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Identifying the Age Cohort Responsible for Transmission in a Natural Outbreak of


Identifying the major routes of disease transmission and reservoirs of infection are needed to increase our understanding of disease dynamics and improve disease control. Despite this, transmission events are rarely observed directly. Here we had the unique opportunity to study natural transmission of Bordetella bronchiseptica – a directly transmitted respiratory pathogen with a wide mammalian host range, including sporadic infection of humans – within a commercial rabbitry to evaluate the relative effects of sex and age on the transmission dynamics therein. We did this by developing an a priori set of hypotheses outlining how natural B. bronchiseptica infections may be transmitted between rabbits. We discriminated between these hypotheses by using force-of-infection estimates coupled with random effects binomial regression analysis of B. bronchiseptica age-prevalence data from within our rabbit population. Force-of-infection analysis allowed us to quantify the apparent prevalence of B. bronchiseptica while correcting for age structure. To determine whether transmission is largely within social groups (in this case litter), or from an external group, we used random-effect binomial regression to evaluate the importance of social mixing in disease spread. Between these two approaches our results support young weanlings – as opposed to, for example, breeder or maternal cohorts – as the age cohort primarily responsible for B. bronchiseptica transmission. Thus age-prevalence data, which is relatively easy to gather in clinical or agricultural settings, can be used to evaluate contact patterns and infer the likely age-cohort responsible for transmission of directly transmitted infections. These insights shed light on the dynamics of disease spread and allow an assessment to be made of the best methods for effective long-term disease control.


Vyšlo v časopise: Identifying the Age Cohort Responsible for Transmission in a Natural Outbreak of. PLoS Pathog 6(12): e32767. doi:10.1371/journal.ppat.1001224
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1001224

Souhrn

Identifying the major routes of disease transmission and reservoirs of infection are needed to increase our understanding of disease dynamics and improve disease control. Despite this, transmission events are rarely observed directly. Here we had the unique opportunity to study natural transmission of Bordetella bronchiseptica – a directly transmitted respiratory pathogen with a wide mammalian host range, including sporadic infection of humans – within a commercial rabbitry to evaluate the relative effects of sex and age on the transmission dynamics therein. We did this by developing an a priori set of hypotheses outlining how natural B. bronchiseptica infections may be transmitted between rabbits. We discriminated between these hypotheses by using force-of-infection estimates coupled with random effects binomial regression analysis of B. bronchiseptica age-prevalence data from within our rabbit population. Force-of-infection analysis allowed us to quantify the apparent prevalence of B. bronchiseptica while correcting for age structure. To determine whether transmission is largely within social groups (in this case litter), or from an external group, we used random-effect binomial regression to evaluate the importance of social mixing in disease spread. Between these two approaches our results support young weanlings – as opposed to, for example, breeder or maternal cohorts – as the age cohort primarily responsible for B. bronchiseptica transmission. Thus age-prevalence data, which is relatively easy to gather in clinical or agricultural settings, can be used to evaluate contact patterns and infer the likely age-cohort responsible for transmission of directly transmitted infections. These insights shed light on the dynamics of disease spread and allow an assessment to be made of the best methods for effective long-term disease control.


Zdroje

1. WoolhouseME

DyeC

EtardJF

SmithT

CharlwoodJD

1997 Heterogeneities in the transmission of infectious agents: implications for the design of control programs. Proc Natl Acad Sci U S A 94 338 342

2. AndersonRM

MayRM

1991 Infectious Diseases of Humans: Dynamics and Control: Oxford Oxford University Press

3. KlepacP

PomeroyLW

BjornstadON

KuikenT

OsterhausAD

2009 Stage-structured transmission of phocine distemper virus in the Dutch 2002 outbreak. Proc Biol Sci 276 2469 2476

4. McCallumH

BarlowN

HoneJ

2001 How should pathogen transmission be modelled? Trends Ecol Evol 16 295 300

5. PerkinsSE

CattadoriIM

TagliapietraV

RizzoliAP

HudsonPJ

2003 Empirical evidence for key hosts in persistence of a tick-borne disease. Int J Parasitol 33 909 917

6. EamesKT

KeelingMJ

2003 Contact tracing and disease control. Proc Biol Sci 270 2565 2571

7. MuenchH

1959 Catalytic Models in Epidemiology. Harvard University Press

8. HensN

AertsM

FaesC

ShkedyZ

LejeuneO

Seventy-five years of estimating the force of infection from current status data. Epidemiol Infect 138 802 812

9. GriffithsDA

1974 A catalytic model of infection for measles. Applied Statistics 23 330 339

10. AndersonRM

MayRM

1985 Age-related changes in the rate of disease transmission: implications for the design of vaccination programmes. Journal of Hygiene 94 365 436

11. GrenfellBT

AndersonRM

1985 The estimation of age-related rates of infection from case notifications and serological data. J Hygiene 95 419 436

12. FarringtonCP

1990 Modelling forces of infection for measles, mumps and rubella. Statistics in Medicine 9 953 967

13. KeidingN

1991 Age-specific incidence and prevalence: a statistical perspective. Journal of the Royal Statistical Society, Series B 154 371 412

14. CaleyP

HoneJ

2002 Estimating the force-of-infection; Mycobacterium bovis infection in feral ferrets Mustela furo in New Zealand. J Animal Ecol 71 44 54

15. HeiseyDM

JolyDO

MessierFO

2006 The fitting of general Force-Of-Infection models to wildlife disease prevalence data Ecology 87 2356 2365

16. CornellSJ

BjornstadON

CattadoriIM

BoagB

HudsonPJ

2008 Seasonality, cohort-dependence and the development of immunity in a natural host-nematode system. Proc Biol Sci 275 511 518

17. CattadoriIM

BoagB

BjornstadON

CornellSJ

HudsonPJ

2005 Peak shift and epidemiology in a seasonal host-nematode system. Proc Biol Sci 272 1163 1169

18. GauthierDT

LatourRJ

HeiseyDM

BonzekCF

GartlandJ

2008 Mycobacteriosis-associated mortality in wild striped bass (Morone saxatilis) from Chesapeake Bay, U.S.A. Ecol Appl 18 1718 1727

19. OzgulA

OliMK

BolkerBM

Perez-HeydrichC

2009 Upper respiratory tract disease, force of infection, and effects on survival of gopher tortoises. Ecol Appl 19 786 798

20. LairdNM

WareJH

1982 Random-effects models for longitudinal data. Biometrics 38 963 974

21. BolkerBM

BrooksME

ClarkCJ

GeangeSW

PoulsenJR

2009 Generalized Linear Mixed Models: a Practical Guide for Ecology and Evolution. Trends Ecol Evol 24 127 135

22. BjornstadON

HarvillET

2005 Evolution and emergence of Bordetella in humans. Trends Microbiol 13 355 359

23. MattooS

CherryJD

2005 Molecular pathogenesis, epidemiology, and clinical manifestations of respiratory infections due to Bordetella pertussis and other Bordetella subspecies. Clin Microbiol Rev 18 326 382

24. GoodnowRA

1980 Biology of Bordetella bronchiseptica. Microb Rev 44 722 738

25. GlassLS

BeasleyJN

1989 Infection with and antibody response to Pasteurella multocida and Bordetella bronchiseptica in immature rabbits. Lab Anim Sci 39 406 410

26. DeebBJ

DiGiacomoRF

BernardBL

SilbernagelSM

1990 Pasteurella multocida and Bordetella bronchiseptica infections in rabbits. J Clin Microbiol 28 70 75

27. de JongMF

1992 Progressive atrophic rhinitis. In: Diseases of Swine 1: pp. 414-435, Iowa State University Press, Ames, IA

28. PathakAK

CreppageKE

WernerJR

CattadoriIM

2010 Immune regulation of a chronic bacteria infection and consequences for pathogen transmission. BMC Microbiol 10 226

29. PathakAK

BoagB

PossM

HarvillET

CattadoriIM

in press Seasonal Breeding drives the incidence of a chronic bacterial infection in a free-living herbivore population. Infect Epid

30. GuptaS

FergusonN

AndersonR

1998 Chaos, persistence, and evolution of strain structure in antigenically diverse infectious agents. Science 280 912 915

31. ThompsonRCA

2000 Molecular epidemiology of infectious diseases Arnold: London

32. WebsterLT

1924 The epidemiology of a rabbit respiratory infection Il. Clinical, pathological, and bacteriological study of snuffles. J Exp Med 39 843 856

33. JolleyKA

ChanMS

MaidenMC

2004 mlstdbNet - Distributed multi-locus sequence typing (MLST) databases. BMC Bioinformatics 5 86

34. MaidenMC

BygravesJA

FeilE

MorelliG

RussellJE

1998 Multilocus sequence typing: A portable approach to the identification of clones within populations of pathogenic microorganisms. Proc Natl Acad Sci U S A 95 3140 3145

35. DiavatopoulosDA

CummingsCA

SchoulsLM

BrinigMM

RelmanDA

2005 Bordetella pertussis, the causative agent of whooping cough, evolved from a distinct, human-associated lineage of B. bronchiseptica. PLoS Path 1 e45

36. FriedmanM

1982 Piecewise Exponential Models for Survival Data with Covariates. Annals of Statistics 10 101 113

37. BolkerBM

2008 Ecological Models and Data in R: Princeton University Press

38. BurnhamKP

AndersonDR

2002 Model Selection and Multi-Model Inference; A Practical Information - Theoretic Approach. 2: Springer-Verlag, New York

39. VenablesWN

RipleyBD

1994 Modern applied statistics with S-plus. Statistics and Computing

40. SmithIM

GilesCJ

BaskervilleAJ

1982 Immunisation of pigs against experimental infection with Bordetella bronchiseptica. Vet Rec 110 488 494

41. KeelingMJ

WoolhouseME

ShawDJ

MatthewsL

Chase-ToppingM

2001 Dynamics of the 2001 UK foot and mouth epidemic: stochastic dispersal in a heterogeneous landscape. Science 294 813 817

42. WoolhouseM

DonaldsonA

2001 Managing foot-and-mouth. Nature 410 515 516

43. DobsonA

MeagherM

1996 The Population Dynamics of Brucellosis in Yellowstone National Park. Ecology 77 1026 1036

44. AndersonRM

TrewhellaW

1985 Population dynamics of the badger (Meles meles) and the epidemiology of bovine tuberculosis (Mycobacterium bovis). Philos Trans R Soc Lond B Biol Sci 310 327 381

45. JolyDO

MessierF

2004 Factors affecting apparent prevalence of tuberculosis and brucellosis in wood bison. Journal of Animal Ecology 73 623 631

46. SimonV

HoDD

Abdool KarimQ

2006 HIV/AIDS epidemiology, pathogenesis, prevention, and treatment. Lancet 368 489 504

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Hygiena a epidemiológia Infekčné lekárstvo Laboratórium

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