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 LaboratóriumČlánok vyšiel v časopise
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