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Outbreak vaccination
Modification of routine vaccination protocols to rapidly protect animals in a high-risk population
Seven considerations when developing an outbreak vaccination protocol
1.) Vaccine type
2.) Route
3.) Starting age
4.) Frequency
5.) Time to protective immunity
6.) Timing relative to exposure
7.) Risks
Primary priority in shelter medicine
Population health over individual animal health
Why do shelter vaccination protocols differ from routine GP protocols?
Animals have unknown vaccination histories, frequent movement, close contact, and increased exposure to infectious diseases
Main goal of vaccination during an outbreak
Establish protective immunity as quickly as possible to limit disease transmission
Three major differences between routine GP and shelter juvenile vaccination
1.) Earlier starting age
2.) Shorter vaccination intervals
3.) Later final dose
Routine GP juvenile vaccination interval
Every 3-4 weeks
High-risk shelter juvenile vaccination interval
Every 2 weeks
Why are vaccination intervals shortened in shelters?
To minimize the time animals remain susceptible in a high-exposure environment
Feline panleukopenia (FPV)
A highly contagious viral disease of cats that can cause severe illness and death, especially in kittens
Three pathogens covered by FVRCP:
1.) Feline herpesvirus-1
2.) Feline calicivirus
3.) Feline panleukopenia virus
Three feline populations requiring an updated shelter vaccination protocol:
1.) Kittens
2.) Adult cats
3.) Pregnant queens
Recommended FVRCP vaccine for shelter kittens
Modified-live (MLV), SQ
Earliest recommended age to begin FVRCP in high-risk shelter kittens
4 weeks
Recommended FVRCP frequency in shelter kittens
Every 2 weeks
Age through which shelter kittens should continue receiving FVRCP
20 weeks
Recommended timing of initial FVRCP in shelter kittens
Immediately at intake, if age-appropriate
Why begin shelter kitten vaccination at 4 weeks instead of 8 weeks?
To establish protection as early as possible in a high-risk population
Why continue shelter kitten vaccination through 20 weeks?
Some kittens retain interfering maternal antibodies through approximately 16 weeks; since age at intake is unknown continuing to vaccinate until 20 weeks eliminates potential maternal antibody interference
Most important factor when determining completion of a juvenile vaccine series
Timing of the final vaccine, not the total number of doses
Why is the number of vaccines administered less important than their timing?
Multiple early doses may be ineffective if maternal antibodies are still interfering
Shelter kitten FVRCP protocol (all together)
SQ MLV vaccine beginning at 4 weeks, repeated every 2 weeks through 20 weeks; vaccinate at intake
Recommended FVRCP vaccine for adult shelter cats
SQ modified-live
Assumption regarding an adult shelter cat with unknown vaccination history
Assume it has never been vaccinated
Recommended initial FVRCP protocol for adult shelter cats with unknown history
First dose at intake, second dose approximately 2 weeks later
Two major risks of modified-live FVRCP vaccination during pregnancy
1.) Abortion
2.) Fetal abnormalities, including cerebellar hypoplasia
Routine GP recommendation for modified-live FVRCP in pregnant queens vs shelter outbreak setting
In GP, generally avoid giving modified live vaccines to pregnant animals (instead do killed vaccines)
However, in shelter situation, use MLV despite reproductive risks because protecting the shelter population is more important
Main disadvantage of killed FVRCP during an active outbreak
Protection develops more slowly because an initial dose and booster are required
Approximate time to protective immunity with killed FVRCP
7-14 days after the second dose
Why may killed FVRCP be inadequate for a heavily pregnant queen during an outbreak?
She may give birth before protective immunity develops
Alternative management option for pregnant queens discussed in lecture
Spay-abort followed by vaccination, depending on shelter policy
Three FVRCP formulations/routes
1.) MLV SQ
2.) MLV IN
3.) Killed SQ
Preferred FVRCP route for preventing feline panleukopenia
Subcutaneous
Why is SQ FVRCP preferred over IN for panleukopenia?
It provides more effective systemic protection against FPV
Approximate time to protective immunity for the initial SQ MLV FVRCP series
7-14 days after the second dose
Three groups in which SQ MLV FVRCP is generally avoided or used cautiously in routine GP
1.) Pregnant cats
2.) Kittens younger than 4 weeks
3.) Retroviral-positive cats
Primary benefit of IN FVRCP
Rapid and local protection against respiratory disease
Why does IN vaccination stimulate local respiratory protection?
It stimulates mucosal immunity at the site where respiratory pathogens enter
Major antibody associated with local mucosal immunity
IgA
Major limitation of IN FVRCP
Less effective against panleukopenia than SQ vaccination
Possible adverse effect of IN FVRCP
Transient upper respiratory signs
When might IN and SQ FVRCP be used simultaneously?
During an outbreak when both respiratory and systemic FPV protection are desired
Two patient populations in which killed FVRCP is generally considered safer
1.) Pregnant cats
2.) Retroviral-positive cats
Major disadvantage of killed FVRCP compared with MLV during an outbreak
Requires a booster and takes longer to establish protection
FVRCP formulations (all together)
-MLV SQ: preferred for FPV
-MLV IN: rapid respiratory protection
-killed SQ: safer for certain high-risk individuals but slower protection
Recommended timing of shelter vaccination relative to intake
Immediately upon arrival; ideally before entering the shelter population
Five core feline vaccines/pathogens discussed
1.) FHV-1
2.) FCV
3.) FPV
4.) Rabies
5.) FeLV in cats younger than 1 year
Three non-core feline vaccines:
1.) FeLV in cats older than 1 year
2.) Chlamydia felis
3.) Bordetella bronchiseptica
Why are non-core vaccines used selectively in shelters?
Animals may be adopted before the initial series has time to establish protection
Two circumstances that may justify additional non-core vaccines in a shelter
1.) Active outbreak
2.) Increased individual or population risk
Approximate time to protective immunity for many non-core vaccines discussed
10-14 days after the second dose
Feline leukemia virus (FeLV)
A retrovirus that can cause immunosuppression and other serious diseases in cats
Why should FeLV prevention be considered in shelters?
Cats and kittens frequently enter with unknown histories and may introduce infection into the population
Primary route of FeLV transmission
Close contact involving infected saliva
Three activities that can facilitate FeLV transmission
1.) Mutual grooming
2.) Nose-to-nose contact
3.) Sharing food/water bowls
Two FeLV vaccine types
1.) Recombinant canarypox-vector
2.) Killed
Required step before FeLV vaccination
Test for FeLV infection
FeLV vaccination classification in cats younger than 1 year
FeLV vaccination classification in cats older than 1 year
Core vaccine
Risk-based/non-core
Earliest recommended age for FeLV vaccination
8 weeks
Initial FeLV vaccination series
Two doses, 2-4 weeks apart
Approximate time to FeLV protective immunity
7-14 days after the second dose
Timing of first FeLV revaccination after the initial series
12 months after the final initial dose
FeLV vaccination protocol (all together)
Test first; begin at 8 weeks; two doses 2-4 weeks apart; revaccinate after 12 months, then according to risk
Two rabies vaccine types
1.) Killed/inactivated
2.) Recombinant canarypox-vector
Approximate time to protective immunity after a cat's first rabies vaccination
28 days
Initial rabies vaccination requirement compared with most killed vaccines
Only one initial dose is required
Protection following subsequent rabies boosters, as described in lecture
Immediate recognized protection, even if overdue
What determines rabies revaccination frequency?
Local laws and vaccine labeling
Recombinant rabies vaccine
A non-adjuvanted vaccine using a canarypox vector to deliver rabies antigen
Four major risks/challenges of shelter outbreak management
1.) Vaccination risks
2.) Movement restrictions
3.) Communication
4.) Financial/reputational consequences
Movement restriction during an outbreak
Limiting animal transfers and adoptions to reduce disease transmission
Why might animal movement need to be stopped during an outbreak?
To prevent infectious animals from spreading disease to other populations
Four negative consequences of prolonged movement restrictions
1.) Reduced adoptions
2.) Increased stress
3.) Increased secondary illness
4.) Increased housing costs
Why is rapid outbreak control particularly important in shelters?
It allows normal animal movement and adoptions to safely resume
Main concern in the boarding/daycare scenario
Dogs developing upper respiratory infections after attending the facility
Four major updates recommended for the boarding/daycare protocol
1.) Clarify vaccine requirements
2.) Add influenza/lepto
3.) Require vaccination before entry
4.) Improve screening/isolation
Major flaw in allowing dogs to receive vaccines on the day of boarding
Protective immunity has not had time to develop
Recommended general vaccination planning window before boarding
Approximately 3 weeks before entry
Recommended waiting period following the final required vaccine/booster
Approximately 2 weeks before daycare entry
Why is vaccination status alone insufficient for determining boarding eligibility?
An animal may have received its vaccines but not yet developed protective immunity
DAPP vaccine
Combination vaccine protecting against canine distemper, adenovirus, parvovirus, and parainfluenza
Four pathogens covered by DAPP
1.) Distemper
2.) Adenovirus
3.) Parvovirus
4.) Parainfluenza
Recommended DAPP vaccine type and route
Modified-live, SQ
Recommended age for the final puppy DAPP vaccine
16-20 weeks
Why is requiring at least three DAPP vaccines before daycare insufficient?
All three may have been administered too early to overcome maternal antibody interference
Most important consideration when evaluating a puppy's DAPP history
Whether the final dose was given at an appropriate age (16-20 weeks)
Recommended waiting period after the final puppy DAPP vaccine before daycare
Approximately 2 weeks
Two acceptable vaccination histories for adult dogs in the lecture's boarding protocol
1.) Completed puppy series + adult booster
2.) Appropriate initial adult series
Recommended approach for an adult dog with unknown vaccination history in the lecture
Administer an appropriate initial two-dose series
DAPP requirements for boarding (all together)
Puppies: final dose at 16-20 weeks
adults: appropriate completed series/booster history; allow time for immunity before entry
Bordetella bronchiseptica
bacterium associated with canine infectious respiratory disease complex (kennel cough)
Three Bordetella vaccination routes:
1.) Subcutaneous
2.) Oral/oral transmucosal
3.) Intranasal
SQ Bordetella vaccine type
Killed
Initial requirement for SQ Bordetella
Initial dose followed by a booster
Approximate time to protection with SQ Bordetella
2-3 weeks
Major disadvantage of SQ Bordetella in boarding facilities
Slower protection and reduced efficacy compared with preferred mucosal options
Oral Bordetella vaccine type
Modified-live
Oral transmucosal (OTM) vaccination
Administration intended to maintain vaccine contact with the oral mucosa
Respiratory pathogen not included in the oral Bordetella formulation discussed
Parainfluenza
Preferred Bordetella vaccination route for the boarding scenario
Intranasal