophenotyping survey of major immune compartments and barrier sites using these mAbs reveals differences in the immunological landscape of bats. Among their many unique biological features, bats are increasingly recognized as a key reservoir of many emerging viruses that cause massive morbidity and mortality in humans. Bats are capable of harboring many of these deadly viruses without any apparent signs of pathology, in a mechanism known as viral disease tolerance. However, the immunological mechanisms behind viral tolerance remain poorly understood. As a non-model organism species, there are very limited research resources and tools available to study bat immunology. In the cave nectar bat Eonycteris spelaea, we have a panel of monoclonal antibodies (mAbs) against major immune markers. An immunophenotyping survey of major immune compartments and barrier sites using these mAbs reveals differences in the immunological landscape of bats.Among their many unique biological features, bats are increasingly recognized as a key reservoir of many emerging viruses that cause massive morbidity and mortality in humans. Bats are capable of harboring many of these deadly viruses without any apparent signs of pathology, in a mechanism known as viral disease tolerance. However, the immunological mechanisms behind viral tolerance remain poorly understood. As a non-model organism species, there are very limited research resources and tools available to study bat immunology. In the cave nectar bat Eonycteris spelaea, we have a panel of monoclonal antibodies (mAbs) against major immune markers. An immunophenotyping survey of major immune compartments and barrier sites using these mAbs reveals differences in the immunological landscape of bats. |
ArticleNumber | 114703 |
Author | Ng, Wei Lun Smith, Gavin J.D. Chan, Wharton O.Y. Kong, Pui San Tang, Leon J.W. Gamage, Akshamal M. Zhu, Feng Wang, Lin-Fa Lim, Beng Lee Hong, Lewis Z. Loh, Abigail Y.T. Low, Dolyce H.W. Chia, Wanni Foo, Randy Chen, Shiwei He, Shan Tan, Adrian H.J. Kwek, Madeline S.S. Sia, Wan Rong |
Author_xml | – sequence: 1 givenname: Shiwei surname: Chen fullname: Chen, Shiwei organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 2 givenname: Wan Rong surname: Sia fullname: Sia, Wan Rong organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 3 givenname: Leon J.W. surname: Tang fullname: Tang, Leon J.W. organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 4 givenname: Akshamal M. surname: Gamage fullname: Gamage, Akshamal M. organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 5 givenname: Wharton O.Y. surname: Chan fullname: Chan, Wharton O.Y. organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 6 givenname: Feng surname: Zhu fullname: Zhu, Feng organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 7 givenname: Wanni surname: Chia fullname: Chia, Wanni organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 8 givenname: Madeline S.S. surname: Kwek fullname: Kwek, Madeline S.S. organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 9 givenname: Pui San surname: Kong fullname: Kong, Pui San organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 10 givenname: Beng Lee surname: Lim fullname: Lim, Beng Lee organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 11 givenname: Randy surname: Foo fullname: Foo, Randy organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 12 givenname: Wei Lun surname: Ng fullname: Ng, Wei Lun organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 13 givenname: Adrian H.J. surname: Tan fullname: Tan, Adrian H.J. organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 14 givenname: Shan surname: He fullname: He, Shan organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 15 givenname: Abigail Y.T. surname: Loh fullname: Loh, Abigail Y.T. organization: Paratus Sciences, Singapore, Singapore – sequence: 16 givenname: Dolyce H.W. surname: Low fullname: Low, Dolyce H.W. organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 17 givenname: Gavin J.D. surname: Smith fullname: Smith, Gavin J.D. organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore – sequence: 18 givenname: Lewis Z. surname: Hong fullname: Hong, Lewis Z. organization: Paratus Sciences, Singapore, Singapore – sequence: 19 givenname: Lin-Fa orcidid: 0000-0003-2752-0535 surname: Wang fullname: Wang, Lin-Fa email: linfa.wang@duke-nus.edu.sg organization: Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore, Singapore |
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Keywords | CP: Immunology bat monoclonal antibody immunology disease tolerance mAb |
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Title | Application of a bespoke monoclonal antibody panel to characterize immune cell populations in cave nectar bats |
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