Difference between revisions of "Canine Distemper Virus: Wildlife Conservation Implications"

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=== Negative Sense RNA Viruses ===
 
=== Negative Sense RNA Viruses ===
  
Negative sense RNA viruses are a diverse group of pathogens that includes important human pathogens including parainfluenza viruses, influenza viruses, and respiratory syncytial virus (RSV). This group also contains important viruses for both domestic and wild animals such as Newcastle disease virus (NDV), rinderpest virus (RPV), and, the focus of this report, canine distemper virus (CDV) <ref name= Neumann> [http://www.microbiologyresearch.org/docserver/fulltext/jgv/83/11/0832635a.pdf?expires=1525821082&id=id&accname=guest&checksum=68F9ADA5BF9791C7AB514FE4DDF98C7C] </ref>.  Like all negative sense single-stranded RNA viruses, CDV must be converted to positive sense RNA by RNA-dependent RNA polymerase (RdRp) before it can be translated during replication. However, negative sense RNA viruses can be further categorized by the segmentation of their genome. As a member of the ''Paramyxoviridae'' family, CDV has a nonsegmented genome while other viruses, like influenza (''Orthomyxoviridae '' family) have segmented genomes. The main difference between the two is that nonsegmented genome replication occurs in the host's cytoplasm while segmented genome replication occurs in the host's nucleus <ref name= Conzelmann> [https://serendip.brynmawr.edu/oneworld/system/files/annreviewnegstrandvirus.pdf] </ref>. Besides ''Paramyxoviridae'', other families of negative sense RNA that have nonsegmented genomes are ''Rhabdoviridae'', ''Filoviridae '', and ''Bornaviridae'' <ref name= Neumann> [http://www.microbiologyresearch.org/docserver/fulltext/jgv/83/11/0832635a.pdf?expires=1525821082&id=id&accname=guest&checksum=68F9ADA5BF9791C7AB514FE4DDF98C7C] </ref>. Between these families, ''Rhabdoviridae'' and ''Paramyxoviridae'' possess intermediate genome sizes (10.8-14.9 kb; 15.1-15.9 kb) while ''Bornaviridae'' have the smallest genome (8.9 kb) and ''Filoviridae'' have the largest genome (19.1 kb) <ref name= Wang> [http://jvi.asm.org/content/74/21/9972.full] </ref>. The ''Paramyxoviridae'' family can be further grouped into the subfamily ''Paramyxovirinae'' which all have 6-7 transcriptional elements and a closely related amino acid sequence <ref name= para> [https://talk.ictvonline.org/ictv-reports/ictv_9th_report/negative-sense-rna-viruses-2011/w/negrna_viruses/199/paramyxoviridae] </ref>. Among this subfamily, the genus ''Morbillivirus'' can be distinguished by a lack of neuraminidase activity, the cleavage of sialic groups from glycoproteins <ref name= para> [https://talk.ictvonline.org/ictv-reports/ictv_9th_report/negative-sense-rna-viruses-2011/w/negrna_viruses/199/paramyxoviridae] </ref>.
+
Negative sense RNA viruses are a diverse group of pathogens that includes important human pathogens including parainfluenza viruses, influenza viruses, and respiratory syncytial virus (RSV). This group also contains important viruses for both domestic and wild animals such as Newcastle disease virus (NDV), rinderpest virus (RPV), and, the focus of this report, canine distemper virus (CDV) <ref name= Neumann> [http://www.microbiologyresearch.org/docserver/fulltext/jgv/83/11/0832635a.pdf?expires=1525821082&id=id&accname=guest&checksum=68F9ADA5BF9791C7AB514FE4DDF98C7C] </ref>.  Like all negative sense single-stranded RNA viruses, CDV must be converted to positive sense RNA by RNA-dependent RNA polymerase (RdRp) before it can be translated during replication. However, negative sense RNA viruses can be further categorized by the segmentation of their genome. As a member of the ''Paramyxoviridae'' family, CDV has a nonsegmented genome while other viruses, like influenza (''Orthomyxoviridae '' family) have segmented genomes. The main difference between the two is that nonsegmented genome replication occurs in the host's cytoplasm while segmented genome replication occurs in the host's nucleus <ref name= Conzelmann> [https://serendip.brynmawr.edu/oneworld/system/files/annreviewnegstrandvirus.pdf] </ref>. Besides ''Paramyxoviridae'', other families of negative sense RNA that have nonsegmented genomes are ''Rhabdoviridae'', ''Filoviridae '', and ''Bornaviridae'' <ref name= Neumann> [http://www.microbiologyresearch.org/docserver/fulltext/jgv/83/11/0832635a.pdf?expires=1525821082&id=id&accname=guest&checksum=68F9ADA5BF9791C7AB514FE4DDF98C7C] </ref>. Between these families, ''Rhabdoviridae'' and ''Paramyxoviridae'' possess intermediate genome sizes (10.8-14.9 kb; 15.1-15.9 kb) while ''Bornaviridae'' have the smallest genome (8.9 kb) and ''Filoviridae'' have the largest genome (19.1 kb) <ref name= Wang> [http://jvi.asm.org/content/74/21/9972.full] </ref>. The ''Paramyxoviridae'' family can be further grouped into the subfamily ''Paramyxovirinae'' which all have 6-7 transcriptional elements and a closely related amino acid sequence <ref name= para> [https://talk.ictvonline.org/ictv-reports/ictv_9th_report/negative-sense-rna-viruses-2011/w/negrna_viruses/199/paramyxoviridae] </ref>. Among this subfamily, the genus ''Morbillivirus'' can be distinguished by a lack of neuraminidase activity, the cleavage of sialic groups from glycoproteins <ref name= para> [https://talk.ictvonline.org/ictv-reports/ictv_9th_report/negative-sense-rna-viruses-2011/w/negrna_viruses/199/paramyxoviridae] </ref>. Neuraminidase activity is important for many negative sense RNA including influenza viruses where it promotes the release of the virus from infected cells and its spread throughout the respiratory tract <ref name= Gubareva> [https://www.sciencedirect.com/science/article/pii/S0140673699114338] </ref>.
  
 
==Description and Significance==
 
==Description and Significance==

Revision as of 02:09, 9 May 2018

By Sam Lisak

Taxonomic Information

Baltimore Classification

Group V: (−) sense single-stranded RNA virus

Higher Order Taxa[1]

Order: Mononegavirales

Family: Paramyxoviridae

Genus: Morbillivirus

Species: Canine Distemper Virus

Negative Sense RNA Viruses

Negative sense RNA viruses are a diverse group of pathogens that includes important human pathogens including parainfluenza viruses, influenza viruses, and respiratory syncytial virus (RSV). This group also contains important viruses for both domestic and wild animals such as Newcastle disease virus (NDV), rinderpest virus (RPV), and, the focus of this report, canine distemper virus (CDV) [2]. Like all negative sense single-stranded RNA viruses, CDV must be converted to positive sense RNA by RNA-dependent RNA polymerase (RdRp) before it can be translated during replication. However, negative sense RNA viruses can be further categorized by the segmentation of their genome. As a member of the Paramyxoviridae family, CDV has a nonsegmented genome while other viruses, like influenza (Orthomyxoviridae family) have segmented genomes. The main difference between the two is that nonsegmented genome replication occurs in the host's cytoplasm while segmented genome replication occurs in the host's nucleus [3]. Besides Paramyxoviridae, other families of negative sense RNA that have nonsegmented genomes are Rhabdoviridae, Filoviridae , and Bornaviridae [2]. Between these families, Rhabdoviridae and Paramyxoviridae possess intermediate genome sizes (10.8-14.9 kb; 15.1-15.9 kb) while Bornaviridae have the smallest genome (8.9 kb) and Filoviridae have the largest genome (19.1 kb) [4]. The Paramyxoviridae family can be further grouped into the subfamily Paramyxovirinae which all have 6-7 transcriptional elements and a closely related amino acid sequence [5]. Among this subfamily, the genus Morbillivirus can be distinguished by a lack of neuraminidase activity, the cleavage of sialic groups from glycoproteins [5]. Neuraminidase activity is important for many negative sense RNA including influenza viruses where it promotes the release of the virus from infected cells and its spread throughout the respiratory tract [6].

Description and Significance

Figure 1. CDV has recently been found in Amur leopard (Panthera pardus orientalis) individuals, and with only around 60 individuals remaining, this species is already the most endangered member of the Felidae family.[7].

Canine distemper virus (CDV) is a viral pathogen that is commonly known for its ability to infect domestic dogs, though it affects many other species as well. This single-stranded, negative-sense RNA virus belongs to the Paramyxoviridae family and the genus Morbillivirus [8]. CDV is highly contagious and often fatal, spreading through aerosol droplets and bodily fluids. Generally, the virus initially replicates in the respiratory tract where it enters the blood stream and spreads to lymphoid, nervous, and epithelial tissues [1]. While symptoms depend on the host species as well as the strain and severity of the virus, CDV often causes fever, ocular discharge, lethargy, anorexia, vomiting, diarrhea, seizure, paralysis, and the thickening of feet pads [9]. Although much research on this virus concentrates on its relationship with domestic dogs, CDV affects mammalian families such as Canidae (domestic and wild canids), Ursidae (bears), Pinnipeds (seals, sea lions, etc.), and Felidae (wild cats), to name a few [10]. In fact, every family in the mammalian order Carnivora is susceptible to CDV as well as various families belonging to other mammalian orders (i.e. Rodentia, Primates, Artiodactyla, and Proboscidea) [11]. Due to the wide range of potential hosts and the easy transmission pathway from domestic dogs to wildlife, as well as transmission between wildlife species, CDV poses a significant threat to the conservation efforts of many threatened mammals. Many species belonging to the Carnivora order are inherently vulnerable to extinction in the human-dominated world due to ecological and behavioral traits such as requiring large, connected tracts of habitat and preying on livestock. As such, the additional threat of CDV has important conservation implications. This report attempts to summarize current research on CDV as well as provide insight on how the virus affects wildlife, specifically, the conservation of threatened species.

Virion and Genome Structure

Figure 2. Virion and genome structure of Canine Distemper Virus[12].


All Morbilliviruses, including CDV, are virions enveloped by a lipid bilayer containing a single-stranded, negative-sense RNA genome [13]. CDV virus particles are typically between 150-300 nm in diameter [12].Their genomes code for six structural proteins in the following order: N (nucleocapsid), P(phosphoprotein), M (matrix protein), F (fusion protein), H (hemagglutinin protein), and L (large protein) (See Figure 2). They also code for V and C, two non-structural proteins [12]. The P and L proteins are coupled and attached to the N protein, which surrounds the genome to form the nucleocapsid. The P protein serves as the co-factor for the viral RNA-dependent RNA polymerase (L protein) [14]. The two glycoproteins, H and F, are spikes embedded in the lipid bilayer that mediate fusion with other cells. The envelope-associated M protein is evenly arranged underneath the lipid bilayer and regulates the two glycoproteins in addition to linking the nucleoplasmid with these proteins [14].The CDV genome consists of 15,616 nucleotides and parallels the genomes of other morbilliviruses, particularly that of its closest relative, the measles virus (MV) [15]. This genome begins with the putative regulatory 3' leader (55 nucleotides long) that directly precedes the N gene, which is then followed, sequentially, by the P, M, F, H, and L genes. Between the L gene and the end of the CDV genome (the 5' terminus), lies the putative 5' leader region (38 nucleotides long) [16]. The putative sequences direct the transcription and replication of the genome. Intergenic sequences, located at the 3' and 5' ends of every structural gene segment, control transcription termination and reinitiation [17].




Viral Ecology and Pathology

Figure 3. CDV infection in spotted hyena (Crocuta crocuta) determined by the presence of the viral antigen in the cytoplasm (arrowheads) and nuclei (arrows) of neuronal and glial cells. [18].


While the precise pathology of CDV depends on the infected species, in all species the virus is primarily transmitted through aerosols containing the virus but can also spread through bodily secretions and excretions [19]. While it is highly contagious, CDV is typically short-lived in the environment, though low temperatures can prolong the virus' survival to up to 14 days [19]. In the environment, the virus is either transmitted through direct contact (i.e. respiratory inhalations) or indirect contact (feces, urine, etc.) [20]. These potential mechanisms make transmission between unvaccinated domestic dogs almost unavoidable. Domestic dogs are the most common reservoir for spreading CDV to wildlife, however many other reservoirs species exist such as raccoons and coyotes [20] [19]. The virus is even known to spread to wildlife through the predation of reservoir species by wildlife. For example, CDV spread to tigers after they consumed unvaccinated domestic dogs [21].


CDV typically enters through the respiratory tract and, within the first 24 hours of infection, replicates in macrophages, spreading to the tonsils and bronchial lymph nodes through local lymphatics [22]. Replication of CDV in the tonsils and bronchial lymph nodes occurs 2-4 days after the initial infection. Around 4-6 days after the initial infection, the virus spreads throughout the lymphoid system [22]. The virus spreads to the central nervous system (CNS) and epithelial tissue about 8-10 days after infection [19]. The development of the canine distemper disease depends on the ability of the host immune response to clear the virus from the body's tissues. Individuals possessing cell-mediated toxicity and sufficient levels of antibody titers will usually be able to eliminate the virus from their tissues without showing signs of the disease. However, in individuals with an insufficient immune response, the virus will spread through their tissues, causing clinical signs of the disease to surface [19].

Signs and Symptoms of Canine Distemper

Figure 4. CDV causing the paralysis of the facial nerves on a domestic dog's head, leading the drooping of the edge of the mouth. [23].


The exact symptoms of CDV vary by the infected species, strain virulence, environmental conditions, host age, and host immune status. However, in all species, the virus targets the respiratory, CNS, integumentary, and gastrointestinal systems [19]. Generalized symptoms of affected animals across carnivore families include diarrhea, neurological issues, impaired immune function, and dyspnea [18], Specific symptoms of acute generalized infections, particularly common in Canidae, include pneumonia, vomiting, diarrhea, anorexia, and dehydration [22]. Other potential symptoms of CDV among Canidae are fever, ocular discharge, lethargy, and the thickening of feet pads [9]. However, infections can be difficult to detect among Felids as CDV often causes clinically silent infections and fatal disease [18]. Infection of the CNS can also lead to neurological symptoms such as muscle twitching, seizures, and occasionally paralysis (See Figure 4). Once the infection causes neurological complications like seizures, death often follows [24] [25]. CDV survival rates depend, in large part on the host species. For example, the fatality rate of infected domestic ferrets is close to 100% while 50-70% of infected domestic dogs don't even show symptoms [19].


Given the wide array of symptoms associated with CDV infection, it can be difficult to diagnose. Many diseases could potentially cause many of these same symptoms, particularly ones that also infect the respiratory, CNS, integumentary, and gastrointestinal systems. For definitive diagnosis of CDV, more in depth methods of diagnosis are required. Unfortunately, the diagnosis of CDV infection in previously vaccinated or infected individuals through serological methods can be difficult due to the potentially high antibody titers of the virus [26]. Additionally, fluorescent antibody (FA) staining in epithelial cells can produce a definitive diagnosis of CDV [26]. However, this procedure often takes several days to weeks which not a practical timescale in terms of catching and treating the disease early. Due to CDV's high mortality rates and potential to rapidly spread, a quick, sensitive method for CDV detection is required to successfully contain the virus. The most successful method for the rapid detection of CDV infection is reverse-transcriptase-polymerase chain reaction (RT-PCR). Currently the most sensitive and effective technique for CDV detection, RT-PCR can reverse transcribe target RNA into DNA from a variety of sources such as the potential host's blood, cerebrospinal fluid (CSF), and urine [27]. However, urine is easy to collect and is more useful in antemortem diagnosis of CDV infection. Urine has also been shown to be more sensitive than blood samples and at least as sensitive as CSF in the detection of CDV [27].

Prevention and Treatment of Canine Distemper

Figure 5. Nobivac® DHP, a widely available CDV vaccine [28].



The prevention of CDV, while simple in theory, is almost impossible to successfully implement. Effective vaccines exist and are the only realistic solution for controlling canine distemper in domestic dogs [29] (See Figure 5). While CDV vaccines have greatly decreased the prevalence of canine distemper in domestic dogs, the disease still spreads among unvaccinated populations including animal shelters, pet stores, and feral dogs. Additionally, many domestic dogs are suceptible to CDV if their owner forgets or declines to vaccinate their puppies with the required booster shots that are needed until the puppy reaches 16 weeks [30]. Prevention of CDV in captive wild animals can be achieved through careful vaccination, however, these vaccines must be proven to be safe for the species in question as the vaccines can occasionally have adverse effects [29]. In fact, modified-live vaccines have been known to induce CDV in nondomestic canids. Recombinant vectored vaccines are effective in many nondomestic canids, however, these vaccines must be carefully studied and implemented for each species they are used on [31]. The widespread vaccination of wild animals is obviously unfeasible, so effective conservation and wildlife management strategies must be implemented to prevent the transfer of CDV to wildlife. However, the direct vaccination of wildlife can potentially prevent the contraction of CDV for small, concentrated populations [32].


Despite the widespread prevalence of CDV vaccinations, there are currently no antiviral drugs or specific treatments for canine distemper [22]. Available treatments are symptomatic, aimed at controlling neurological dysfunction, maintaining fluid balance, and defending against secondary bacterial invasions [33]. Potential treatments include electrolyte solutions, broad-spectrum antibiotics, parenteral nutrition, antipyretics, analgesics, and anticonvulsants. However, once acute neurological symptoms of CDV appear, recovery is extremely rare [33]. Even after gastrointestinal and respiratory symptoms fade, neurological manifestations often persist. There is hope for an antiviral medication after research showed the drugs ribavarin (RBV) and interferon-alpha (IFNα) inhibit the replication of CDV in vitro [34]. Promisingly, both compounds disrupted intracellular viral replication, though further research on the antiviral efficacy of these drugs is needed to assess their clinical applicability.



Effect on Wildlife Conservation

Figure 6. Each point represents the probability (determined using 1,000 model simulations) that a tiger population will become extinct within the next 50 years. Filled points represent simulations where the population is exposed to CDV and the open points represent control simulations where populations aren't exposed to CDV. [21].
Figure 7. Black-footed ferret (Mustela nigripes) being released onto a ranch in Colorado by the Smithsonian Conservation Biology Institute. [35].


The ability of CDV to infect all terrestrial carnivore families (Mustelidae, Ursidae, Viverridae, Procyonidae, Felidae, Hyaenidae, and Canidae), in addition to various non-carnivores, allows it to threaten the conservation efforts and long-term survival of many species [19] [36]. Large predators are frequently in danger of extinction due to their reliance on large tracts of habitat, vulnerability to poaching, and frequent conflicts with humans. Exposure to CDV only exacerbates the pressure on these struggling populations of carnivores. Part of what makes CDV so dangerous to wildlife populations is its ability to spread between many species [37]. Domestic dogs are the most common reservoir for the transmission of CDV to wildlife populations. However, infected individuals of the same species in addition to other wild carnivores can also spread the virus. As the human population continues to expand, the threat of CDV to wildlife populations only grows [31].


CDV has repeatedly demonstrated the ability to drive already threatened species further towards extinction. A study on a population of Amur tigers (Panthera tigris altaica) in the Sikhote-Alin Biosphere Zapovednik (SABZ) assessed the impact of CDV on this population in addition to modelling how CDV could influence the potential extinction rates of tiger populations of various sizes. Their model found that CDV prevalance could increase the 50-year extinction probability of the tiger population in SABZ by 6.3% to 55.8% [21] (See Figure 6). The most important factors determining the model's outcome was the prevalence of CDV in reservoirs (domestic dogs and other wild carnivores) and its rate of effective contact with tigers [21]. Many endangered species only persist in small populations (relative to former levels), making them particularly susceptible to additional threats like CDV. Given the ability for CDV to jump from domestic dogs to wildlife populations, many studies have focus on monitoring populations of domestic dogs that could potentially come into contact with target species. A recent study examined the ability for CDV transmission from domestic dogs to threaten giant panda (Ailuropoda melanoleuca) populations. Their study population of pandas was found to be extremely susceptible to CDV due to a lack of an antibody for the virus in addition to living in close proximity to unvaccinated domestic dogs that have been exposed to CDV [36]. While CDV has not yet infected this population of pandas, other species have experienced large scale declines in population density directly due to CDV outbreaks. In 1994, one third of all lions (Panthera leo) in the Serengeti died from CDV, an unprecedented occurrence as prior to the outbreak, CDV had never been detected in wild lions [37]. The presence of CDV in lions was a bit puzzling given domestic dogs and lions rarely come into contact with each other. However, a study found that the virus likely spread from domestic dogs to hyenas (who often commute long distances to agricultural areas) outside the national park. The hyenas then reentered the park and spread the virus to lions [37]. This transmission route exemplifies why CDV can be so dangerous for endangered species: so many species can carry the virus, allowing it to spread very easily. Once the virus spreads throughout multiple species in any given ecosystem, containing it is very difficult.


As more and more species are pushed to the brink of extinction, conservationists are increasingly relying on ex situ conservation strategies such as captive breeding programs as last-ditch efforts to save species. Captive breeding programs can be used to establish new populations of endangered species, bolster existing ones, and preserve species' genetic diversity [38]. However, CDV not only impedes the in situ conservation efforts described above, but has devastated various captive breeding programs as well. The African wild dog (Lycaon pictus) is a critically endangered species of Canidae native to sub-Saharan Africa. In 2000, a captive breeding program of African wild dogs in Tanzania experienced an outbreak of CDV, killing 49 of 52 animals in only two months [39]. The importance of a successful breeding program is demonstrated by the rescue of the black-footed ferret (Mustela nigripes) from the brink of extinction. In 1964, scientists were ready to declare this species extinct when a small population was discovered. This population continued to decline and, in 1971, scientists started a captive breeding program after capturing individual from this population [40]. However, the majority of these captive individuals were infected with CDV and died out, as did the wild population. Conservationists received a second chance to save this species in 1981 when another population was discovered in Wyoming. Unfortunately, CDV wiped out most of this population and, in 1986, the last 18 individuals were captured to start a captive breeding program [41]. Scientists were able to prevent the outbreak of CDV in this population with terrific results. While this species is still endangered, it represents one of the greatest conservation success stories. As of 2017, there are ~300 individuals in captive breeding programs and hundreds of individuals in the wild; 4,100 ferrets have been reintroduced to the wild since 1991 [42]. Though frequent reliance of captive breeding programs will result in failures to rescue threatened species, these programs can potentially reinforce and rebuild populations of critically endangered species in the short term. Clearly, it is essential to prevent the spread of CDV to captive breeding programs if they are to successfully aid conservation efforts.

Potential Conservation Solutions

Figure 8. African lion (Panthera leo) in Serengeti National Park, Tanzania, where populations experienced a drastic decline in 1994 due to an outbreak of CDV. [43].

Two main strategies exist for the limitation of CDV outbreaks among endangered species: the vaccination of reservoirs like domestic dogs or the direct vaccination of wildlife. The creation of CDV vaccination buffer zones around vital populations of endangered species has the potential to reduce the frequency of CDV outbreaks. In 1996, after detrimental CDV outbreaks among populations of lions (Panthera leo) and African wild dogs (Lycaon pictus) in the Serengeti ecosystem, a project aimed to vaccinate domestic dogs around the national park was implemented [44]. The overall success of this project is still unclear as there has been at least one outbreak of CDV (of much lower severity) since the start of the program, but some results have been encouraging as the population has recovered. The potential reason for the persistance of CDV in this population is that it has spread to other wildlife in the ecosystem such as spotted hyena (Crocuta crocuta) and bat-eared fox (Otocyon megalotis) [44]. It will be increasingly important to establish effective buffer zones as human expansion continues to threatened endangered wildlife. Assessing the proximity of key populations of endangered species to potential reservoirs of CDV is of great importance. For example, a recent study discovered the presence of CDV infection in a population of domestic dogs that may routinely come into contact with giant pandas (Ailuropoda melanoleuca) in the Foping National Nature Reserve (FNNR) [36]. Measures can be taken to either vaccinate potential reservoirs, prevent their contact with the target wildlife species, or directly vaccinate the target wildlife species.


The direct vaccination of wildlife has proven effective both as a preventative measure and as a measure of last resort to protect small populations of endangered species severely threatened by CDV. A study researched the preventative vaccination of southern sea otters (Enhydra lutris nereis) and found it both safe and effective [45]. Direct vaccination of wildlife has also proven effective when applied to small populations where CDV is a critical factor influencing mortality rates. In 1999, the Santa Catalina Island Fox (Urocyon littoralis catalinae) population experienced a drastic decline due to CDV. The Catalina Island Fox Recovery Plan used direct vaccination, captive breeding, reintroduction, and population monitoring to grow the island's fox population from as low as 100 to ~2,000 (as of 2017) [32]. Additionally, the vaccination of captive endangered species is crucial for the long-term success of captive breeding programs. However, for nondomestic canid and many other wildlife species, modified-live vaccines are dangerous and can even induce CDV [31]. As such, recombinant vectored vaccines can provide an alternative for these species. Recombinant vectored vaccines are currently used safely on captive tigers [31]. However, just because a specific CDV vaccine is effective for one species does not mean it will be effective for another. The crash of the African wild dog (Lycaon pictus) population in a captive breeding program (detailed earlier in this report) was partly a result of the use of an effective CDV vaccine for harbor seals (Phoca vitulina) that failed for the wild dogs [39]. As such, extensive research for efficacy of specific vaccines for each species of interest is necessary. The development and administering of safe, effective vaccines for both wild and captive animals will be essential to the conservation efforts of many endangered species.


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Edited by student of Joan Slonczewski for BIOL 238 Microbiology, 2018, Kenyon College.

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