Amplicon Sequencing Reveals Complex Infection in Infants Congenitally Infected With Trypanosoma Cruzi and Informs the Dynamics of Parasite Transmission

Author:

Hakim Jill M C1,Waltmann Andreea2,Tinajeros Freddy3,Kharabora Oksana2,Machaca Edith Málaga34,Calderon Maritza4,del Carmen Menduiña María5,Wang Jeremy6ORCID,Rueda Daniel7,Zimic Mirko4,Verástegui Manuela4,Juliano Jonathan J28,Gilman Robert H9,Mugnier Monica R1ORCID,Bowman Natalie M8,

Affiliation:

1. Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health , Baltimore, Maryland , USA

2. Institute for Global Health and Infectious Disease, School of Medicine, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina , USA

3. Asociación Benéfica PRISMA , Lima , Peru

4. Infectious Diseases Research Laboratory, Department of Cellular and Molecular Sciences, Universidad Peruana Cayetano Heredia , Lima , Perú

5. Hospital Percy Boland Rodríguez, Ministerio de Salud Bolivia , Santa Cruz , Bolivia

6. University of North Carolina, Chapel Hill School of Medicine , Chapel Hill, North Carolina , USA

7. Facultad de Ciencias, Universidad Nacional de Ingeniería , Lima , Perú

8. Division of Infectious Diseases, Department of Medicine, University of North Carolina at Chapel Hill School of Medicine , Chapel Hill, North Carolina , USA

9. Department of International Health, Johns Hopkins University Bloomberg School of Public Health , Baltimore, Maryland , USA

Abstract

Abstract Congenital transmission of Trypanosoma cruzi is an important source of new Chagas infections worldwide. The mechanisms of congenital transmission remain poorly understood, but there is evidence that parasite factors are involved. Investigating changes in parasite strain diversity during transmission could provide insight into the parasite factors that influence the process. Here we use amplicon sequencing of a single copy T. cruzi gene to evaluate the diversity of infection in clinical samples from Chagas positive mothers and their infected infants. Several infants and mothers were infected with multiple parasite strains, mostly of the same TcV lineage, and parasite strain diversity was higher in infants than mothers. Two parasite haplotypes were detected exclusively in infant samples, while one haplotype was never found in infants. Together, these data suggest multiple parasites initiate a congenital infection and that parasite factors influence the probability of vertical transmission.

Funder

National Institutes of Health

Doris Duke Charitable Foundation

Sherrilyn and Ken Fisher Center for Environmental and Infectious Disease

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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