Buruli ulcer (BU) is a skin disease caused by Mycobacterium ulcerans, with endemicity predominantly in sub-Saharan Africa and south-eastern Australia. The mode of transmission and the environmental reservoir(s) of the bacterium and remain elusive. Real-time PCR investigations have detected M. ulcerans DNA in a variety of Australian environmental samples, including the faeces of native possums with and without clinical evidence of infection. This report seeks to expand on previously published findings by the authors' investigative group with regards to clinical and subclinical disease in selected wild possum species in BU-endemic areas of Victoria, Australia.
Twenty-seven clinical cases of M. ulcerans infection in free-ranging possums from southeastern Australia were identified retrospectively and prospectively between 1998–2011. Common ringtail possums (Pseudocheirus peregrinus), a common brushtail possum (Trichosurus vulpecula) and a mountain brushtail possum (Trichosurus cunninghami) were included in the clinically affected cohort. Most clinically apparent cases were adults with solitary or multiple ulcerative cutaneous lesions, generally confined to the face, limbs and/or tail. The disease was minor and self-limiting in the case of both Trichosurus spp. possums. In contrast, many of the common ringtail possums had cutaneous disease involving disparate anatomical sites, and in four cases there was evidence of systemic disease at post mortem examination. Where tested using real-time PCR targeted at IS2404, animals typically had significant levels of M. ulcerans DNA throughout the gut and/or faeces. A further 12 possums without cutaneous lesions were found to have PCR-positive gut contents and/or faeces (subclinical cases), and in one of these the organism was cultured from liver tissue. Comparisons were made between clinically and subclinically affected possums, and 61 PCR-negative, non-affected individuals, with regards to disease category and the categorical variables of species (common ringtail possums v others) and sex. Animals with clinical lesions were significantly more likely to be male common ringtail possums.
There is significant disease burden in common ringtail possums (especially males) in some areas of Victoria endemic for M. ulcerans disease. The natural history of the disease generally remains unknown, however it appears that some mildly affected common brushtail and mountain brushtail possums can spontaneously overcome the infection, whereas some severely affected animals, especially common ringtail possums, may become systemically, and potentially fatally affected. Subclinical gut carriage of M. ulcerans DNA in possums is quite common and in some common brushtail and mountain brushtail possums this is transient. Further work is required to determine whether M. ulcerans infection poses a potential threat to possum populations, and whether these animals are acting as environmental reservoirs in certain geographical areas.
Mycobacterium ulcerans causes skin disease predominantly in sub-Saharan Africa and southeastern Australia. The mode of transmission and the environmental reservoir(s) of the bacterium are unknown. Investigations have detected M. ulcerans DNA in a variety of Australian environmental samples, including the faeces of native possums. This report expands on these studies by detailing the clinical, pathological and microbiological findings in affected wild possum species in endemic areas. Twenty-seven clinically and 12 subclinically affected individuals were identified. Most clinical cases were adults with skin ulcers of the face, limbs and/or tail. The disease was mild and self-limiting in both Trichosurus spp. possums. In contrast, many of the common ringtail possums had multiple skin ulcers and in some there was evidence of internal disease. There were also significant levels of M. ulcerans DNA throughout the gut. Comparisons were made with regards to disease category, species and sex; with clinical cases more likely to be male common ringtail possums. Asymptomatic gut carriage of M. ulcerans DNA is quite common and may be transient in some individuals. Further work is needed to determine whether M. ulcerans infection poses a potential threat to possum populations, and whether these animals are acting as reservoirs in some areas.
Citation: O'Brien CR, Handasyde KA, Hibble J, Lavender CJ, Legione AR, McCowan C, et al. (2014) Clinical, Microbiological and Pathological Findings of Mycobacterium ulcerans Infection in Three Australian Possum Species. PLoS Negl Trop Dis 8(1): e2666. https://doi.org/10.1371/journal.pntd.0002666
Editor: Christian Johnson, Fondation Raoul Follereau, France
Received: August 6, 2013; Accepted: December 12, 2013; Published: January 30, 2014
Copyright: © 2014 O'Brien et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: CROB was supported by an Australian Postgraduate Award scholarship. This study was funded in part by The Department of Health, Victoria, via a Public Health Research Grant. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Mycobacterium ulcerans is an environmental organism that causes distinctive dermal lesions in people and animals, via the elaboration of the cytotoxic and immunosuppressive polyketide toxin, mycolactone . The disease is known internationally as Buruli Ulcer (BU). It has a worldwide but highly focal distribution, with endemicity recorded in 33 countries to date, predominately in sub-Saharan Africa and Australia. Sporadic cases and a number of localised outbreaks have been documented in people – and a variety of wild and domestic mammals – in southeastern Victoria, Australia, since the first reports of the disease over 60 years ago , .
Shortly after the initial reports of infection in people, it was shown that the common brushtail (CBT) possum (Trichosurus vulpecula, Kerr 1792) was experimentally susceptible to the disease , . These investigations were undertaken because this species was noted to be highly susceptible to infection caused by members of the M. tuberculosis complex . In brief, ulcerative lesions could be induced by local subcutaneous inoculation of organisms, and two animals inoculated via the intraperitoneal route developed lesions containing acid-fast bacilli (AFB) at peripheral sites (tail or tail base, scrotum, inguinal lymph node, stifle and front paw).
Despite this apparent susceptibility, there was no evidence of the infection in the wild CBT possum population in an endemic area of Victoria in the decades immediately following the initial outbreak, despite ongoing sporadic disease in the human population . However, following an outbreak of the disease in people on Phillip Island, Victoria in the mid 1990s, two local wild common ringtail (CRT) possums (Pseudocheirus peregrinus, Boddaert 1785) were confirmed with M. ulcerans infection .
Since 2000, there has been an ongoing outbreak of BU in residents and visitors to the Bellarine Peninsula of Victoria . Analysis of environmental samples using a highly sensitive real-time polymerase chain reaction (PCR) technique targeting sequences within IS2404, IS2606 and KR , ,  has confirmed low levels of M. ulcerans DNA in plant biofilms, vegetation, soil samples and local mosquitoes , and much higher levels (in some instances greater than 106 organisms/gram), in the faeces of local wild CRT and CBT possums . Despite this, the culture of viable organisms from these samples has remained elusive . Variable-number of tandem repeats (VNTR) profiles of the DNA extracted from Point Lonsdale possum faeces was indistinguishable from that of the Victorian human outbreak strain of M. ulcerans , . This report expands on the previous work performed by the authors' investigative group, by describing in detail the clinical, microbiological and pathological features of M. ulcerans infection of 27 clinical and 12 subclinical possum cases domiciled in three endemic areas of southern Victoria, Australia: Cowes (Phillip Island), Bellbird Creek (East Gippsland) and Point Lonsdale (Bellarine peninsula). This report represents the largest case series of naturally occurring M. ulcerans infection in any non-human species to date. Possible links between the disease in people and the resident possum population, and future avenues of investigation are discussed.
Materials and Methods
‘Clinical’ cases were defined as any possum with ulcerative skin lesions from which M. ulcerans was cultured, or was detected by IS2404 PCR from clinical material, including swabs and necropsy tissues. ‘Subclinical’ cases were defined as any possum from which M. ulcerans was cultured or was detected by PCR from clinical material, including gut contents and/or faeces, where there was no gross or histopathological evidence of disease. During the course of the investigation, any possum in which no M. ulcerans DNA could be detected via PCR in any clinical sample was classified as ‘non-affected’.
Retrieval of cases
Cases were identified by a review of the record database of the Mycobacterium Reference Laboratory of the Victorian Infectious Diseases Reference Laboratory (VIDRL) from 1998 to 2011, and from prospective capture and sampling of possums indigenous to some known M. ulcerans-endemic areas of Victoria; Bellbird Creek, between 2007–2012, as part of a routine surveillance program conducted by the Department of Environment and Primary Industries, and Point Lonsdale between 2008–2010, as part of an epidemiological study of M. ulcerans disease in these species. The methods of the latter study have been published elsewhere . Clinical and/or autopsy data were also retrieved from case records of Newhaven Veterinary Clinic, Phillip Island, Victoria, the veterinary department of Melbourne Zoo, Parkville, Victoria, the laboratory records of the University of Melbourne Veterinary Hospital, Werribee, Victoria and the Department of Environment and Primary Industries, Veterinary Diagnostic Services, Victoria. Where available, data such as species, sex, estimated age at diagnosis (juvenile/adult), year of diagnosis, geographical location of domicile, anatomical location and nature of lesions, and results of autopsy examination (including histopathology) were recorded. Fresh faeces from mountain brushtail (MBT) possums (Trichosurus cunnighami, Lindenmayer 1990) trapped at Bellbird Creek were collected from within or underneath traps. For some possums trapped in Point Lonsdale, one to two millilitres of blood was collected from the cephalic, medial saphenous, or tail vein and placed in a plain tube. The blood sample was centrifuged at 16,100 g (Eppendorf 5415D, Hamburg, Germany) for 2 minutes before the serum was separated and stored at −80°C, the pellet was used for IS2404 PCR analysis. Urine was collected via percutaneous cystocentesis where possible. Buccal and nasal swabs were obtained from some individuals. Fresh faeces were collected from underneath traps or from holding bags; a cloacal swab was collected from individuals if no faeces were obtained. Details of the methods utilised in the capture and sampling of possums has been described previously . The project was approved by the University of Melbourne Faculty of Veterinary Science Animal Experimentation Ethics Committee (project no. 0706769) and was carried out under a permit from the Victorian Department of Sustainability and Environment (DSE permit no. 10004406).
Apart from case 28, which was found deceased, animals that underwent autopsy examination were euthanased with an overdose of sodium pentobarbitone, and tissues collected were either fixed in 10% buffered formalin for histopathology or were submitted fresh for microbiology. Formalin-fixed tissues were then embedded into paraffin blocks and processed routinely prior to staining with haematoxylin-eosin and/or acid-fast staining with either Ziehl-Neelsen (ZN) stain or Wade's modification of the ZN stain .
Initially, IS2404 PCR was performed by the Microbiological Research Unit, Royal Children's Hospital (prior to 2002) and thence at VIDRL, utilising the methods published by Ross et al . Since 2003, a multiplex real-time PCR assay has been used to test clinical and environmental samples for the presence of M. ulcerans DNA .
Culture of M. ulcerans from lesions and necropsy tissue was carried out after decontamination via incubating at room temperature for 15 minutes with either 2 or 4% sodium hydroxide, followed by neutralisation with 10% orthophosphoric acid. The samples were then centrifuged at 3082 g (Beckman Coulter Allegra X-22, Pasadena, California, USA) for 20 minutes and the resultant pellet was re-suspended in 2 ml of Ringer's solution. 400 µl was then used to inoculate Brown and Buckle slopes, and Mycobacterium Growth Indicator Tubes (BD, Franklin Lakes, N. J.) admixed with 0.8 ml of manufacturer-supplied antibiotic mixture and incubated for up to 12 weeks at 31°C, with weekly or fortnightly monitoring by either visual inspection or IS2404 real-time PCR.
Isolates were typed by either restriction fragment length polymorphism (RFLP) typing , variable-number of tandem repeats (VNTR) typing ,  and in two instances, whole genome sequencing .
Numerous samples were collected from 69 possums.. Faecal samples were collected from 57 individual animals; in the first instance 14 (25%) of these samples were PCR-positive for M. ulcerans DNA. In six animals multiple faecal samples were collected over the course of the study; in three cases 2 of 2 samples were negative, in one case 2 of 2 were positive and in three cases 1 of 2, 1 of 5 and 1 of 6 samples were PCR-positive respectively. Blood samples were collected from 63 individuals, none of which were PCR-positive. Buccal swabs were obtained from 67 individuals; 7 (16%) were PCR-positive. Urine samples were collected from 16 animals; all were PCR-negative. Pouch swab samples were collected from 15 possums; 3 (20%) of which were weakly PCR-positive. Twenty cloacal swab samples were collected (often in lieu of a faecal sample); the one instance where this sample was PCR-positive, the animal was concurrently documented to have PCR-positive faeces.
Twenty-seven clinically affected animals were identified for inclusion in the study (Table 1). There were 23 CRT, one CBT and one MBT possum. For two possums, species was not recorded. Of the 25 animals for which sex was recorded 17 (69%) were male. Of the 24 animals in which an age estimate was performed, one was a juvenile and 23 were estimated to be adults (although more objective data such as dental examination were not utilised).
Thirteen of the animals (11 CRT possums and two species not recorded) were from the Cowes region of Phillip Island, Victoria (Figure 1). These animals had been surrendered to the local veterinary hospital (Newhaven Veterinary Clinic) because of illness or trauma between 1998 and 2011. The MBT possum was captured in 2005 at Bellbird Creek (Figure 1). This animal was transferred to Melbourne Zoo, Parkville, Victoria, for management. Thirteen animals (12 CRT and one CBT) were from Point Lonsdale, Victoria (Figure 1); all were trapped between 2008–2010 as part of the prospective epidemiological study.
The nature and anatomical location of lesions were recorded for 25 possums (Table 1). Twelve animals had single skin lesions, five had two skin lesions and eight animals had multiple skin lesions, involving three or more anatomical sites. Lesions recorded on CRT possums were located on the face and/or head (n = 13), feet and/or limbs (n = 11) and tail and/or tail base (n = 14) (Figure 2). One animal also had scrotal ulcers (as well as multiple lesions at other sites). One CRT fitted with a radio-tracking collar (case 26), noted to initially have a solitary tail lesion, was found deceased several months later with a large IS2404 PCR-positive lesion on the ventrolateral thorax. The CBT possum had a small ulcer on a front toe (Figure 3a) and the MBT had a single ulceration on the left hind foot (Figure 3b). Both of these animals were noted to have spontaneous healing of lesions without specific treatment over a 3–6 month period. Only CRT possums were recorded to have two or more lesions, with six disparate anatomical sites in two instances.
This animal had multiple affected sites characterised by ulceration and/or oedema. (Image C. McCowan/J. Fyfe).
This lesion later underwent spontaneous resolution. (Image H. McCracken).
Eight animals (cases 5, 8, 14–16, 24, 25, and 27) underwent partial or complete autopsy examination. The necrotic skin ulcers appeared grossly and histopathologically similar to those described in other species , , . The lesions were characterised by extensive loss of the epidermis. A superficial crust composed of serous exudate and degenerate leukocytes was present, overlying a necrotic base (Figure 4a). The margins of the lesions were characterised by proliferative epidermis overlying fibrotic and sometimes, oedematous dermal tissue admixed with pyogranulomatous and/or lymphoplasmacytic inflammation. In ZN-stained sections, abundant numbers of AFB were present in the dermis, either extra-cellularly, or within macrophages (Figure 4b).
The lesion is characterised by proliferative epidermis overlying fibrotic dermal tissue admixed with inflammatory cells, and superficial crust composed of serous exudate and degenerate leukocytes overlying a necrotic base. (H&E stain)) (b): Demonstration of numerous acid-fast bacilli (AFB) in an ulcerated skin lesion of case 16 (modified ZN stain), (c): the liver lesions in this case contained rare AFB, mostly within macrophages (arrow) (modified ZN stain). (Images C. McCowan).
Four animals with extensive cutaneous disease (cases 16, 24, 25 and 27) also had evidence of systemic involvement, with patchy granulomatous, neutrophilic and/or lymphoplasmacytic lesions in the liver and lung. Rare AFB were present in macrophages in some sections of liver (Figure 4c).
The results of the microbiological investigations for clinically affected animals performed on either lesion swabs and/or necropsy material and, in most cases, gut contents or faeces are presented in Tables 2 and 3. M. ulcerans was cultured from skin lesions only in 19 animals, the liver, spleen and a mandibular lymph node in case 19, and skin lesions, liver, lung and small intestinal contents in case 27. The organism was also cultured from the abdominal cavity of the decomposing carcass of case 26.
RFLP typing of isolates was performed in four cases and found to be “V1” type . VNTR typing was performed in 15 cases and was found to be indistinguishable from M. ulcerans strains causing human and animal disease in Victoria. Analyses of the whole genome sequences of the isolates from cases 10 and 16, which have been described previously , confirmed a close genetic relationship with M. ulcerans isolates from Victorian human patients.
The duodenum of case 16 also contained a large tapeworm (species not identified), which was PCR-negative, despite the moderate real-time PCR-positivity of the small-intestinal contents of this animal. PCR-positive fly larvae (species not identified) were also retrieved from the carcass of case 26, however M. ulcerans, could not be cultured successfully from these larvae.
Twelve animals met the criteria for classification as a subclinical case (Table 4). These were all adult animals, comprising one male and three female CBT possums, four female CRT possums, and one male and three female MBT possums. The animals were domiciled in Point Lonsdale (CBT and CRT possums), and Bellbird Creek (MBT possums). One animal (case 28) was identified by a Point Lonsdale resident, while the remainder were trapped as part of the aforementioned studies (cases 29–39). Some CBT and MBT possums were trapped multiple times; the time-line of results from PCR analysis on faecal samples from these animals is presented in Figure 5.
In the majority of these individuals the gut carriage of M. ulcerans DNA was demonstrated to be transient.
 → Two subclinical cases (cases 28 and 32) underwent autopsy examination. Case 28 had been seen at ground level during the late afternoon and had appeared unusually docile. The animal was found deceased the following day and its body was submitted to the veterinary pathology service of The University of Melbourne a few days later. Although there was significant tissue autolysis, and cause of death could not be determined, there were no cutaneous lesions consistent with M. ulcerans infection. Low levels of M. ulcerans DNA were detected by real-time PCR in tissue from the liver, spleen, lung and gut wall, as well as small and large bowel contents and faecal pellets retrieved from the rectum. M. ulcerans as also cultured from the liver tissue. The carcass also contained fly larvae (species not identified), which were also weakly IS2404 PCR-positive.
Case 32 was found to have IS2404 PCR-positive faeces and was euthanased and underwent autopsy as part of the epidemiological study. The animal had no gross or histopathological lesions. A moderate level of M. ulcerans DNA was detected in all gut compartments (Table 3), and salivary gland tissue was also weakly PCR-positive .
Of the 69 animals trapped in Point Lonsdale, 50 (72%) had no detectable M. ulcerans DNA (via IS2404 real-time PCR) in any clinical sample. This cohort comprised 13 male and 6 female CBT possums, and 13 male and 18 female CRT possums. Eleven (73%) MBT possums trapped at Bellbird Creek had PCR-negative faecal samples on all trapping occasions. This group of animals comprised 7 males and 4 females.
Comparison of clinically, sub-clinically and non-affected possums
Categorical variables of (i) case type (clinical, subclinical and non-affected) (ii) species (CRT possum and non-CRT possum), and (iii) sex (male and female) were compared using 2×2 contingency tables (raw data presented in Table 5).
A comparison of animals with (clinical) and without cutaneous lesions (subclinical and non-affected possums) was made; the former animals were more likely to be CRT possums, or male, although the latter variable did not reach significance. When the variables of sex and species were combined, male CRT possums were more likely to have clinical lesions than other animals (odds ratios, including 95% confidence intervals and P values are presented in Table 6).
When comparisons were made between animals with a PCR-positive sample (both clinical and subclinical cases) and those in which all clinical samples were PCR-negative (non-affected cases) (results presented in Table 7), individuals in the former group were more likely to be CRT possums. There was no sex predilection for PCR-positivity.
The mean IS2404 real-time PCR signal strength (CT) of approximately 100 mg of faeces collected from clinically (n = 10) and sub-clinically affected (n = 12) animals was calculated as 29.32 (SD ±5.43) and 33.54 (SD ±4.82), respectively (raw data not shown) (Figure S1). When the values were compared, the difference was not statistically significant (P = 0.075).
Although there are previous reports of M. ulcerans infection in possums , , this is the first study to examine the clinical, pathological and microbiological aspects of the disease in detail, and also represents the largest and most comprehensive case series of the disease in any non-human species. Affected possums have only been recorded from areas of known M. ulcerans endemicity in Victoria, Australia. This is true for all reports of the infection in non-human mammalian species, despite the fact that the disease has been reported in many disparate areas of the world. The reasons for this epidemiological discrepancy are currently unknown, but may be due to specific host or environmental factors (for example, the presence of particular insect vectors in a temperate climate), or genomic differences related to virulence or host specificity of the ‘Victorian’ strain of M. ulcerans, compared to strains found elsewhere. There has been some attempt to identify animal cases in endemic areas of Africa and other parts of Australia, however this research has not yet yielded any positive results (J. Fyfe, C. Lavender, PDR. Johnson unpublished observations) , .
It has been reported that some species of marsupials appear prone to particular mycobacterial diseases  (for example, CBT possums and M. bovis infection, macropods and infections caused by the M. avium complex) and it is noteworthy that the next animal species most commonly reported with M. ulcerans infection is another Australian arboreal marsupial, the koala –. The prevalence of M. ulcerans infection in the possum populations in this study cannot be accurately estimated due to the inherent difficulties in sampling from a wild population; however, it appears that CRT possums are significantly more susceptible to clinical M. ulcerans infection than other possum species. Male CRT possums appeared to be particularly predisposed to clinical lesions, perhaps due to behaviours such as fighting (which was touted as a possible reason why male koalas appeared over-represented in an earlier study ) or as a result of stress associated with competition for territories. More extensive trapping and sampling and/or captive studies would be informative in revealing whether CRT possums have higher susceptibility to infection and disease across all BU-endemic areas in Victoria. Further, it is noteworthy that only CRT possums were observed with advanced clinical disease, with a number of animals displaying multiple lesions at disparate anatomical sites, and that some cases progressed to systemic disease involving the liver and lungs.
It is unclear whether the apparent susceptibility of the CRT possum is a function of impaired immunity or epidemiological factors such as high rates of environmental exposure, perhaps via communal sharing of contaminated dens (CRT possums are more social than most other possum species ), inoculation of the bacterium via penetrative wounds or insect vectors, or possibly via the practice of auto and/or allocoprophagy . Due to the economic impact of CBT possums as reservoirs for M. bovis in New Zealand, much effort has been expended in assessing the immunobiology of this species. No such data exist for the CRT possum and testing of the immunological competence of non-infected controls is needed to establish whether there are any inherent immunological deficiencies in these populations, and would be helpful in differentiating any local or systemic immunosuppressive effects of mycolactone in infected individuals.
The significance of variable levels of M. ulcerans DNA in the gastrointestinal tract of both clinically and subclinically affected possums in endemic areas is unknown. There were no lesions consistent with established gastrointestinal infection in any animals where histopathological examination of the gut was performed. The question as to whether these are viable organisms (and therefore represent a significant source of potentially infective organisms to other animals and people) remains unanswered, despite concerted attempts to culture M. ulcerans from fresh and aged PCR-positive faecal material collected from the environment, and fresh gut contents collected at autopsy. A single isolate was recovered from the small intestinal contents of a systemically affected CRT possum from Phillip Island, however the possibility of cross-contamination from lesions cannot be ruled out in this instance. Alternative methods to demonstrate metabolic activity of M. ulcerans within possum gut contents/faeces, for example, via rRNA or mycolactone detection remain a possibility, although negative findings may theoretically result if the organisms have become metabolically dormant.
Based on real-time PCR signal strength, there is no evidence that the organism is amplified in any particular region of the gut of affected animals. Nor does it appear that clinically affected cases have significantly greater amounts of M. ulcerans DNA in the gut compared to subclinical cases. There is also no sex predilection for PCR-positivity in the gut contents or faeces, perhaps suggesting a common environmental source of oral inoculation in all animals (even though there may be separate risk factors for clinical disease between the sexes).
If the organisms are viable within the gut, the daily practice of autocoprophagy in CRT possums  provides a possible route for re-inoculation and amplification of organisms in the gut of an individual (and thus ongoing colonisation/infection). It is not known whether this represents a source of horizontal transmission to other individuals (thus maintaining colonisation/infection in the population) via allocoprophagy. This seems most likely, perhaps, in juveniles approaching weaning. In the koala, which like the CRT is also a specialist folivore, establishment of normal gut flora in dependent juveniles occurs during weaning via allocoprophagy . An alternative significant environmental source of oral inoculation (for example, a contaminated food source) remains elusive, although interrogation of a variety of plant species (potentially foraged by CRT possums in some endemic areas) via IS2404 real-time PCR demonstrated low levels of M. ulcerans DNA (data not shown). Except in one instance, only animals with cutaneous lesions were found to have PCR-positive buccal swabs, which might suggest that the positivity of these samples may be due to contamination of the oral cavity via licking of ulcers. However, it cannot be conclusively shown that these findings are not due to ingestion of M. ulcerans DNA from the environment or contaminated caecotrophs.
The fact that the non-coprophagous CBT has also been noted to have similar levels of M. ulcerans DNA in the faeces  also argues for a potential oral environmental source. It is unknown at this stage whether the finding of M. ulcerans DNA in the gut of possums represents transient or persistent gut contamination, colonisation or infection, although in two CBT and four MBT possums trapped repeatedly over the course of the study low level faecal PCR-positivity was observed to be transient. The possibility that the M. ulcerans DNA was derived from soil or environmental detritus contamination of the external surface of the faeces was considered unlikely, given that the samples were mostly collected directly from within traps or collection boxes, rather than the ground. No record of whether gut PCR-positivity was transient or permanent in CRT possums was obtained due to the difficulties of repeat trapping of this species, even with the aide of radio-tracking collars (A. Legione, K Handasyde unpublished observations).
It is also not known whether gut colonisation/infection is directly linked with prior or eventual clinical disease. The only clinically affected individual without PCR-positive faeces (case 13) had numerous superficial cutaneous lesions on the tail that were different in appearance from the typically deep, undermined ulcers observed in other animals in the study. Whilst these lesions were weakly PCR-positive, it cannot be excluded that they were actually caused by a different disease entity (such as pox-virus infection ) that had become contaminated with M. ulcerans DNA from the environment.
Based on real-time PCR results of urine samples, it does not appear that M. ulcerans is shed via the urinary tract, nor is there evidence of mycobacteraemia in the animals from which blood samples were obtained. Thus, it is unlikely that possums are a significant source of potentially infective blood meals for vectors such as mosquitoes or flies, although mechanical transmission from the wounds of infected possums to humans via contaminated insect vectors cannot be ruled out.
While the natural history of this disease in possums is generally unknown, lesions were observed to undergo spontaneous remission in a CBT and a MBT possum in this study. It is not known if either of these two individuals eventually suffered disease relapse (one individual was kept in captivity but has been lost to follow-up, and one was released back into the wild). Due to the aforementioned difficulties in repeated trapping of CRT possums it is unknown whether clinical lesions are able to undergo spontaneous remission in this species. Given the state of ill-health of some of the CRT possums in this study, (and possibly the CBT possum, case 28) it seems that the disease may become progressive, possibly leading to death either directly due to the effects of the M. ulcerans infection, or due to secondary illness (although no co-morbidities were identified in severely affected animals that underwent autopsy). Unfortunately, in the two animals found deceased (cases 26 and 28) the cause of death could not be determined due to the state of decomposition, thus it is impossible to say what role, if any, M. ulcerans played in their demise.
The systemically affected CRT possums had histopathological evidence of disease in the lungs and liver. Lower respiratory tract infections have been previously reported in koalas with extensive nasal cavity disease, presumably due to inhalation of the organisms . The authors speculated that due to the organism's strict temperature requirements (27–33°C) the infection was possibly maintained in this anatomical site due to a sub-normal core body temperature that could occur in a moribund animal. Unfortunately, the core body temperature of the severely affected possums in this study was not measured, however the normal core body temperature of the CRT possum is 35–36°C , thus it is conceivable that these individuals may become sufficiently hypothermic to allow growth of M. ulcerans within the body . Circulating mycolactone has been detected in human patients , and may also play a role in producing systemic immunosuppression in animals with extensive disease.
Our initial study of M. ulcerans infection in possums has highlighted a number of areas that warrant further investigation. More detailed studies are necessary to document the natural history of the disease and the level of M. ulcerans DNA shed in the faeces over time, in both naturally and experimentally infected animals (especially CRT possums). One difficulty is that the stress of bringing wild possums into captivity is likely to confound results from any such investigations, and although ideally such aims could be achieved via radio-tracking of wild animals, the heavy attrition of CRT possums in their natural habitat , makes this work difficult, as a pilot study by our group has confirmed (A. Legione, K. Handasyde Unpublished observations). Research into the potential for horizontal and vertical transmission between possums is also needed, as well as ongoing attempts to determine the viability of M. ulcerans within gut contents/faeces.
In conclusion, the disease burden in CRT possums (especially males) in some areas of Victoria endemic for M. ulcerans disease appears significant. Whilst it appears that CBT and MBT possums with solitary cutaneous lesions have the ability to overcome the infection, the natural history of the disease generally remains unknown. In some instances, severely affected animals, especially CRT possums, may become systemically, and potentially fatally affected. As previous work has shown, subclinical gut carriage of M. ulcerans DNA in possums is quite common , and this study has shown that in some CBT and MBT possums it is transient. It is unknown whether this is also the case for CRT possums. Further work is required to establish whether this disease poses a potential threat to possum populations, and whether these animals are contributing to the high incidence of M. ulcerans infection in people in certain geographical areas by acting as environmental reservoirs.
Conceived and designed the experiments: CROB KAH PDRJ JAMF. Performed the experiments: CROB KAH ARL JH CJL MG CM ATM HEM PDRJ JAMF. Analyzed the data: CROB KAH PDRJ CJL JAMF. Contributed reagents/materials/analysis tools: CROB KAH ARL JH CJL MG CM ATM HEM PDRJ JAMF. Wrote the paper: CROB KAH PDRJ JAMF.
- 1. George KM, Chatterjee D, Gunawardana G, Welty D, Hayman J, et al. (1999) Mycolactone: a polyketide toxin from Mycobacterium ulcerans required for virulence. Science 283: 854–857.
- 2. Hayman JA, Huygens HJ (1982) Mycobacterium ulcerans infection across Lake Victoria. Med J Aust 1: 138.
- 3. Buckle G (1972) Notes on Mycobacterium ulcerans. Aust N Z J Surg 41: 320–323.
- 4. Anon (1975) Editorial: Mycobacterium ulcerans in Australia. Med J Aust 2: 660–661.
- 5. Radford AJ (1975) Mycobacterium ulcerans in Australia. Aust N Z J Med 5: 162–169.
- 6. Hayman J (1987) Mycobacterium ulcerans infection in Victoria: celebration of a golden jubilee? Australas J Dermatol 28: 99–105.
- 7. Hayman J (1991) Postulated epidemiology of Mycobacterium ulcerans infection. Int J Epidemiol 20: 1093–1098.
- 8. Hayman JA, Fleming HB, Monash DA, Miller IM (1991) Mycobacterium ulcerans infection in paradise. Med J Aust 155: 130.
- 9. Flood P, Street A, O'Brien P, Hayman J (1994) Mycobacterium ulcerans infection on Phillip Island, Victoria. Med J Aust 160: 160.
- 10. Goutzamanis JJ, Gilbert GL (1995) Mycobacterium ulcerans infection in Australian children: report of eight cases and review. Clin Infect Dis 21: 1186–1192.
- 11. Johnson PD, Veitch MG, Flood PE, Hayman JA (1995) Mycobacterium ulcerans infection on Phillip Island, Victoria. Med J Aust 162: 221–222.
- 12. Johnson PD, Veitch MG, Leslie DE, Flood PE, Hayman JA (1996) The emergence of Mycobacterium ulcerans infection near Melbourne. Med J Aust 164: 76–78.
- 13. Veitch MG, Johnson PD, Flood PE, Leslie DE, Street AC, et al. (1997) A large localized outbreak of Mycobacterium ulcerans infection on a temperate southern Australian island. Epidemiol Infect 119: 313–318.
- 14. Elsner L, Wayne J, O'Brien CR, McCowan C, Malik R, et al. (2008) Localised Mycobacterium ulcerans infection in a cat in Australia. J Feline Med Surg 10: 407–412.
- 15. Mitchell PJ, McOrist S, Bilney R (1987) Epidemiology of Mycobacterium ulcerans infection in koalas (Phascolarctos cinereus) on Raymond Island, southeastern Australia. J Wildl Dis 23: 386–390.
- 16. Mitchell PJ, Jerrett IV, Slee KJ (1984) Skin ulcers caused by Mycobacterium ulcerans in koalas near Bairnsdale, Australia. Pathology 16: 256–260.
- 17. McOrist S, Jerrett IV, Anderson M, Hayman J (1985) Cutaneous and respiratory tract infection with Mycobacterium ulcerans in two koalas (Phascolarctos cinereus). J Wildl Dis 21: 171–173.
- 18. Portaels F, Chemlal K, Elsen P, Johnson PD, Hayman JA, et al. (2001) Mycobacterium ulcerans in wild animals. Rev Sci Tech 20: 252–264.
- 19. Fyfe JA, Lavender CJ, Handasyde KA, Legione AR, O'Brien CR, et al. (2010) A major role for mammals in the ecology of Mycobacterium ulcerans. PLoS Negl Trop Dis 4: e791.
- 20. van Zyl A, Daniel J, Wayne J, McCowan C, Malik R, et al. (2010) Mycobacterium ulcerans infections in two horses in south-eastern Australia. Aust Vet J 88: 101–106.
- 21. O'Brien CR, McMillan E, Harris O, O'Brien DP, Lavender CJ, et al. (2011) Localised Mycobacterium ulcerans infection in four dogs. Aust Vet J 89: 506–510.
- 22. O'Brien CR, Kuseff G, McMillan E, McCowan C, Lavender C, et al. (2013) Mycobacerium ulcerans infection in two alpacas. Aust Vet J 91: 296–300.
- 23. MacCallum P, Tolhurst JC, Buckle G, A SH (1948) A new mycobacterial infection in man. J Pathol Bacteriol 60: 93–122.
- 24. Bolliger A, Forbes BRV, Kirkland WB (1950) Transmission of a recently isolated mycobacterium to phalangers (Tichosurus vulpecula). Aust J Sci 12: 146–147.
- 25. Forbes BR, Wannan JS, Kirkland WB (1954) Indolent cutaneous ulceration due to infection with Mycobacterium ulcerans. Med J Aust 41: 475–479.
- 26. Bolliger A, Bolliger W (1948) Experimental transission of tuberculosis to Trichosurus vulpecula. Aust J Sci 10: 182.
- 27. Fyfe JA, Lavender CJ, Johnson PD, Globan M, Sievers A, et al. (2007) Development and application of two multiplex real-time PCR assays for the detection of Mycobacterium ulcerans in clinical and environmental samples. Appl Environ Microbiol 73: 4733–4740.
- 28. Lavender CJ, Stinear TP, Johnson PDR, Azuolas J, Benbow ME, et al. (2008) Evaluation of VNTR typing for the identification of Mycobacterium ulcerans in environmental samples from Victoria, Australia. FEMS Microbiol Lett 287: 250–255.
- 29. Johnson PD, Azuolas J, Lavender CJ, Wishart E, Stinear TP, et al. (2007) Mycobacterium ulcerans in mosquitoes captured during outbreak of Buruli ulcer, southeastern Australia. Emerg Infect Dis 13: 1653–1660.
- 30. Wade H (1952) Demonstration of acid-fast bacilli in tissue sections. The Am J Pathol 28: 157.
- 31. Ross BC, Marino L, Oppedisano F, Edwards R, Robins-Browne RM, et al. (1997) Development of a PCR assay for rapid diagnosis of Mycobacterium ulcerans infection. J Clin Microbiol 35: 1696–1700.
- 32. Jackson K, Edwards R, Leslie DE, Hayman J (1995) Molecular method for typing Mycobacterium ulcerans. J Clin Microbiol 33: 2250–2253.
- 33. Ablordey A, Swings J, Hubans C, Chemlal K, Locht C, et al. (2005) Multilocus variable-number tandem repeat typing of Mycobacterium ulcerans. J Clin Microbiol 43: 1546–1551.
- 34. Hilty M, Kaser M, Zinsstag J, Stinear T, Pluschke G (2007) Analysis of the Mycobacterium ulcerans genome sequence reveals new loci for variable number tandem repeats (VNTR) typing. Microbiology 153: 1483–1487.
- 35. Doig KD, Holt KE, Fyfe JAM, Lavender CJ, Eddyani M, et al. (2012) On the origin of Mycobacterium ulcerans, the causative agent of buruli ulcer. BMC Genomics 13: 258.
- 36. Hayman J, McQueen A (1985) The pathology of Mycobacterium ulcerans infection. Pathology 17: 594–600.
- 37. Durnez L, Eddyani M, Mgode GF, Katakweba A, Katholi CR, et al. (2008) First detection of mycobacteria in african rodents and insectivores, using stratified pool screening. Appl Environ Microbiol 74: 768–773.
- 38. Durnez L, Suykerbuyk P, Nicolas V, Barriere P, Verheyen E, et al. (2010) Terrestrial small mammals as reservoirs of Mycobacterium ulcerans in Benin. Appl Environ Microbiol 76: 4574–4577.
- 39. Buddle BM, Young LJ (2000) Immunobiology of mycobacterial infections in marsupials. Dev Comp Immunol 24: 517–529.
- 40. Kerle A (2001) Possums: The Brushtails, Ringtails, and the Greater Glider: University of New South Wales Press.
- 41. Stevens CE, Hume ID (2004) Comparative Physiology of the Vertebrate Digestive System: Cambridge University Press.
- 42. Chilcott MJ, Hume ID (1985) Coprophagy and selective retention of fluid digesta: their role in the nutrition of the common ringtail possum, Pseudocheirus peregrinus. Aust J Zool 33: 1–15.
- 43. Osawa R, Blanshard WH, Ocallaghan PG (1993) Microbiological studies of the intestinal microflora of the koala, Phascolarctos cinereus. 2. Pap, a special maternal feces consumed by juvenile koalas. Aust J Zool 41: 611–620.
- 44. Vogelnest L, Stewart S, Sangster C (2012) Poxvirus infection outbreak in common ringtails (Pseudocheirus peregrinus). Aust Vet J 90: 143–145.
- 45. Jackson SJ (2003) Possums and gliders. In: Jackson SJ, editor. Australian mammals: biology and captive managment. Collingwood, Australia: CSIRO publishing. pp. 205–244
- 46. Sarfo FS, Le Chevalier F, Aka NG, Phillips RO, Amoako Y, et al. (2011) Mycolactone diffuses into the peripheral blood of Buruli Ulcer patients - implications for diagnosis and disease monitoring. PLoS Negl Trop Dis 5: e1237.
- 47. Augee ML, Smith B, Rose S (1996) Survival of wild and hand-reared ringtail possums (Pseudocheirus peregrinus) in bushland near Sydney. Wildlife Res 23: 99–108.