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PLoS Negl Trop Dis. 2010 August; 4(8): e791.
Published online 2010 August 10. doi:  10.1371/journal.pntd.0000791
PMCID: PMC2919402

A Major Role for Mammals in the Ecology of Mycobacterium ulcerans

Jakob Zinsstag, Editor



Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a destructive skin disease found predominantly in sub-Saharan Africa and south-eastern Australia. The precise mode(s) of transmission and environmental reservoir(s) remain unknown, but several studies have explored the role of aquatic invertebrate species. The purpose of this study was to investigate the environmental distribution of M. ulcerans in south-eastern Australia.

Methodology/Principal Findings

A range of environmental samples was collected from Point Lonsdale (a small coastal town southwest of Melbourne, Australia, endemic for BU) and from areas with fewer or no reported incident cases of BU. Mycobacterium ulcerans DNA was detected at low levels by real-time PCR in soil, sediment, water residue, aquatic plant biofilm and terrestrial vegetation collected in Point Lonsdale. Higher levels of M. ulcerans DNA were detected in the faeces of common ringtail (Pseudocheirus peregrinus) and common brushtail (Trichosurus vulpecula) possums. Systematic testing of possum faeces revealed that M. ulcerans DNA could be detected in 41% of faecal samples collected in Point Lonsdale compared with less than 1% of faecal samples collected from non-endemic areas (p<0.0001). Capture and clinical examination of live possums in Point Lonsdale validated the accuracy of the predictive value of the faecal surveys by revealing that 38% of ringtail possums and 24% of brushtail possums had laboratory-confirmed M. ulcerans skin lesions and/or M. ulcerans PCR positive faeces. Whole genome sequencing revealed an extremely close genetic relationship between human and possum M. ulcerans isolates.


The prevailing wisdom is that M. ulcerans is an aquatic pathogen and that BU is acquired by contact with certain aquatic environments (swamps, slow-flowing water). Now, after 70 years of research, we propose a transmission model for BU in which terrestrial mammals are implicated as reservoirs for M. ulcerans.

Author Summary

Mycobacterium ulcerans is the causative agent of Buruli ulcer (BU), a destructive skin disease found predominantly in sub-Saharan Africa and south-eastern Australia. The mode of transmission and environmental reservoir remain unknown, but several studies have explored the role of aquatic insects, such as water bugs, and biting insects, such as mosquitoes. In the present study we investigated possible environmental source(s) of M. ulcerans in Victoria, Australia. Our results revealed that although M. ulcerans DNA could be detected at low levels in a variety of environmental samples, the highest concentrations of M. ulcerans DNA were found in the faeces of two species of possums, common ringtails and common brushtails. Possums are small arboreal marsupial mammals, native to Australia, and these particular species occur in both urban and rural areas. Examination and sampling of live captured possums in an area endemic for BU revealed that 38% of ringtail possums and 24% of brushtail possums, respectively, had laboratory-confirmed M. ulcerans lesions and/or M. ulcerans PCR-positive faeces. The finding that large numbers of possums in a BU-endemic area are infected with M. ulcerans raises the possibility that mammals are an environmental reservoir for M. ulcerans.


Buruli ulcer (BU) is caused by the environmental mycobacterium, Mycobacterium ulcerans. Infection with M. ulcerans often leads to extensive necrosis of the skin and soft tissue with the formation of large ulcers, usually on the leg or arm, due to the production of the destructive polyketide toxin, mycolactone [1]. Although rarely fatal, BU causes serious morbidity and frequently results in permanent disability [2]. The disease has been reported in more than 30 countries worldwide; however, cases mainly occur in regions with tropical and subtropical climates. The majority of cases are found in West and sub-Saharan Africa. Cases of BU often cluster around particular water bodies and are highly focally distributed, with endemic and non-endemic communities often separated by only a few kilometres [2].

Australia is the only developed country reporting significant local transmission of M. ulcerans. In 1948, a cluster of cases linked to the Bairnsdale region in Gippsland was described by McCallum et al. [3]. Since then, foci of infection have been reported in tropical far north Queensland [4] and temperate coastal Victoria, where there have been several outbreaks over the past two decades: Phillip Island (1992–1995), the Frankston/Langwarrin region (1990–1997), St Leonards (2001–2002) and Point Lonsdale (2002-present) (Fig. 1) [5], [6]. The present outbreak in Point Lonsdale, a small coastal town approximately 60 km south-west of the Victorian capital Melbourne, is the largest on record in Australia, with over 100 laboratory-confirmed cases diagnosed since 2002. Geographically, the town is close to sea level, and there are several natural and man-made swamps and water features in the area [6]. Cases of BU have also been described in both native wildlife and domestic mammal species in Victoria, including koalas (Phascolarctos cinereus) [7], common ringtail possums (Pseudocheirus peregrinus) [8], a mountain brushtail possum (Trichosurus cunninghami), a long-footed potoroo (Potorous longipes) (J. Fyfe, unpublished), two horses [9], two dogs (O'Brien et al., manuscript in preparation), an alpaca [8] and a cat [10]. All animal cases were identified in locations where human cases of BU have been reported.

Figure 1
Map of central coastal Victoria, showing places referred to in the text or associated references.

The precise mode(s) of transmission and environmental reservoir(s) of BU are unresolved and continue to be the subject of intense research. Proximity to marshes and wetlands is a recognised risk factor for infection and several studies have explored the role of aquatic invertebrate species as potential vectors and/or reservoirs [6], [11][13]. Detection of M. ulcerans in environmental samples is mainly achieved using PCR, as culturing M. ulcerans directly from the environment is extremely difficult [14]. In Australia, M. ulcerans DNA was detected in water and detritus from swamps during the outbreak of BU on Phillip Island in the mid-1990s [15], [16] and more recently in five species of mosquitoes (Aedes sp., Coquillettidia sp. and Culex sp.) captured from Point Lonsdale (infection rate, 4.3/1,000 mosquitoes) [6]. In West Africa, M. ulcerans DNA has been detected in water and aquatic plants [17], insects (Belastomatidae, Naucoridae, Hydrophilidae), crustaceans and molluscs (Bulinus sp. and Planorbis sp.) and small fish (including Tilapia sp.) [11], [13], [18][21]. Recent studies of the distribution of M. ulcerans in aquatic sites in Ghana found evidence of M. ulcerans DNA in insects, water filtrate, biofilm and soil [12], [13]. In 2008, Portaels et al. described, for the first time, the cultivation and characterisation of an M. ulcerans strain obtained from an aquatic Hemiptera (common name Water Strider, Gerris sp.) from Benin [14].

Analysis of the whole genome sequence of M. ulcerans has provided further insights into the elusive environmental reservoir and mode of transmission [22]. Complete sequencing of an M. ulcerans strain isolated from a patient in Ghana revealed a 5,631,606 bp circular chromosome with 4160 genes, 771 pseudogenes and a 174,155 bp virulence plasmid pMUM001 that is required for the production of mycolactone [23], [24]. Comparison of the M. ulcerans genome with the genome of M. marinum confirmed the very close relationship between these species; however, it also revealed that there are some striking differences, mostly due to the presence of the plasmid pMUM001 and the many chromosomal deletions and rearrangements that have occurred in M. ulcerans [23]. It is therefore likely that M. ulcerans has evolved from an M. marinum-like ancestor by lateral gene transfer and reductive evolution, through the acquisition of a pMUM001-like plasmid, expansion of the two high copy number insertion sequence elements IS2404 and IS2606, extensive gene disintegration (formation of pseudogenes), genome rearrangements and DNA deletion. These characteristics suggest that M. ulcerans has recently passed through a so-called “evolutionary bottleneck” and is adapting to a new, niche environment.

In this study, we investigated potential environmental reservoirs of M. ulcerans in south-eastern Australia with the aim of developing a more comprehensive model of its life cycle and mode of transmission. Specifically, using semi-quantitative real-time PCR and culture to test for the presence of M. ulcerans, we investigated a range of potential abiotic and biotic reservoirs (selected using emerging information in the literature and our own ongoing field based research) in areas of varying BU endemicity. Our findings have led us to propose that M. ulcerans is able to infect small mammals, survive and potentially replicate within their gastrointestinal tracts and raises the possibility that mammals play a major role in the ecology of M. ulcerans.

Materials and Methods

Environmental samples

a. Study sites and sample collection

This study was conducted in Victoria, Australia, primarily at Point Lonsdale on the Bellarine Peninsula (a current human BU outbreak zone, and therefore classified as endemic). A number of other sites, classified as areas of low endemicity (where BU infection has occurred in the past or fewer cases have been recorded recently), or non-endemic (no recorded human or animal BU cases), were also sampled (Fig. 1). The number and types of samples collected and tested are shown in Tables 1 and and2.2. Following collection, all samples were stored in sterile plastic containers or zip-lock bags, transported cool to the laboratory and stored at 4°C prior to DNA extraction, usually within a week of collection.

Table 1
Detection of M. ulcerans DNA (IS2404, IS2606 and KR) in environmental samples collected from Point Lonsdale (endemic) and sites of low endemicity in Victoria, Australia.
Table 2
Detection of M. ulcerans DNA in possum faeces collected from BU high-, low- and non-endemic locations, in Victoria, Australia.

b. Sampling methods

Aquatic environments were sampled for suspended solids/water residue collected from natural and man-made water bodies in Point Lonsdale and low endemicity sites. Two hundred millilitres (ml) of water was passed through a 1.6 micron fibreglass filter (Whatman Inc.) using a hand pump and/or 60–120 ml water through a 1.6 micron fibreglass filter (Whatman Inc.) using a syringe (volume was dependent on turbidity). Aquatic plant biofilms were collected from the dominant macrophytes (plant species) in natural and man-made water bodies, in Point Lonsdale and low endemicity areas, by placing the macrophyte samples in sterile bags, mixing with 200 ml clean water and scrubbing by hand to remove the biofilm. A 50 ml subsample was retained for each. A section of the stem from each macrophyte was also sampled. Aquatic macroinvertebrates were collected by sweeping a handheld D-frame aquatic net through a section of the water body for 45 seconds. Detritus, sediment and soil samples were collected from terrestrial and riparian sites using a hand held plastic sieve or by placing samples directly into a sterile container. Samples from terrestrial vegetation (leaves, bark, flowers, seeds etc) were collected and identified by botanist Neville Walsh (Senior Conservation Botanist, Royal Botanic Gardens, Melbourne).

Faecal samples from common ringtail possums and common brushtail possums (henceforth referred to as ringtail and brushtail possums) were collected directly from the ground, from the branches of trees or from fences, at 100- or 500-metre intervals along transects across areas of varying BU endemicity: Point Lonsdale (high endemicity area); Barwon Heads, Phillip Island, Ocean Grove and Queenscliff (low endemicity areas); Breamlea, metropolitan Melbourne, Boho South and Torquay (non-endemic areas) (Fig. 1). These sampling intervals were chosen to avoid any chance of repeated sampling from the same individual and were based on an estimated home range diameter for ringtail possums of no more than 100 metres (A. Legione, unpublished data). The identity of the animal host was determined by visual identification of the faecal sample (Fig. 2D), by an experienced zoologist (one of the authors) or with the aid of a scat and tracking manual [25].

Figure 2
Photographs of Point Lonsdale, common brushtail possums and common ringtail possums.

Live animal studies

a. Capture and sampling of live possums

The capture of possums, which are nocturnal, was based on standard operating procedures for the handling of wildlife developed by Dr Kath Handasyde, approved by The University of Melbourne Faculty of Veterinary Science Animal Experimentation Ethics Committee (project no. 0706769) and under permit from the Victorian Department of Sustainability and Environment (DSE permit no. 10004406). Cage traps, designed for live capture of brushtail and ringtail possums, baited with an apple smeared with peanut butter or a bait ball of peanut butter and rolled oats, were set 1–2 hours before dark in public and private properties throughout Point Lonsdale and then checked, commencing at dawn, the following morning. Ringtail possums were also caught at night, directly by hand, using a specifically designed noosing pole and a hand-held net. After capture, animals were transferred into material bags, and transported by car to a quiet, enclosed area, awaiting collection of samples and data.

b. Collection of samples and data from live possums

To minimise distress during handling and sampling, possums were heavily sedated with an I.M. injection of Zoletil (Virbac Australia Pty Ltd, 5–8 mg/kg) using a 29 gauge needle. Possums were examined for external lesions resembling BU and, if present, a specimen was obtained by swabbing the affected area. Faecal specimens, along with a number of other clinical samples that are described in a separate report (manuscript in preparation), were also collected. Animals were individually marked, via a number tattooed onto the ear, and a small PIT (passive induction transponder) tag, inserted subcutaneously between the shoulder blades, so that they could be identified in the event of recapture. Individual animals were subjected to full handling only once during any particular field trip. After handling and sampling, animals were placed individually into material bags, and held in an animal box in a quiet enclosed area. Animals were then released at dusk, on the same day, at the site of capture. However, in the circumstance that a captured animal was deemed, by a veterinarian, to be too unwell to be released, there was a provision for the animal to be euthanased using an overdose of pentobarbitone (150mg/kg).

DNA-based analyses

a. DNA preparation

DNA was extracted from samples using the FastDNA® SPIN Kit for Soil with the FastPrep® Instrument (Qbiogene, Inc., Carlsbad, CA), after the following sample-dependent pre-extraction procedures: For soil, sediment, vegetation and possum faeces, ~50–100 mg of wet or dry sample was directly added to the FastPrep Lysing Matrix E tube. Biofilm samples were prepared by centrifuging the Falcon tubes containing the 50 ml subsample at maximum speed for 10 mins. After removing the supernatant, the pellet was resuspended in kit-supplied Sodium Phosphate Buffer and transferred to the Lysing Matrix E tubes. Water residue was prepared by cutting the fibreglass filters into small pieces using a sterile scalpel and adding directly to the Lysing Matrix E tubes. Swabs were placed in sterile bead bottles with 2 ml phosphate buffered saline (PBS), vortexed, and 1 ml added to the Lysing Matrix E tubes. The Lysing Matrix E tubes were then centrifuged at maximum speed for 10 mins and the supernatant removed. After the sample-dependent pre-extraction procedures, DNA extraction was then performed according to the manufacturer's recommendations. DNA preparations were stored at −20°C.

b. Detection of M. ulcerans DNA

DNA extracts were tested for the presence of M. ulcerans DNA using two semi-quantitative real-time PCR assays targeting the insertion sequences IS2404 and IS2606 and a sequence encoding the ketoreductase B domain, KR, within the mlsA1, mlsA2 and mlsB genes. These assays were developed and validated for use on environmental samples by Fyfe et al. [26] and are able to distinguish between M. ulcerans and other mycolactone-producing mycobacteria (MPM) that contain IS2404, but fewer copy numbers of IS2606, based on the difference in cycle threshold values between IS2606 and IS2404CT [IS2606-IS2404]) [26]. All extracts were initially screened singly for the high copy number insertion sequence IS2404. This assay was multiplexed with an internal positive control to monitor PCR inhibition. Inhibited extracts were diluted 1/5 or 1/10 and repeat PCR performed. Extracts that were still inhibited at 1/10 dilution were omitted from analyses. With the exception of the possum faecal samples, all of the IS2404-positive DNA extracts from each sample type were tested in duplicate for IS2606 and KR. In view of the large number of IS2404-positive DNA extracts from possum faecal samples obtained, a subset of these, taken from each of the different locations, was similarly confirmed. The ΔCT (IS2606-IS2404) were calculated to confirm that the sequences detected were attributable to M. ulcerans and not another MPM. To exclude the possibility of contamination, at least one negative control was included in every DNA extraction run, and four negative controls included in every real-time PCR assay.

c. Estimation of M. ulcerans bacterial loads in different samples

To estimate the M. ulcerans bacterial loads (expressed as M. ulcerans/gram or M. ulcerans/ml) in various sample types, the CT values obtained for IS2404 were compared with a standard curve generated using a series of DNA extracts prepared from environmental samples that had been spiked with known numbers of M. ulcerans organisms [26]. These estimates were determined to provide an indication of the relative numbers of M. ulcerans between samples, rather than a strict quantitation of the number of organisms present in a sample, and hence are generally expressed as a 10-fold range.

d. Variable Number Tandem Repeat (VNTR)/Mycobacterial Interspersed Repeat Unit (MIRU) typing

VNTR/MIRU typing was performed using the conditions described previously [27][29] in 25 µl reactions using 1 µl of DNA template. PCR products were visualised on a 2% agarose gel and PCR product sizes estimated by comparing fragment sizes with a 100 bp DNA ladder (Promega, Wisconsin, USA). Products of the expected size were purified using a Roche High Pure PCR Purification Kit (Roche Diagnostics, Australia) and sequenced.

e. DNA sequence analysis

Sequence analysis of purified PCR products was performed using the BigDye (R) Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA) according to the manufacturer's instructions. Reactions were analysed on an Applied Biosystems 3730S Genetic Analyzer (Applied Biosystems). Sequence data were edited using Bionumerics v4.0 (Applied Maths BVBA, Ghent, Belgium) and then compared with those derived from an M. ulcerans isolate, cultured from a human patient from Point Lonsdale.

f. Whole genome sequencing and assembly

Genomic DNA was prepared from a possum M. ulcerans isolate (JKD8170) and a human M. ulcerans isolate (JKD8049), both from Point Lonsdale. Whole genome sequencing was performed using an Illumina Genome Analyzer II with 36 cycle paired-end chemistry. Reads were mapped to the reference strain M. ulcerans Agy99 (GenBank accession CP000325) using SHRiMP [30]. Single nucleotide polymorphisms (SNPs) and micro-indels (DIPs) were detected using Nesoni, a software tool for analysing high-throughput DNA sequence data (used in [31]). Nesoni tallied the raw base counts at each mapped position in each of the reference strains, and then compared them using Fisher's Exact Test to find variable nucleotide positions in JKD8170 relative to JKD8049. To exclude the possibility that additional mutations in JKD8049 may have occurred in regions not present in the reference M. ulcerans Agy99, de novo assembly of JKD8170 and JKD8049 was performed using Velvet [32] and the above SNP/DIP detection procedure was repeated using the resulting contigs as reciprocal reference sequences. The read data for JKD8170 and JKD8049 have been deposited in the NCBI Sequence Read Archive (SRA) as part of Study accession number SRP001289.

Culture of M. ulcerans

a. Culture of M. ulcerans from environmental samples

Culture of M. ulcerans from possum faeces was attempted by homogenising samples in bead bottles with Ringer's solution, decontaminating with an equal volume of 4% sodium hydroxide, incubating at room temperature for 15 mins and neutralising with 10% orthophosphoric acid (modified Petroff method). Samples were centrifuged at 4000 rpm for 20 mins and pellets resuspended in 2 ml Ringer's solution. 400 µl of the decontaminated suspension was used to inoculate Mycobacteria Growth Indicator Tube (MGIT) broths with PANTA added according to the manufacturer's recommendations (BD, Franklin Lakes, N.J.), Brown and Buckle slopes and 7H10 slopes with antibiotics (25 µg/ml piperacillin, 50 µg/ml amphotericin, 25 µg/ml vancomycin, 800 µg/ml actidione, 4 µg/ml aztreonam). MGIT broths and solid media were incubated at 31°C and monitored weekly for up to 16 weeks.

b. Culture of M. ulcerans from possum lesions

Swabs were placed in bead bottles with 2 ml phosphate buffered saline (PBS), vortexed, decontaminated with 2% sodium hydroxide, incubated at room temperature for 15 mins and neutralised with 10% orthophosphoric acid. Samples were then centrifuged at 4000 rpm for 20 mins and pellets resuspended in 2 ml Ringer's solution. 400 µl was used to inoculate Brown and Buckle slopes and MGIT broths with PANTA added according to the manufacturer's recommendations (BD, Franklin Lakes, N.J.) and were incubated at 31°C with weekly monitoring for up to 12 weeks.

Human case definition and BU incidence

A case of BU was defined as a human patient with a suggestive clinical lesion from which M. ulcerans was identified by PCR [26] or culture from January 2005 to December 2009 inclusive. The likely geographic origin of infection was determined on the basis of the patient's residential address and/or travel history. A patient was considered as having acquired BU from a particular geographic area if he/she was a resident of, or a visitor to, that area and had not reported recent contact with any other known BU endemic area. Due to the large seasonal fluctuations in the population of endemic areas (most of which are summer holiday destinations), and the difficulty in estimating the number of visitors to a particular area, the average annual incidence of BU in each geographic area over the five-year study period was calculated by dividing the average annual number of cases in residents only (that is, cases in visitors were excluded) by the resident population of the specified geographic area. Resident population numbers were obtained using Australian Bureau of Statistics data derived from the 2006 Census of Population and Housing [33].

Statistical analyses

Statistical analyses were performed using STATA version 10.0 (STATA Corporation, College Station, TX). Proportions were compared using the two-sample test of proportion.


Environmental testing in Point Lonsdale and areas of low BU endemicity

Testing of environmental samples commenced in mid-2004, just prior to the peak of the Point Lonsdale outbreak. The initial focus was low-lying, wet areas in which mosquitoes were likely to breed, such as drains, soak pits (covered concrete pits into which storm water and street runoff flows and sits until it gradually seeps into the ground), man-made lakes and natural water bodies. In Point Lonsdale, low levels of M. ulcerans DNA (that is, weak positive real-time PCR signals for IS2404, IS2606 and KR) were detected in sediment from a man-made lake; soil, sediment and detritus from a number of different soak pits and drains; biofilm; aquatic plants; and residue from filtered water (Table 1). The estimated bacterial loads for these samples ranged from 10–100 organisms/ml for residue from filtered water and 103–104 organisms/gram for biofilm. In contrast, only four samples (two soil and two vegetation) from low endemicity areas were positive for M. ulcerans DNA (Table 1).

In late 2006, the scope of our environmental testing expanded to samples in dryer areas at higher elevations, including leaf litter, leaves, tree bark, flowers, seeds, stems and faeces from brushtail possums (Table 1). The rationale for this was: (i) soil collected outside drains had previously tested positive for M. ulcerans DNA, (ii) BU patients have reported an association between small penetrating injuries, sustained from vegetation, and subsequent ulcers [34], and (iii) cases of BU are known to occur in arboreal marsupial mammals, including koalas [7] and ringtail possums [8]. Testing revealed that while M. ulcerans DNA could be detected at low levels in some samples of leaf litter and bark from trees (estimated bacterial load 102–103 organisms/gram), much higher levels of M. ulcerans DNA were detected in brushtail possum faeces (estimated bacterial load ≥106 organisms/gram). This important discovery led to the large scale, systematic testing of possum faeces in Point Lonsdale, as well as low and non-endemic sites.

Possum faecal testing in BU high-, low- and non-endemic sites

Over a two-year period (2007–09), systematic collection of faeces from brushtail and ringtail possums was carried out across Point Lonsdale, nearby low endemicity areas and non-endemic areas (Table 2). A total of 589 faecal samples from ringtail possums and 250 samples from brushtail possums were tested. The difference in the number of samples collected from each geographic location and from each species reflected the relative population densities, with ringtail possums being much more abundant than brushtail possums in many areas sampled (K. Handasyde and A. Legione, unpublished data).

In Point Lonsdale, M. ulcerans DNA (IS2404) was detected in 43% of ringtail possum and 29% of brushtail possum faecal samples (Table 2). All samples tested for the presence of IS2606 and KR were PCR-positive for these additional targets. Furthermore, the ΔCt (IS2404-IS2606) was always in the range expected for M. ulcerans (2.17–2.79), rather than another MPM (6.94–8.07) [26]. The median estimated bacterial load was 104 organisms/gram (range: 102–108 organisms/gram) for ringtail possums (Fig. 3), with 17% of positive samples having an estimated bacterial load >106 organisms/gram. The median estimated bacterial load for brushtail possum faeces was 102–103 organisms/gram (range: 102–106 organisms/gram).

Figure 3
Distribution and estimated bacterial load of M. ulcerans-positive ringtail faecal samples in two towns.

In low endemicity areas, the proportion of PCR-positive faecal samples varied by location. For example, in Barwon Heads, where 15 human cases of BU have been reported since 2005, the proportion of positive ringtail and brushtail faecal samples was relatively high (26% and 19% respectively) compared with the other locations where fewer cases of BU have been reported (Table 2). The median estimated bacterial load of positive faecal samples from low endemicity areas also varied. In Barwon Heads the median estimated bacterial load for ringtail possum faeces was 104 organisms/gram (with 16% of the positive samples having an estimated bacterial load >106 organisms/gram). As in Point Lonsdale, the estimated bacterial load of the positive brushtail possum faeces in Barwon Heads was generally lower than for the ringtail possum faeces, with a median estimate of 102–103 organisms/gram. Similarly low M. ulcerans bacterial loads of 102–103 organisms/gram were estimated for faeces (ringtail possum only) collected in Queenscliff [Fig. 3] and Phillip Island. Only one sample collected from a non-endemic area (Torquay) was positive for M. ulcerans DNA and the estimated bacterial load of this sample was low (102–103 organisms/gram).

Mapping of the samples collected in Point Lonsdale revealed that M. ulcerans DNA could be detected throughout Point Lonsdale and did not appear to be concentrated in one particular area or limited to one particular point source (Fig. 3). However, in Barwon Heads, positive faecal samples were only detected in the southern part of the town (data not shown). No seasonal trends were observed, with the number of positive samples, and the estimated bacterial loads of those samples, consistent between summer, autumn, winter and spring (data not shown).

All attempts at culturing M. ulcerans from possum faeces were unsuccessful. PCR-positive and PCR-negative possum faeces were inoculated into MGIT and onto Brown and Buckle and 7H10 slopes with antibiotics. The MGIT broths and Brown and Buckle slopes exhibited extensive fungal contamination after two weeks and were discarded. Despite the absence of fungal contamination on the 7H10 slopes, no growth of M. ulcerans was detected after 16 weeks incubation.

Capture and examination of possums from Point Lonsdale

Over a 20-month period from February 2008 to November 2009, 42 ringtail possums and 21 brushtail possums were captured in Point Lonsdale and examined for BU disease. Among the ringtail possum cohort, 16 (38%) animals had laboratory-confirmed (PCR ± culture) M. ulcerans lesions and/or M. ulcerans PCR-positive faeces. Of the 11 animals with BU disease, nine had M. ulcerans PCR-positive faeces, one had M. ulcerans PCR-negative faeces and we were unsuccessful in collecting a faecal sample from the remaining animal (Table 3). Notably, five of the ringtail possums that did not have BU skin lesions had M. ulcerans PCR-positive faeces. Interestingly, as shown in Table 3, there was little difference in the median estimated bacterial loads of faeces from animals with BU skin lesions and animals without BU lesions. The incidence of M. ulcerans infection among the 21 brushtail possums was lower. One animal had a BU skin lesion and M. ulcerans PCR-positive faeces (estimated bacterial load, 103–104 organisms/gram) and four animals without BU lesions were found to be shedding low levels of M. ulcerans DNA in their faeces (102 organisms/gram) (Table 3).

Table 3
Mycobacterium ulcerans status of ringtail and brushtail possums captured in Point Lonsdale, Victoria, and examined for BU lesions and the presence of M. ulcerans DNA in faeces.

The most common site for BU lesions was the tail (Fig. 2E). Amongst the 12 possums with BU disease, nine had lesions on the tail and four had lesions on the toe/foot (Table 4). Five of the ringtail possums had multiple lesions, with one animal having severe ulcerative and oedematous lesions on her nose (Fig. 2F), left upper lip, both fore paws, right hock, left hind leg and tail. Three of these animals were euthanased and full necropsies performed to determine the extent of the M. ulcerans infection. The results of these necropsies, along with the results of the other clinical samples taken from all 63 possums captured (including blood, buccal swabs and nasal swabs and urine), are described in a separate report (manuscript in preparation).

Table 4
Characteristics of possums with laboratory-confirmed BU lesions captured in Point Lonsdale, Victoria, 2008–09.

VNTR/MIRU typing of possum faecal samples demonstrates identity with human outbreak strain

The two multiplex real-time PCR assays used in this study to detect M. ulcerans in environmental samples distinguish between M. ulcerans and other MPM that also harbour IS2404 and IS2606 [26]. However, we also sought to determine whether the DNA detected in environmental samples was from the same strain of M. ulcerans that causes disease in humans in Victoria. PCR reactions for 10 VNTR loci and three MIRU loci were performed on a subset of DNA extracts from possum faeces (estimated bacterial load 105–106 organisms/gram), aquatic plant biofilm (estimated bacterial load 103–104 organisms/gram) and water filters (estimated bacterial load 103–104 organisms/filter). The concentration of M. ulcerans DNA in the other sample types (for example, soil) has previously been shown to be insufficient for PCR amplification of these single copy loci [35]. DNA extracted from the possum faeces generated PCR amplicons of the same size (Fig. 4) and sequence as the Victorian human outbreak strain at all loci. As predicted by the lower concentration of M. ulcerans DNA in the samples, DNA extracts from the aquatic plant biofilm and water filter generated PCR amplicons at one locus only (VNTR locus 6 and 19, respectively). In each case the sequence was identical to the Victorian outbreak strain. These data provide evidence that the strain of M. ulcerans detected in these samples is the same as the strain which causes disease in humans in this region. The results also confirm that this method of analysis can only be applied successfully to samples (clinical or environmental) with an estimated M. ulcerans load of ≥105 organisms/gram and should only be used as a confirmatory/epidemiological tool and not as the primary method by which all environmental samples are screened for the presence of M. ulcerans DNA [35].

Figure 4
Variable number tandem repeat (VNTR) typing of M. ulcerans DNA in possum faeces demonstrates identity with human outbreak strain.

Whole genome sequencing of an M. ulcerans isolate from a ringtail possum

Illumina high-throughput short-read sequencing was used to compare the genome of an M. ulcerans isolate from a ringtail possum captured in Point Lonsdale (M. ulcerans JKD8170) and a human clinical isolate from Point Lonsdale (M. ulcerans JKD8049) obtained during the period of the M. ulcerans outbreak. This process generated 31,028,581 reads for JKD8170 and 10,921,914 reads for JKD8049. Bioinformatic analysis involved read mapping to the reference genome M. ulcerans Agy99 and reciprocal comparisons to consensus sequences derived from de novo sequence assemblies of each data set. These analyses revealed that both the possum and human isolates shared 5455 SNP differences compared to the reference genome (an African strain) but were differentiated from each other by only two SNPs (confirmed by PCR and Sanger DNA sequencing) across 5.6 Mb of chromosomal DNA sequence. These data confirm the extremely close genetic relationship between the human and possum isolates.


Elucidation of the mode of transmission and environmental reservoir(s) of M. ulcerans is essential for the development of strategies to control and prevent BU outbreaks. Early epidemiological studies from Uganda in the 1970s suggested that M. ulcerans may be associated with certain grasses growing at the edges of permanent swamps [36], [37], and that transmission to humans was via contact with this environmental source. However, attempts to culture M. ulcerans from a range of plants were unsuccessful [38]. The possible role of rodents in the ecology of M. ulcerans was also considered over 30 years ago [39], however the presence of the organism in the organs of 700 animals from a BU endemic area in Uganda could not be confirmed by culture. The development of IS2404 PCR in the 1990s [16], [40] enabled researchers to detect the DNA of M. ulcerans and other MPM in a range of different samples, leading to a renewed search for the environmental reservoir(s). The PCR detection of M. ulcerans DNA in waterbugs from Benin and Ghana [18] and subsequent culture of M. ulcerans from a waterbug [14], focussed the search to aquatic habitats. Currently, the prevailing dogma is that the environmental reservoir of M. ulcerans is an abiotic or biotic component of aquatic, rather than terrestrial, ecosystems. Indeed, numerous epidemiological and environmental studies support this view [5], [11], [12], [14], [15], [17][21], [26], [41][43], including some of the data from our current study. We found that M. ulcerans could be detected in various aquatic samples including aquatic plants, biofilm and residue from filtered water (Table 1). The major strength of our study, however, was the use of a suite of real-time PCR assays targeting multiple regions in the M. ulcerans genome which, in addition to being highly sensitive, specific and less prone to contamination than conventional gel-based PCR [12], [13], enabled us to estimate the relative numbers of M. ulcerans in the various samples tested by determining the relative concentrations of M. ulcerans DNA among the different sample types.

By following this gradient of M. ulcerans DNA, we discovered that the faeces of two marsupial mammals (ringtail and brushtail possums), contained higher concentrations of M. ulcerans DNA than the other samples tested. The large-scale testing of possum faeces in BU high-, low- and non-endemic sites, and the subsequent capture and examination of possums in Point Lonsdale, generated a number of important findings. Firstly, we discovered that there is a high density of ringtail possums throughout Point Lonsdale that are excreting copious amounts of faeces, almost half of which are estimated to contain M. ulcerans, into the environment (Table 2, Fig. 3). Secondly, we observed a strong positive correlation between the BU endemicity of an area and the proportion and DNA concentration of M. ulcerans-positive possum faeces, with 41% of faecal samples collected in Point Lonsdale testing positive for M. ulcerans compared with less than 1% of faecal samples collected from non-endemic areas (p<0.0001). Similar results were obtained in Benin with a correlation between BU endemicity in patients and environmental results. Environmental studies detected variations in M. ulcerans DNA positivity rates of aquatic insects over time, and these changes were reflected in corresponding alterations of frequency of BU patients in the same foci [44]. Thirdly, 38% of captured ringtail possums and 24% of captured brushtail possums were found to have laboratory-confirmed M. ulcerans skin lesions, mostly on the tail or feet, and/or M. ulcerans PCR positive faeces (Table 3). One explanation for the observation that most lesions occurred on the extremities is that these sites have lower temperatures favouring the growth of M. ulcerans. Another possibility is that, because these sites have less fur, they are more susceptible to insect bites or skin trauma via contact with vegetation or fighting with other possums, which may lead to inoculation of M. ulcerans. Fourthly, we observed that five of the 14 ringtail possums, and four of the five brushtail possums, that were shedding M. ulcerans DNA in their faeces did not have BU skin lesions, indicating that the presence of M. ulcerans DNA in faeces is not limited to clinically diseased animals (Table 3). However, we noted that animals with multiple lesions tended to have higher estimated faecal loads of M. ulcerans than animals with single lesions (data not shown). Finally, whole genome sequencing confirmed the extremely close genetic relationship between the human and possum isolates.

Taken together, these findings suggest that possums may be an environmental reservoir for M. ulcerans in south-eastern Australia. If so, the biology of possums prompts a new interpretation/understanding of the life cycle of M. ulcerans. In particular, ringtail possums are exclusively arboreal, feeding on a variety of leaves of both native and introduced plants, as well as flowers and fruits [45], hence are unlikely to be exposed to M. ulcerans in soil or water. They are also caecotrophic. Caecotrophy is the ingestion of soft faeces of high nutritive value derived from caecal contents and is a critical factor in the ringtail possum's ability to utilise eucalypt foliage as a whole or major food source [46]. This behaviour may also favour gastrointestinal persistence of M. ulcerans. Brushtail possums are semi-arboreal, spending a considerable portion of their foraging time on the ground and, although mainly folivorous, have a more varied diet than ringtail possums [45]. The ecology of these species, which occur in strictly terrestrial habitats, contradicts the idea that the environmental host(s) of M. ulcerans are likely to reside primarily in aquatic environments, although the presence of M. ulcerans in aquatic habitats within the same location is also likely, based on data presented in this study. Thus, in light of our data, we suggest that reservoir species could include terrestrial mammals, and that the association of the disease with low-lying, wetter areas might be driven by the dependence of a vector species (such as mosquitoes [47]) on moist habitats.

A disease reservoir may be defined as: “one or more epidemiologically connected populations or environments in which a pathogen can be permanently maintained and from which infection can be transmitted to the target population. Populations in a reservoir may be the same or a different species as the target and may include vector species” [48]. Our findings from Point Lonsdale suggest that at least one free-ranging mammal species (the ringtail possum), which can be very abundant in urban environments, forms part of a transmission cycle (Fig. 5) for M. ulcerans that could explain human outbreaks of BU in south-eastern Australia, although they may not necessarily be true maintenance hosts (that is, be able to maintain the organism in the absence of other environmental sources). However, bovine tuberculosis, caused by Mycobacterium bovis, and Johne's disease, caused by Mycobacterium avium subsp. paratuberculosis, are both maintained in wildlife reservoir species. In the United Kingdom, badgers (Meles meles) contribute to the spread of M. bovis between herds of cattle [49]. In New Zealand, where bovine tuberculosis is a major problem, the principle wildlife host for M. bovis is the common brushtail possum, which was originally imported from Australia and now occurs at such a high population density that it is a major agricultural and conservation pest [49].

Figure 5
Proposed transmission pathways of M. ulcerans between the environment, mosquitoes, possums and humans.

The way in which M. ulcerans might be transmitted from an animal to humans is not clear. A similar epidemiology to leptospirosis, the most common zoonosis worldwide [50], in which rodents are reservoirs but the disease is acquired by contact with contaminated water, should be considered. We envisage that the transmission pathway for M. ulcerans may involve vegetation, vertebrate hosts and invertebrate vectors in both terrestrial and aquatic ecosystems (Fig. 5). Such a model represents a fundamental change to the existing views on the ecology of M. ulcerans, although the idea that M. ulcerans is not confined to low-lying swampy areas is not new [36][39], [51], [52]. While we lack important information about whether mosquitoes are productive or simply mechanical vectors, and have only limited information on the site of carriage/colonisation, either on or within mosquitoes, a number of lines of evidence implicate mosquitoes as vectors of M. ulcerans in Victoria [6], [53][55]. Given that we found active M. ulcerans lesions in 26% of captured ringtail possums, transmission to humans might occur when an adult mosquito that has fed on a diseased possum, or rested on vegetation contaminated by a possum lesion, subsequently bites a human. Another possibility is that heavy environmental contamination with possum faeces containing M. ulcerans would enable mosquitoes (either as larvae or adults) to come into contact with M. ulcerans, in contaminated soil/water in roof gutters or drains (Fig. 5). This is supported by a study by Tobias et al. which showed that, in a feeding experiment where mosquito larvae were fed possum faecal material spiked with M. ulcerans or M. marinum, M. ulcerans accumulated within the mouth and midgut whereas M. marinum did not [55].

Key to determining which of these potential routes of transmission is most likely (or possible) is the demonstration of viable M. ulcerans organisms in possum faeces. We acknowledge that the detection of M. ulcerans DNA in possum faeces does not necessarily indicate the presence of viable organisms. However we, like many others who have attempted to culture M. ulcerans from environmental samples [14], have currently been unable to culture M. ulcerans from possum faeces. This was despite the fact that some of the samples had real-time PCR signals equivalent to those obtained for the lesion swabs from which culture of M. ulcerans was successful (data not shown). We believe that this has been largely due to the presence of fungi or fungal spores in the faecal samples which, despite decontamination methods, rapidly grew in broth cultures and on Brown and Buckle slopes and inhibited the growth of slower growing organisms such as M. ulcerans. Furthermore, on the basis of subsequent real-time PCR studies, it has become evident that the organisms are tightly associated with the particulate matter and that homogenising faeces in bead bottles results in very few bacteria in the suspension that would normally be used to inoculate the culture media (C. O'Brien, unpublished). We have also found that intact DNA can be recovered from possum faeces many months after sampling and that DNase treatment of the faecal homogenate does not lead to a reduction in the PCR signal (data not shown). This suggests that intact M. ulcerans organisms are present (though not necessarily viable), rather than just free M. ulcerans DNA.

There is also the question of whether mammals could act as reservoirs in sub-Saharan Africa, where the majority of BU cases occur. Recent studies in Ghana failed to detect M. ulcerans in the organs or faeces of rodents and shrews [17], [56]. However these authors did not reject the hypothesis that these, or other species of small terrestrial mammals, may be part of the reservoir of M. ulcerans in this setting. Recent work conducted by our group, including the post-mortem examination of ringtail possums and rats (Rattus rattus) with and without clinical BU disease, has shown that M. ulcerans can be present in the gastrointestinal tracts of animals but not in the organs of the same individual (manuscript in preparation). We are currently investigating the potential role of other mammal species as hosts for M. ulcerans in the Australian setting.

This study has led to a major a shift in our understanding of the environmental distribution of M. ulcerans in south-eastern Australia. It is hoped that the results presented here, along with our continuing laboratory and field research, will take us closer to elucidating the mode of transmission and environmental reservoir(s) of M. ulcerans and in turn the development of strategies to control and prevent this important yet often neglected human disease.


We thank the laboratory staff of the Mycobacterium Reference Laboratory at VIDRL for their technical advice and James Fielding and Dallas Wilson of VIDRL for assisting with statistical analyses and preparation of figures, respectively. We are grateful to Joseph Azuolas and Karen Browne of the Victorian Department of Primary Industries for assistance with field work and the Department of Primary Industries for the use of its mobile DNA extraction vehicle. We thank Neville Walsh of the Royal Botanic Gardens, Melbourne, for collecting and identifying terrestrial plant specimens and Koen Vandelannoote (Institute of Tropical Medicine, Antwerp) and Theresa Ruf (Swiss Tropical and Public Health Institute, Basel) for assisting with the collection and testing of environmental samples.


The authors have declared that no competing interests exist.

This research was predominantly funded by the State of Victoria through its Department of Health (Public Health Research Grants 2004-10). The views and conclusions are those of the authors and do not necessarily represent those of the Department of Health. The research was also supported in part by the Stop Buruli initiative funded by the UBS Optimus Foundation ( and the National Health and Medical Research Council of Australia. M. E. Benbow and J. R. Wallace were supported in part by grant number R01TW007550 from the Fogarty International Center through the National Institutes of Health/National Science Foundation (NIH/NSF) Ecology of Infectious Diseases Program, and grant number R03AI062719. Carolyn O'Brien is supported by an Australian Postgraduate Award. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


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