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Volume 23, Number 2—February 2017
Dispatch

Fatal Infection with Murray Valley Encephalitis Virus Imported from Australia to Canada, 2011

Daniel J. Niven, Kevin Afra, Mircea Iftinca, Raymond Tellier, Kevin Fonseca, Andreas Kramer, David Safronetz, Kimberly Holloway, Michael Drebot, and Andrew S. JohnsonComments to Author 
Author affiliations: University of Calgary, Calgary, Alberta, Canada (D.J. Niven, M. Iftinca, R. Tellier, K. Fonseca, A. Kramer, A.S. Johnson); Fraser Health Authority, Surrey, British Columbia, Canada (K. Afra); Provincial Laboratory for Public Health, Calgary (R. Tellier, K. Fonseca); Public Health Agency of Canada, Winnipeg, Manitoba, Canada (D. Safronetz, K. Holloway, M. Drebot)

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Abstract

Murray Valley encephalitis virus (MVEV), a flavivirus belonging to the Japanese encephalitis serogroup, can cause severe clinical manifestations in humans. We report a fatal case of MVEV infection in a young woman who returned from Australia to Canada. The differential diagnosis for travel-associated encephalitis should include MVEV, particularly during outbreak years.

In 2011, an outbreak of 17 confirmed cases of Murray Valley encephalitis (MVE) occurred in Australia, mostly in Western Australia and Northern Territory, where the virus is considered enzootic in water fowl (1). We report a travel-associated case of MVE detected in Canada related to that outbreak.

The Case-Patient

A previously healthy 19-year-old woman from Alberta, Canada, returned from Australia with increasing fatigue, fever, lethargy, and confusion. She had spent 6 months in New Zealand as part of an agricultural exchange, in which her activities included hay bundling, heavy machinery operation, and manure management but no direct zoonotic contacts.

Before returning to Canada, she took a solo 10-day vacation in Australia. Her itinerary and activities were reconstructed from tickets, receipts, and email correspondence. She flew to Darwin, in the tropical region (Top End) of Northern Territory, and then left on a 3-day tour of Kakadu, Mary River, and Litchfield National Parks. She then took a bus to Alice Springs, where she spent another 3 days touring local sites, after which she flew from Alice Springs to Calgary, Alberta, Canada, through Sydney, Australia; Auckland, New Zealand; and Los Angeles, California, USA. She was not previously vaccinated for Japanese encephalitis virus.

Symptoms of excessive fatigue developed the day of her return to Canada (day 1) and were initially attributed to jet lag. The next day, she was drowsy, confused, and febrile. The patient was admitted to a rural community hospital where empiric high-dose intravenous ceftriaxone, vancomycin, and acyclovir were administered.

Because of progressive neurologic deterioration, the patient was airlifted to Foothills Medical Centre in Calgary. On arrival (day 3), she was febrile (temperature 39.7°C) and lethargic and showed worsening confusion, incomprehensible speech, inappropriate verbal responses, and a fluctuating level of consciousness. At examination, she had mild tachypnea. She did not have nuchal rigidity, focal neurologic signs, or a rash. Initial clinical tests results are shown in Table 1. Test results for malaria were negative. Chest radiography showed fine, diffuse, interstitial markings.

Figure 1

Thumbnail of Neuroimaging during course of illness for a patient with a fatal infection of Murray Valley encephalitis virus imported from Australia to Canada, 2011. Each image corresponds to an axial cross-section through the thalamus and basal ganglia. A) Computed tomography (CT) at day 3. B) Magnetic resonance imaging (T2 flipped attenuation inversion recovery sequence) at day 3 showing abnormalities in the posterior thalami and splenium of the corpus callosum. C) CT when a fixed, dilated, rig

Figure 1. Neuroimaging during course of illness for a patient with a fatal infection of Murray Valley encephalitis virus imported from Australia to Canada, 2011. Each image corresponds to an axial cross-section through...

Results of computed tomography (CT) of the brain were within reference ranges (Figure 1, panel A). Results of cerebrospinal fluid (CSF) testing were abnormal (Table 1). Gadolinium-enhanced magnetic resonance imaging showed areas of restricted diffusion in the splenium of the corpus callosum and T2 flipped attenuation inversion recovery sequence hyperintensity in the posterior aspects of both thalami (Figure 1, panel B). A provisional diagnosis of flavivirus encephalitis was made. High-dose intravenous meropenem was given because of possible melioidosis encephalomyelitis, which has been reported in the Top End of Northern Territory (2).

The patient became increasingly agitated and had worsening hypoxemia, which required transfer to the intensive care unit for tracheal intubation and mechanical ventilation. Results of repeat chest radiography were consistent with development of the acute respiratory distress syndrome. On day 4, she began to show decerebrate posturing with increased deep tendon reflexes, diffuse rigidity, unresponsiveness, and a downward gaze preference. Repeat CT of the brain showed evolving hypodensity of both thalami with extension into the brainstem.

On day 5, a presumptive diagnosis of MVE was made on the basis of results obtained for CSF by reverse transcription PCR. Primers specific for flavivirus nonstructural protein 5 coding region (3) yielded a 770-nt sequence obtained from a 863-bp amplicon, which showed 98% identity with that of Murray Valley encephalitis virus (MVEV) strain 1–51 (GenBank accession no. AF161266).

Serum samples collected on day 4 and tested by using an ELISA were positive for MVEV IgM but negative for IgG and neutralizing antibodies (Table 2). CSF abnormalities were most pronounced on day 5 (Table 1), after which time CSF cell counts decreased rapidly. All cultures of blood, urine, CSF, and respiratory secretions were negative for MVEV. A broad investigation into possible etiologies was conducted for blood, saliva, CSF, brain tissue, and respiratory samples (Table 2).

During the ensuing 2 days, decerebrate posturing worsened, rigidity increased, and the patient became deeply comatose. Continuous electroencephalography monitoring showed onset of progressively worsening seizure activity refractory to phenytoin and levetiracetam. Infusions of intravenous diprivan and midazolam were required to produce burst-suppression (Technical Appendix Figure 1).

On day 8, a dilated, nonreactive right pupil developed. A CT scan of the brain showed marked thalamic hypodensity with sulcal effacement, acute obstructive hydrocephalus, and cerebellar tonsillar herniation (Figure 1, panel C). An emergent external ventricular drain was placed, and standard measures were taken to treat intracranial hypertension. Despite intervention, refractory intracranial hypertension developed (intracerebral pressure >70 mm H2O). A decompressive craniectomy was considered but the patient died on day 10 of worsening obstructive hydrocephalus (Figure 1, panel D) and cerebellar tonsillar herniation.

Figure 2

Thumbnail of Hematoxylin and eosin–stained autopsy specimens from a patient with a fatal infection of Murray Valley encephalitis virus imported from Australia to Canada, 2011. A) Pons showing perivascular inflammatory infiltrate (original magnification ×40). B) Thalamus showing extensive inflammation (arrows) surrounding an area of rarefaction caused by necrosis (arrowheads) and neuronal loss (original magnification ×10); inset shows a microglial nodule (original magnification ×20). C) Pyramidal

Figure 2. Hematoxylin and eosin–stained autopsy specimens from a patient with a fatal infection of Murray Valley encephalitis virus imported from Australia to Canada, 2011. A) Pons showing perivascular inflammatory infiltrate (original magnification...

Autopsy showed severe active encephalomyelitis (Figure 2). Postmortem brain biopsy specimens from the corpus callosum, upper spinal cord, and thalamus were positive for MVEV by reverse transcription PCR (Technical Appendix Figure 2) with amplicon sequences identical to those obtained from CSF. MVEV was readily isolated on Vero cells from fresh homogenates prepared from each of the 3 biopsy specimens. The genomic sequence has been deposited in GenBank under accession no. KX229766. Additional autopsy findings included lymphocytic myocarditis, pulmonary edema, and acute tubular necrosis of the kidney. The liver and spleen were congested. The pancreas and ovaries were histologically normal.

Conclusions

Historically, epidemics of MVE were recognized on the eastern coast of Australia; 6 known outbreaks were documented in the early twentieth century. Since the late 1970s, MVEV has largely been maintained in enzootic cycles involving mosquitoes and water fowl in the northern regions of Central and Western Australia; there have been multiple reported epidemics (4). Before the outbreak in 2011, heavy rains across Australia created ideal conditions for Culex annulirostris mosquitoes, the vector of MVEV, thus intensifying transmission to humans throughout the country (5). A shift in the demographic pattern of MVE cases toward non-Aboriginal, adult workers and tourists engaged in high-risk activities for mosquito exposure was observed (1). Australian States and Territories routinely use MVEV surveillance methods (mosquito monitoring, virus isolation from mosquitoes, sentinel chicken flocks, and climate surveillance) (6). Each state and territory has its own public health response and communications strategy (1), which target tourists to various degrees.

Human infection with MVEV is generally asymptomatic or mild with nonspecific symptoms, including headache, myalgia and, less commonly, rash. MVE is estimated to occur in <0.1% of infected persons but has a mortality rate of 15%–30% and produces long-term neurologic sequelae in <50% of survivors (79). Several distinct clinical patterns of MVE have been observed: encephalitis with complete recovery; cranial nerve/brainstem involvement with tremor; spinal cord involvement (poliomyelitis-like); and relentless progression to death, as seen in the patient we report (8). The presence of widespread magnetic resonance imaging abnormalities of the thalamus, midbrain, spinal cord, and cerebellum during acute illness predicted a devastating neurologic outcome (10). A novel feature of this case was the postmortem finding of viral myocarditis, which could account for early and unexpected respiratory decompensation of the patient.

Despite increased awareness of MVE, imported cases in Europe, Asia, and the Americas are rare (11). This case serves as a cautionary reminder of other viral etiologies of encephalitis that should be considered for returning travelers, although many of these etiologies might be outside the diagnostic capability of many clinical laboratories. Appropriate samples should be referred to centers in which specialized testing is available.

Dr. Niven is a specialist in critical care medicine in the Calgary Zone of Alberta Health Services, Calgary, Alberta, Canada. His major research interest is clinical and health services research for critically ill patients.

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Acknowledgment

We thank Jim Burrow, Bart Currie, Stephen Doggett, and Peter Markey for generously sharing knowledge and experiences; and the Centers for Disease Control and Prevention Fort Collins, CO, USA, for providing supplemental diagnostics for the case.

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References

  1. Selvey  LA, Dailey  L, Lindsay  M, Armstrong  P, Tobin  S, Koehler  AP, et al. The changing epidemiology of Murray Valley encephalitis in Australia: the 2011 outbreak and a review of the literature. PLoS Negl Trop Dis. 2014;8:e2656. DOIPubMed
  2. Currie  BJ, Fisher  DA, Howard  DM, Burrow  JN, Selvanayagam  S, Snelling  PL, et al. The epidemiology of melioidosis in Australia and Papua New Guinea. Acta Trop. 2000;74:1217. DOIPubMed
  3. Ayers  M, Adachi  D, Johnson  G, Andonova  M, Drebot  M, Tellier  R. A single tube RT-PCR assay for the detection of mosquito-borne flaviviruses. J Virol Methods. 2006;135:2359. DOIPubMed
  4. Mackenzie  JS, Lindsay  MD, Coelen  RJ, Broom  AK, Hall  RA, Smith  DW. Arboviruses causing human disease in the Australasian zoogeographic region. Arch Virol. 1994;136:44767. DOIPubMed
  5. Anyamba  A, Small  JL, Britch  SC, Tucker  CJ, Pak  EW, Reynolds  CA, et al. Recent weather extremes and impacts on agricultural production and vector-borne disease outbreak patterns. PLoS One. 2014;9:e92538. DOIPubMed
  6. Knope  KE, Doggett  SL, Kurucz  N, Johansen  CA, Nicholson  J, Feldman  R, et al.; National Arbovirus and Malaria Advisory Committee. Arboviral diseases and malaria in Australia, 2011-12: annual report of the National Arbovirus and Malaria Advisory Committee. Commun Dis Intell Q Rep. 2014;38:E12242.PubMed
  7. Knox  J, Cowan  RU, Doyle  JS, Ligtermoet  MK, Archer  JS, Burrow  JN, et al. Murray Valley encephalitis: a review of clinical features, diagnosis and treatment. Med J Aust. 2012;196:3226. DOIPubMed
  8. Burrow  JN, Whelan  PI, Kilburn  CJ, Fisher  DA, Currie  BJ, Smith  DW. Australian encephalitis in the Northern Territory: clinical and epidemiological features, 1987-1996. Aust N Z J Med. 1998;28:5906. DOIPubMed
  9. Broom  AK, Lindsay  MD, Plant  AJ, Wright  AE, Condon  RJ, Mackenzie  JS. Epizootic activity of Murray Valley encephalitis virus in an aboriginal community in the southeast Kimberley region of Western Australia: results of cross-sectional and longitudinal serologic studies. Am J Trop Med Hyg. 2002;67:31923.PubMed
  10. Speers  DJ, Flexman  J, Blyth  CC, Rooban  N, Raby  E, Ramaseshan  G, et al. Clinical and radiological predictors of outcome for Murray Valley encephalitis. Am J Trop Med Hyg. 2013;88:4819. DOIPubMed
  11. Stich  A, Günther  S, Drosten  C, Emmerich  P, Dwyer  DE, Hueston  L, et al. Clinical and laboratory findings on the first imported case of Murray Valley encephalitis in Europe. Clin Infect Dis. 2003;37:e1921. DOIPubMed

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Figures
Tables

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Cite This Article

DOI: 10.3201/eid2302.161161

Table of Contents – Volume 23, Number 2—February 2017

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Andrew S. Johnson, Adult Infectious Disease Residency Training Program, Departments of Medicine and Microbiology and Infectious Diseases, University of Calgary, Foothillls Medical Centre, Rm 302, 3rd Fl, North Tower, 1403 29th St NW, Calgary, AB T2N 2T9, Canada

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Page created: January 17, 2017
Page updated: January 17, 2017
Page reviewed: January 17, 2017
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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