Literature DB >> 34338549

Both Coinfection and Superinfection Drive Complex Anaplasma marginale Strain Structure in a Natural Transmission Setting.

Roberta Koku1, David R Herndon2, Johannetsy Avillan3, Jillian Morrison4, James E Futse5, Guy H Palmer3, Kelly A Brayton1, Susan M Noh1,2,3.   

Abstract

Vector-borne pathogens commonly establish multistrain infections, also called complex infections. How complex infections are established, either before or after the development of an adaptive immune response, termed coinfection or superinfection, respectively, has broad implications for the maintenance of genetic diversity, pathogen phenotype, epidemiology, and disease control strategies. Anaplasma marginale, a genetically diverse, obligate, intracellular, tick-borne bacterial pathogen of cattle, commonly establishes complex infections, particularly in regions with high transmission rates. Both coinfection and superinfection can be established experimentally; however, it is unknown how complex infections develop in a natural transmission setting. To address this question, we introduced naive animals into a herd in southern Ghana with a high infection prevalence and high transmission pressure and tracked the strain acquisition of A. marginale through time using multilocus sequence typing. As expected, the genetic diversity among strains was high, and 97% of animals in the herd harbored multiple strains. All the introduced naive animals became infected, and three to four strains were typically detected in an individual animal prior to seroconversion, while one to two new strains were detected in an individual animal following seroconversion. On average, the number of strains acquired via superinfection was 16% lower than the number acquired via coinfection. Thus, while complex infections develop via both coinfection and superinfection, coinfection predominates in this setting. These findings have broad implications for the development of control strategies in high-transmission settings.

Entities:  

Keywords:  Anaplasma marginale; bovine anaplasmosis; multistrain infections; superinfection; tick-borne disease

Mesh:

Year:  2021        PMID: 34338549      PMCID: PMC8519290          DOI: 10.1128/IAI.00166-21

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.609


  38 in total

Review 1.  The ecology of genetically diverse infections.

Authors:  A F Read; L H Taylor
Journal:  Science       Date:  2001-05-11       Impact factor: 47.728

2.  Structural Basis for Recombinatorial Permissiveness in the Generation of Anaplasma marginale Msp2 Antigenic Variants.

Authors:  Telmo Graça; Marta G Silva; Alla S Kostyukova; Guy H Palmer
Journal:  Infect Immun       Date:  2016-09-19       Impact factor: 3.441

3.  Coinfection and the evolution of parasite virulence.

Authors:  R M May; M A Nowak
Journal:  Proc Biol Sci       Date:  1995-08-22       Impact factor: 5.349

4.  Stochastic transmission of multiple genotypically distinct Anaplasma marginale strains in a herd with high prevalence of Anaplasma infection.

Authors:  Guy H Palmer; Donald P Knowles; Jose-Luis Rodriguez; David P Gnad; Larry C Hollis; Twig Marston; Kelly A Brayton
Journal:  J Clin Microbiol       Date:  2004-11       Impact factor: 5.948

5.  Factors associated with seroprevalence of bovine anaplasmosis in Mississippi, USA.

Authors:  Chika C Okafor; Samantha L Collins; Joseph A Daniel; Johann F Coetzee; Brian K Whitlock
Journal:  Vet Parasitol Reg Stud Reports       Date:  2019-04-26

6.  Frequency of antibodies to Babesia bigemina, B. bovis, Anaplasma marginale, Trypanosoma vivax and Borrelia burgdorferi in cattle from the Northeastern region of the State of Pará, Brazil.

Authors:  Daniel S Guedes; Flábio R Araújo; Fábio J M Silva; Charles P Rangel; José D Barbosa Neto; Adivaldo H Fonseca
Journal:  Rev Bras Parasitol Vet       Date:  2008 Apr-Jun

7.  Tick-borne transmission of two genetically distinct Anaplasma marginale strains following superinfection of the mammalian reservoir host.

Authors:  Christina K Leverich; Guy H Palmer; Donald P Knowles; Kelly A Brayton
Journal:  Infect Immun       Date:  2008-06-23       Impact factor: 3.441

8.  Superinfection Exclusion of the Ruminant Pathogen Anaplasma marginale in Its Tick Vector Is Dependent on the Time between Exposures to the Strains.

Authors:  Susan M Noh; Michael J Dark; Kathryn E Reif; Massaro W Ueti; Lowell S Kappmeyer; Glen A Scoles; Guy H Palmer; Kelly A Brayton
Journal:  Appl Environ Microbiol       Date:  2016-05-16       Impact factor: 4.792

9.  Anaplasma marginale superinfection attributable to pathogen strains with distinct genomic backgrounds.

Authors:  Eduardo Vallejo Esquerra; David R Herndon; Francisco Alpirez Mendoza; Juan Mosqueda; Guy H Palmer
Journal:  Infect Immun       Date:  2014-10-06       Impact factor: 3.441

10.  Dual HIV-1 infection associated with rapid disease progression.

Authors:  Geoffrey S Gottlieb; David C Nickle; Mark A Jensen; Kim G Wong; Jandre Grobler; Fusheng Li; Shan-Lu Liu; Cecilia Rademeyer; Gerald H Learn; Salim S Abdool Karim; Carolyn Williamson; Lawrence Corey; Joseph B Margolick; James I Mullins
Journal:  Lancet       Date:  2004-02-21       Impact factor: 79.321

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