Infectious disease is an emerging threat that conservationists are ill-equipped to manage. The threat is greatest for small populations, which can be driven to extinction by virulent pathogens; these are usually generalist pathogens that ‘spill over’ from other host species, often domestic animals. Recent attempts at disease control have taken a variety of forms, some directed at threatened hosts themselves, and others involving reservoir hosts. Thus far, few such attempts have demonstrated clear benefits of intervention, often because they were ‘crisis management’ tactics allowing no comparison with untreated controls. Design of future strategies is hampered by a lack of basic information concerning the pathogens that represent serious threats, their epidemiology in multiple-host systems, and the vaccination or treatment protocols likely to be most effective under field conditions. In general, vaccination and treatment will be most valuable in tiny populations facing very high extinction risks. However, interventions that are poorly planned or under-funded have the potential to do more harm than good. In larger populations, or over larger areas, intensive management may be inappropriate, unsustainable, or simply impractical. In these circumstances, managing population size, structure or contact between host species could offer promising alternatives to intervention.

Managing disease threats to wild mammals

An optimized reverse transcription (RT)-PCR protocol for the intravitam detection of rabies virus genomic RNA was tested with clinical samples obtained from 28 patients suspected of having rabies, 9 of whom were confirmed to have had rabies by postmortem examination. RT-PCR using saliva combined with an immunofluorescence assay performed with skin biopsy samples allowed detection of rabies in the nine patients.

Intravitam Diagnosis of Human Rabies by PCR Using Saliva and Cerebrospinal Fluid

Doubt has sometimes been cast upon the protective effect of rabies antibodies in serum. Animals and humans suffering from fatal rabies often produce high antibody titres, while rabies cases are also observed in vaccinated animals. Cellular immunity is also largely involved in protection. Nevertheless, a large number of laboratory experiments and field observations clearly demonstrate that cats and dogs which develop antibodies after vaccination and before challenge have a very high probability of surviving any challenge, no matter how strong the dose and which virus strain was used. Rabies antibody titration can, therefore, afford a strong additional guarantee to the vaccination certificates accompanying domestic carnivores during transportation between countries. Quarantine rules should also be adapted to the epidemiological features in the exporting country, e.g. statistics of vaccination failure in cats and dogs and host-virus adaptation of the rabies strains circulating in these countries.

Practical significance of rabies antibodies in cats and dogs.

A simple, sensitive, and specific polymerase chain reaction (PCR) protocol for detection of rabies virus is described. The process consists of sample preparation, reverse transcription, two-step DNA amplification, and detection of the amplified product. RNA was extracted from animal and human brain by phenol-chloroform using guanidinium thiocyanate. Viral RNA was then amplified in a two-step PCR that used two sets of nested primers designed to amplify rabies nucleocapsid (N) sequence. Rabies nucleocapsid sequence was amplified from all brain samples from 95 dogs and 3 humans with rabies confirmed by fluorescent antibody (FAT) and mouse inoculation tests (MIT). Rabies-negative brain samples (110 dogs, 2 humans) were PCR-negative. The process requires < 24 h. Detection of viral RNA was still possible in brain material that was left at room temperature for 72 h. As little as 8 pg of rabies virus RNA could be detected. This technique could have practical applications as a confirmatory test to FAT at busy rabies diagnostic centers.

Diagnosis of Rabies by Polymerase Chain Reaction with Nested Primers

The effects of ecological factors (prey, competitors, predators and disease) and intervention (immobilization, radio-collaring, and vaccination) on population size and demography were investigated in Serengeti wild dogs (Lycaon pictus), an endangered canid, between 1965 and 1991. Variation in ecological factors explained most changes in demography, but did not explain a decline in adult longevity. A significant reduction in pack life and individual longevity was coincident with the introduction of routine intervention and consistent with pathogen-induced mortality. Survival varied significantly between categories of intervention, and between individuals likely to have been exposed to different degrees of social stress before intervention. The loss of all study packs in 1991 contrasted with the persistence of breeding packs outside the study area. The cause of the demise of most study packs is unknown. Monte Carlo simulations demonstrated that population extinction was unlikely to be the consequence of chance events alone. One explanation compatible with the evidence is an outbreak of viral disease induced by stress, possibly caused by intervention.

Demography, Extinction and Intervention in a Small Population: the Case of the Serengeti Wild Dogs

Immune response to rabies vaccine in Thai dogs: a preliminary report.

Of the more than 100,000 courses of postexposure rabies treatment given in Thailand annually, 95% consist of brain tissue-derived vaccine without immune globulin. Rabies tissue culture vaccines and immune globulins are expensive by the standards of developing countries. When they are given according to either of two proven intradermal postexposure schedules, significant savings can be achieved without loss of efficacy. Purified equine rabies immune globulins account for approximately 10% of the cost of human products administered to exposed individuals and have been shown to be safe and effective. A canine preexposure immunogenicity study with a potent, inactivated tissue culture vaccine revealed that 12.5% of Thai dogs failed to develop protective antibody titers 2 months after one subcutaneous injection. Previous studies have shown significant antigenic differences between Thai street rabies virus and European and North African strains.

https://www.jstor.org/stable/info/4456038

Rabies in Thailand: 1990.

Previous studies in Thailand and Tunisia have shown that one injection of dog pre-exposure rabies vaccine does not produce a lasting antibody titre in a significant group of animals. We therefore duplicated the Thai study in a small North American community using healthy, owned dogs. A tissue culture vaccine of known high antigenicity was given intramuscularly as one primary injection and antibody titres were determined by the rapid fluorescent focus inhibition test on days 14, 30, 60, 180 and 360. Titres were less than 0.5 i.u./mL in 27% of dogs bled at 2 months, 24% at 6 months, and in 33% one year after the primary vaccination. In rabies endemic regions, it may be hazardous to rely on the previous vaccine history of a biting dog when making post-exposure management decisions. A retrospective study of antibody levels in previously vaccinated dogs in North America also indicated that a single injection of vaccine often failed to result in adequate titres.

Immune response to rabies vaccine in Alaskan dogs: failure to achieve a consistently protective antibody response

Detection of rabies antigen in canine parotid glands by dot-blot technique

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Papers

Immune response to rabies vaccine in Thai dogs: a preliminary report.

Rabies in Thailand: 1990.

Immune response to rabies vaccine in Alaskan dogs: failure to achieve a consistently protective antibody response

Detection of rabies antigen in canine parotid glands by dot-blot technique