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. 2012 Apr 1;12:80. doi: 10.1186/1471-2334-12-80

Using sequence data to identify alternative routes and risk of infection: a case-study of campylobacter in Scotland

Paul R Bessell 1,6,✉, Ovidiu Rotariu 2, Giles T Innocent 1, Alison Smith-Palmer 3, Norval JC Strachan 2, Ken J Forbes 4, John M Cowden 3, Stuart WJ Reid 5, Louise Matthews 1
PMCID: PMC3340322  PMID: 22462563

Abstract

Background

Genetic typing data are a potentially powerful resource for determining how infection is acquired. In this paper MLST typing was used to distinguish the routes and risks of infection of humans with Campylobacter jejuni from poultry and ruminant sources

Methods

C. jejuni samples from animal and environmental sources and from reported human cases confirmed between June 2005 and September 2006 were typed using MLST. The STRUCTURE software was used to assign the specific sequence types of the sporadic human cases to a particular source. We then used mixed case-case logistic regression analysis to compare the risk factors for being infected with C. jejuni from different sources.

Results

A total of 1,599 (46.3%) cases were assigned to poultry, 1,070 (31.0%) to ruminant and 67 (1.9%) to wild bird sources; the remaining 715 (20.7%) did not have a source that could be assigned with a probability of greater than 0.95. Compared to ruminant sources, cases attributed to poultry sources were typically among adults (odds ratio (OR) = 1.497, 95% confidence intervals (CIs) = 1.211, 1.852), not among males (OR = 0.834, 95% CIs = 0.712, 0.977), in areas with population density of greater than 500 people/km2 (OR = 1.213, 95% CIs = 1.030, 1.431), reported in the winter (OR = 1.272, 95% CIs = 1.067, 1.517) and had undertaken recent overseas travel (OR = 1.618, 95% CIs = 1.056, 2.481). The poultry assigned strains had a similar epidemiology to the unassigned strains, with the exception of a significantly higher likelihood of reporting overseas travel in unassigned strains.

Conclusions

Rather than estimate relative risks for acquiring infection, our analyses show that individuals acquire C. jejuni infection from different sources have different associated risk factors. By enhancing our ability to identify at-risk groups and the times at which these groups are likely to be at risk, this work allows public health messages to be targeted more effectively. The rapidly increasing capacity to conduct genetic typing of pathogens makes such traced epidemiological analysis more accessible and has the potential to substantially enhance epidemiological risk factor studies.

Background

Epidemiological risk factor analyses are used to identify factors that influence the risk of individuals acquiring a particular infection. Such risk factor analyses commonly assume that the risk factors associated with different sources of exposure to infection are homogeneous [1-3]. However, in many cases there are multiple sources of infection and different risk factors may be associated with the different sources. Backward-tracing data on the sources of infection could be used to ascribe different risks to different sources of exposure.

Infection with C. jejuni can be acquired from consumption of contaminated food as well as through direct and indirect contact with animal faeces and has multiple hosts including poultry, ruminants and wild birds [4,5]. Recent developments in the typing of Campylobacter bacteria permits the tracing of sources of infection for human cases of Campylobacteriosis [6]. Campylobacter can be classified by their allelic profile using Multi-Locus-Sequence-Type (MLST) typing techniques [7], which places isolates into specific Sequence Type (ST) profiles. Using STRUCTURE software [8] it is possible to calculate a probability of the ST originating from a particular species [6,9].

Previous studies have identified an association between human C. jejuni infection in Scotland and lower social deprivation score (indicating lower social deprivation) and being a child living in an area of lower population density [10]. A recent study in New Zealand [11] typed C. jejuni isolates using MLST and used the Asymmetric Island probabilistic genetic attribution model [12] to divide these types into ruminant and poultry origin types. Logistic regression analysis of the two types demonstrated that cases of ruminant origin were more likely to occur in rural areas relative to those of poultry origin [11]. A similar methodology will be used in this paper to build on the risk factor analysis of Bessell et al. [10] by differentiating between the risks associated with different sources of infection. For example, one potential explanation for the association found by Bessell et al. [10] with lower deprivation could be differences in access to outdoor leisure activities. If this were the case, it might result in the less deprived being more exposed to ruminant strains should there be greater exposure to ruminant types in the environment.

By comparing the risk factors that are associated with infection by ruminant or poultry associated types, this paper will investigate the value of genetic data, in this instance MLST, to quantify differences in risks associated with different sources. The following hypotheses will be tested:

1. Infection with ruminant strains is more common in rural areas with a large ruminant population.

2. Infection with ruminant types is more associated with lower deprivation than infection with poultry types.

3. Infection with ruminant types is more common in summer relative to poultry types.

4. Infection with ruminant types is more common among children rather than adults relative to poultry types.

5. Infection with ruminant types is associated with domestic exposures whilst poultry attributed infections more commonly result from exposure to exotic types overseas.

Methods

Data

Anonymised reports of laboratory confirmed, passively reported C. jejuni infections were collected by staff at Health Protection Scotland (HPS) from the Public Health Teams at the 12 mainland NHS Health Boards that existed in Scotland prior to 2006. Ethical approval for the collection and use of the data was obtained from the Multi-Centre Research Ethics Committee (MREC) in Scotland; additionally, approval for the research was obtained from the Research and Development Committee in each of the NHS Health Boards. Cases that were confirmed between June 2005 and September 2006 were typed using MLST [6,7]. Typing data was linked to epidemiological and demographic data, where available. The data included the postcode sector of the main residence of the case and either the date of onset or more commonly the date of laboratory report. Cases that were part of an outbreak were excluded and of the remainder, 101 cases were missing a verifiable postcode; these were excluded, leaving 3,834 cases. A further 2 cases had no data on gender and 9 had no record of age; these were also removed leaving 3,823 cases.

In a recent study, we collected samples of C. jejuni from food and environmental sources including chicken, pate and liver, farms with ruminant livestock, livestock faeces, wild bird faeces and urban areas where animal faeces and humans coincide, such as parks [9]. C. jejuni were isolated from these samples and typed using MLST. Subsequently each isolated ST was assigned a probability of originating from a particular source - either poultry, cattle, sheep, wild birds, water and environmental based on their occurrence in each source [6]. The probabilities were assigned using the STRUCTURE software [8]. Each of 441 STs isolated from the 3,451 human cases of C. jejuni (372 cases that were infected with C. coli were removed from the analysis) was assigned a probability that the ST originated from poultry, cattle, sheep, wild bird and environmental sources as described in Sheppard et al. [6]. STs were assigned to ruminant (cattle and sheep), poultry or wild bird whenever the probability for that species was greater than 0.95; otherwise the case remained unassigned. Very few cases were assigned to environmental or swine origin, so these sources were excluded [6]. Cattle and sheep were merged to form a single ruminant category because Ogden et al. [13] demonstrated that there are no significant differences between probabilities assigned to cattle compared to probabilities assigned to sheep and therefore the two sources are indistinguishable in terms of their C. jejuni sequence types.

Logistic regression

Three separate case-case logistic regression analyses were carried out for all combinations of source of infection assignments. As this is a case-case analysis the group used for the base of comparison in the logistic regression are referred to as 'controls' despite them being incidences of disease:

1. Individuals infected with a poultry assigned type (cases) versus individuals infected with a ruminant assigned type (controls).

2. Individuals infected with an unassigned type (cases) versus individuals infected with a ruminant assigned type (controls).

3. Individuals infected with a poultry assigned type (cases) versus individuals infected with an unassigned type (controls).

As the data points are individual cases, case-specific data could be included. Such data include the age, gender and time of year of laboratory reports. The following putative risk factors were included in these analyses:

• The Carstairs deprivation score of the postcode sector [14] (larger values represent greater deprivation) taken from the 2001 Scottish census [15].

• Easting and northing of the postcode sector centroid.

• Population density (people/km2) of the postcode sector using population data from the 2001 Scottish census [15]. This was split to a binary predictor based around a cut-off of 500 people/km2.

• Density of cattle, sheep and poultry (head/km2) in the postcode sector from the June 2004 agricultural census (EDINA, http://edina.ac.uk/agcensus, 2004 estimates).

• Gender (Female reference level)

• Age: Adult/Child (Adult reference level). Children defined as being 18 and under.

• Season in which infection reported: Summer/Winter (Summer reference level). Summer 15 April to 15 October.

• Reporting of recent overseas travel.

To allow for the clustering of certain predictors at the level of 749 postcode sectors, the postcode sector is entered as a random effect. Furthermore, the data were gathered by the 12 mainland NHS Health Boards, so this was entered as a second random effect. Following univariate screening all predictors that were significant at p < 0.25 were entered into a multivariable model which was subsequently reduced by excluding the least significant predictors in turn until only those which were significant at p < 0.05 remained. The effect of removing predictors on the remaining p-values was monitored. Sensitivity analysis checked for the effect of the source assignment cut -off probability by repeating the analysis for a range of cut-off probabilities from 0.5 to 1 and testing for significant change in the risk factors in the final reduced model. Multilevel logistic regression analysis was carried out using the lme4 package [16] in the R statistical environment [17].

Results

Attribution

For a cut-off probability close to 1 the majority of STs can not be assigned to a source of origin (Figure 1A). Relative to the increase in number of wild bird STs as the cut-off probability falls, the number of ruminant and poultry assigned STs increases more slowly (Figure 1A). However, the number of cases assigned to each origin is relatively robust to the choice of cut-off probability (Figure 1B). The majority of cases were assigned to poultry sources (46.4%); 31.0% were assigned a ruminant source whilst 20.7% did not have a source with greater than 0.95 probability (Table 1; Figure 1B). Cases resulting from STs attributed to wild bird sources are very few (1.9%). This does not resemble the distribution of STs, the majority of which (61.3%) were not assigned to a source. Overall, there were 2.6 cases per ST, whereas for poultry and ruminant attributed STs there was a mean of 16.5 and 21.8 cases per ST (Table 1).

Figure 1.

Figure 1

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Source assignment by cut-off probability. The breakdown of the number of unique ST isolates assigned to each source (Figure 1A) and the numbers of cases assigned to each source (Figure 1B). Poultry sources are represented by blue bars, ruminant sources by red bars, wild bird sources by green bars) and unassigned by grey bars. As the cut-off source probability decreases, the number of unassigned STs and cases declines.

Table 1.

The numbers of cases and STs assigned to different sources based upon a probability of greater than 0.95

Attribution Number of cases (%) Number of STs (%) Cases per ST
Poultry 1599 (46.3) 97 (22.0) 16.5
Ruminant 1070 (31.0) 49 (11.1) 21.8
Wild bird 67 (1.9) 22 (5.0) 3.0
Unassigned 715 (20.7) 273 (61.9) 2.6
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Logistic regression analysis

Compared to ruminant assigned cases, poultry assigned cases are more common in winter, in adults, in females, in postcode sectors with population densities greater than 500 people/km2 and more common in individuals reporting overseas travel (Table 2). Relative to ruminant assigned cases, unassigned cases were also more common in winter and in adults, more common in individuals reporting overseas travel (Table 3), and there was an interaction between season and population density such that there was a stronger seasonal effect among unassigned cases in areas of high population density (Table 3; Figure 2). The only significant risk factor for being a poultry assigned case compared to an unassigned case was overseas travel (OR = 0.318, 95% CIs = 0.231, 0.439) and therefore no further results are presented. Additionally the results were tested for sensitivity to the choice of cut off probability for assignment of STs to a source, but adjusting this had no significant effect on the model.

Table 2.

Logistic regression comparing risk factors for being infected by a ruminant attributed type (control) with those for a poultry attributed type (case)

Predictor Unit OR (95% CIs) z-value p-value
Intercept NA 0.213 0.831
Age Child 1 - -
Adult 1.497 (1.211, 1.852) 3.772 < 0.001
Season Summer 1 - -
Winter 1.272 (1.067, 1.517) 2.678 0.007
Sex Female 1 - -
Male 0.834 (0.712, 0.977) -2.248 0.025
Overseas travel No 1
Yes 1.618 (1.056, 2.481) 2.212 0.021
Population dens < = 500/km2 1 - -
> 500/km2 1.213 (1.030, 1.431) 2.313 0.027
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Table 3.

Logistic regression comparing risk factors for being infected by a ruminant attributed type (control) with those for an unassigned type (case).

Predictor Unit OR (95% CIs) z-value p-value
Intercept NA 8.094 < 0.001
Age Child 1 - -
Adult 1.524 (1.156, 2.008) 2.994 0.003
Season Summer 1 - -
Winter 1.919 (1.399, 2.632) 4.035 < 0.001
Overseas travel No 1
Yes 4.808 (3.165, 7.299) 7.377 < 0.001
Population dens < = 500/km2 1 - -
> 500/km2 1.359 (1.071, 1.724) 2.520 0.012
Season * pop.dens Summer * < = 500/km2 1 - -
winter * > 500/km2 0.605 (0.395, 0.926) -2.316 0.021
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Figure 2.

Figure 2

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Case origin by season. The proportion of cases with unassigned or ruminant origins broken down by season and population density corresponding with the interaction in Table 3. Lines represent 95% binomial confidence intervals.

Discussion

By using the MLST technique to attribute isolates from C. jejuni cases to host sources [6], this paper has demonstrated that risk factors for infection depend upon the source of the pathogen. Whilst there is a range of potential sources of C. jejuni infections, this paper has demonstrated that human infections of C. jejuni that are attributable to sources in ruminants are more seasonal and occur more in rural areas than those assigned to poultry sources. Those that were unassigned had very similar epidemiologies to the poultry attributable types.

The work of Sheppard et al. [6] on assigning source probabilities to individual STs has made this analysis possible and it demonstrates that the majority of human cases were attributable to sources in poultry and ruminants or were unassigned (Table 1). However, the majority of STs were not assigned to a source of infection with a probability of greater than 95%. This is in part reflects the large number of STs that represented a small proportion of human infections (Table 1 Figure 1), and suggests that there are either a large number of C. jejuni to which humans have low susceptibility or to which humans are rarely exposed. Consequently, changes in human behaviour or environmental exposures could result in exposure to a large additional pool of bacteria. Twenty-two C. jejuni STs were assigned to wild bird origins, but there were only in 67 reported human cases assigned to an origin in wild birds. This suggests that whilst wild birds are a reservoir there is little mechanism for human exposure, although exposure to preschool children in playgrounds has been suggested elsewhere [18].

The comparisons of poultry attributed cases, ruminant attributed cases and unassigned cases (Tables 2 and 3) showed that ruminant assigned types were more common in children in rural areas in summertime. This may reflect a tendency to play outdoors in the summertime coupled with poor hygiene after playing outdoors. Strachan et al. [19] find similar results and attribute the differences to the consumption of contaminated chicken in urban areas and playing outdoors in rural areas. These findings are similar to those from New Zealand [11], although our larger sample size has enabled us to show that younger age groups in rural areas are at greater risk of infection with a ruminant types in addition to the effect of season. Thus, the heterogeneities in exposure to infection of C. jejuni are consistent across different countries, with similar mechanisms of infection occurring in all, despite the fact that the most common ST in New Zealand that is associated with poultry (ST474) differs from that in Scotland (ST257).

Previous studies [1,10] have identified an association with increased incidence in younger individuals that live in more rural settings. This paper suggests that this is likely to be the result of infection with ruminant types, thus underlining the importance of identifying different sources of infections. Here, the density of the human population rather than the density of cattle and sheep has been identified as the measure of risk for infection with ruminant strains. This suggests that either population density is a better measure of exposure to ruminant sources or that it is some property of rural areas that determines the risk. One such property has been demonstrated to be consumption of water from untreated sources [20]. It is likely that consumption of water from private water sources will be greater in rural areas with lower population densities. ST45 was identified as a type that was associated with surface water sources during a period in the summer [20], however, in this study ST45 was attributed to sources in poultry.

This study did not demonstrate any difference in the risk associated with deprivation for different sources of infection. The relationship between campylobacteriosis and deprivation has been noted in Scotland [10], Denmark [1] and New Zealand [21], but the non-significance of deprivation in this study suggests that deprivation does not influence exposure to environmental sources.

The unassigned types had similar epidemiologies to the poultry types with the consequence that the only significant risk factors for being infected with a poultry rather than an unassigned type was overseas travel. This suggests that the majority of these unassigned types had a similar epidemiology to the poultry types, but insufficient isolates were found in the source assignment to demonstrate their origin and the association with overseas travel suggests that these may be exotic types. Bessell et al. [10] describe a higher likelihood of reporting infection in areas of lower deprivation and lower population density. These analyses show that the effect of rurality may be the signature of the ruminant origin cases.

By using a case-case approach this study did not seek to estimate population level risk of exposure. Rather this study analysed the subgroup of the population that has already been infected, with the principal risk factor being social deprivation [10]. Case-case analysis is a means of comparing risk factors within this sub-group of the population that has acquired infection [22] and has been employed elsewhere for comparing risk factors for infection between sources of C. jejuni [23]. As such, social deprivation remains the principal population level determinant of infection with C. jejuni but these analyses demonstrate that this does not vary between sources of infection.

Conclusions

Our results have demonstrated that over and above the previously demonstrated risk factors for infection at the population level [10], there are different risk factors for infection depending upon the sources of exposure to infection. Therefore, it is important to account for the source of infection in public health planning. The individuals that report infection depend upon the source of C. jejuni, with ruminant exposures more common among the young males in rural areas. For common genetic types, this analysis could be expanded to examine transmission routes that are specific to individual strains. By enhancing our ability to identify at-risk groups and the likely times at which these groups are at risk, public health messages can be targeted more effectively. The rapidly increasing capacity to conduct genetic typing of pathogens makes such traced epidemiological analysis more accessible and has the potential to substantially enhance epidemiological risk factor studies.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

PRB carried out data analysis and drafted the manuscript. OR, NJCS and KJF participated in the cleaning and processing of the MLST data. GTI assisted with statistical analysis and participated in the drafting of the manuscript. ASP and JMC gathered, participated in the cleaning and processing of the Campylobacter case data and assisted with specific public health aspects of the study. SWJR participated in the design and coordination of the study. LM participated in the design and guidance of the study and drafting of the manuscript. All authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2334/12/80/prepub

Contributor Information

Paul R Bessell, Email: paul.bessell@roslin.ed.ac.uk.

Ovidiu Rotariu, Email: ovidiu.rotariu@abdn.ac.uk.

Giles T Innocent, Email: giles@bioss.sari.ac.uk.

Alison Smith-Palmer, Email: alison.smith-palmer@nhs.net.

Norval JC Strachan, Email: n.strachan@abdn.ac.uk.

Ken J Forbes, Email: k.forbes@abdn.ac.uk.

John M Cowden, Email: John.Cowden@hps.scot.nhs.uk.

Stuart WJ Reid, Email: swjreid@rvc.ac.uk.

Louise Matthews, Email: Louise.Matthews@glasgow.ac.uk.

Acknowledgements

The authors are grateful to the Food Standards Agency of Scotland for funding this study.

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