Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Mathematical model of the dynamics of transmission and control of sporotrichosis in domestic cats

  • Aurélio A. Araújo ,

    Roles Conceptualization, Formal analysis, Methodology, Writing – original draft, Writing – review & editing

    aurelio.aquino94@gmail.com

    Affiliation Computational and Systems Biology, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brazil

  • Cláudia Codeço,

    Roles Conceptualization, Formal analysis, Methodology, Writing – original draft, Writing – review & editing

    Affiliation Scientific Computing Program, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brazil

  • Dayvison F. S. Freitas,

    Roles Conceptualization, Funding acquisition, Writing – review & editing

    Affiliation Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brasil

  • Priscila M. de Macedo,

    Roles Conceptualization, Funding acquisition, Writing – review & editing

    Affiliation Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brasil

  • Sandro A. Pereira,

    Roles Conceptualization, Funding acquisition, Writing – review & editing

    Affiliation Instituto Nacional de Infectologia Evandro Chagas, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brasil

  • Isabella D. F. Gremião,

    Roles Conceptualization, Funding acquisition, Writing – review & editing

    Affiliation Scientific Computing Program, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brazil

  • Flávio Codeço Coelho

    Roles Conceptualization, Formal analysis, Methodology, Writing – original draft, Writing – review & editing

    Affiliations Computational and Systems Biology, Fundação Oswaldo Cruz, Rio de Janeiro, Rio de Janeiro, Brazil, School of Applied Mathematics, Fundação Getulio Vargas, Rio de Janeiro, Rio de Janeiro, Brasil, Institute of Global Health, University of Geneva, Geneva, Switzerland

Abstract

Sporotrichosis is a subcutaneous mycosis with a global distribution, also known as “rose gardener’s disease”. Brazil is experiencing a rapid spread of the zoonotic transmission of of Sporothrix brasiliensis, the main etiological agent of this disease in this country, affecting domestic felines. Cost-effective interventions need to be developed to control this emergent public health problem. To allow for the comparison of alternative control strategies, we propose in this paper, a mathematical model representing the transmission of S. brasiliensis among cats, stratified by age and sex. Analytical properties of the model are derived and simulations show possible strategies for reducing the endemic levels of the disease in the cat population, with a positive impact on human health. The scenarios included mass treatment of infected cats and mass implementation of contact reduction practices, such as neutering. The results indicate that mass treatment can reduce substantially the disease prevalence, and this effect is potentialized when combined with neutering or other contact-reduction interventions. On the other hand, contact-reduction methods alone are not sufficient to reduce prevalence.

Introduction

Sporotrichosis is a neglected subcutaneous mycosis caused by species of Sporothrix Infections are typically caused by S. brasiliensis, S. schenckii or S. globosa [1, 2]. Although initially considered as a human disease, sporotrichosis was later described as a zoonotic disease [3, 4]. Countries with moderate to high burden include Brazil, Colombia, Peru and Mexico, in the Americas; South Africa, in Africa; and China, in Asia [57].

In Brazil, until the 1990’s, most reports of human sporotrichosis were in adults working in activities like gardening and planting. There were also less frequent outbreaks linked to feline sporotrichosis, mainly involving cat owners and veterinarians [8]. Since then, feline sporotrichosis has emerged as an epidemic/endemic zoonotic disease of public health concern, initially in Rio de Janeiro, but nowadays, also in other states. According to Gremião and colleagues, from 1998 to 2015, approximately 5,000 human cases were reported by the national reference center for treatment of this disease [9]. The household is the main place of transmission, and cases are concentrated among mid-aged housewives, students and elderly individuals [10]. The disease is strongly under-reported both in animals and in humans.

Many animals can be infected by the fungus, including mice, rats, squirrels, cats and dogs [11], but infections in domestic and stray cats, have been increasingly described [7, 1214]. Infected cats are the main source of infection for Sporothrix sp. in regions of zoonotic transmission. Behavioral aspects of the cat, such as fights involving scratching and biting, facilitate the transmission of this fungus [15, 16].

The strategies available to control the transmission of this fungus in the cat population and reduce risk of infection in humans, are of two types. One is focused in the screening and the treatment of infected individuals. The most common therapy is based on long-term administration of itraconazole as a monotherapy or in association with potassium iodide [17]. The second type is focused on the reduction of contact between susceptible and infected cats and the control of cat population size via neutering campaigns of females and males. Modeling the cost-effectiveness of these strategies is important to guide the development of a sporotrichosis control plan [18, 19].

In this paper, we present a mathematical description of the dynamics of sporotrichosis transmission in a population of domestic cats stratified by age and sex. The construction of the model is based on the literature on the ongoing feline sporotrichosis epidemics in Rio de Janeiro [12, 13, 17]. At the time of this writing, we found no published mathematical models of feline sporotrichosis transmission.

The model

The model takes the form of a system of ordinary differential equations describing the population dynamics of a cat population in a large city (Fig 1). The cat population was stratified in two sexes (1 = male, 2 = female), and three age classes: kitten (K) as individuals less than one year of age, young (Y) as those with 1 to 5 years, and adult (A) as those with more years of age. The natural history of the disease was described by three states: susceptible (S), infected (I), and treated (T). Once infected, cats develop the disease and eventually die from the infection since there is no spontaneous cure. Recovery, however, can be attained when cats are treated, and once cured, they return to the susceptible class.

thumbnail
Fig 1. Diagram of the transmission model of feline sporotrichosis.

Compartment structure is the same for both sexes.

https://doi.org/10.1371/journal.pone.0272672.g001

The demographic dynamics of the feline population is governed by a density dependent birth rate and density independent death rates. The birth rate, b(t), is given by Eq 1 where Y2 = SY2 + IY2 + TY2 and A2 = SA2 + IA2 + TA2. (1)

The parameter represents the environment carrying capacity for the total domestic cat population, and r is the per capita fertility rate, per month. Cats die by natural causes at age-dependent death rates mk, my, ma.

The transmission of Sporothrix between cats occurs by contacts motivated by fights between males or by sexual encounters between males and females or, less likely, by close contact between adults and kittens. We further assume that the young cats interact more frequently than the older ones. To represent these different age and sex-specific modes of transmission, we defined three types of transmission rates βK, βF and βX. Transmission to kittens is governed by the expression βK = ck pk where ck is the rate of contact between kittens and other cats and pk is the probability of transmission through this contact. The transmission rate to young males through fighting is described by the expression βF = cf pf, where cf is the fighting rate of the youngsters, and pf is the probability of transmission per fight. For adult males we multiply this transmission rate by l, an attenuation factor reflecting a lower fighting rate in adults. The transmission during sexual encounters is sex and age- specific. Transmission to young males and young females are described as βX1 = cx1 px1 and βX2 = cx2 px2, respectively, where cxi is the rate of encounters and pxi is the probability of transmission per contact. The constraints cx1 > cx2 and px2 > px1 imply that males have more sexual contacts than females, but the probability of acquiring infection is assumed to be higher in females. We further assume that older animals have less sexual contacts than the youngsters, which is represented by the attenuation factor k1 for males and k2 for females.The description of the parameters and the values used in the numerical analysis are given in Table 1.

Once the transmission rates are defined, the next step is to define the force of infection, which is the rate of new infections in each of the 6 sub-populations defined by the 3 age classes and 2 sex classes: (2a) (2b) (2c) (2d) (2e) where I* = IK1 + IK2 + IY1 + IY2 + IA1 + IA2.

The following equations describe the demographic and transmission dynamics in each age group:

Kittens

Male and female kittens are born at a rate b(t) in the susceptible class, Sk. Susceptible kittens can die of natural death or age into the young class. Infection during the first year of age occurs by contact with other animals at a rate βF. Infected kittens, Ik can die of natural infection or from sporotrichosis, or be treated and move to the Tk compartment. Treated animals can die from natural causes, or abandon the treatment and become infected again. If the animal completes the whole treatment, it may recover from the infection and move back to the susceptible compartment, since the infection does not confer immunity. (3a) (3b) (3c) (3d) (3e) (3f)

Young cats

Susceptible young males and females can die of natural cause, or age into the adult class. Young males can acquire infection from fight contacts with other youngsters or with adult males, the latter with lower probability. They can also acquire infection from sexual contacts with young and adult females, the former more frequently than the latter. As with the kittens, young infected individuals can die from other causes or from sporotrichosis, or be treated and move to the TY classes. Treated animals can abandon treatment and return to the IY compartment or recover and move to the SY compartment. (4a) (4b) (4c) (4d) (4e) (4f)

Adult cats

The equations describing the dynamics of adult cats are similar to the youngster’s. Adults face the same modes of exposure but at lower rates, since adults are considered less active. (5a) (5b) (5c) (5d) (5e) (5f)

The full model presented above, in the absence of the disease can be reduced to the following 6 equations, describing the population dynamics of the cat population and its sex and age structure. (6a) (6b) (6c) (6d) (6e) (6f)

Model parameters.

There is much uncertainty regarding many aspects of the demography of urban cats in areas where sporotrichosis is emerging. To choose reasonable values, we searched the literature and consulted with veterinarians with experience with this disease [2022]. For the numerical analysis, we considered the cat population of the Rio de Janeiro city, Brazil, a city with 6.3 million people and 2, 177, 297 households. Assuming an estimate of one cat for every 19.33 humans [23], we estimate a total population of N = 325, 918 cats. This number may be underestimated since their study only accounted for domiciled animals. Female cats have 3-5 kittens per litter, with an average of 2-3 litters per year [2426]. For this work, we considered 2 litters per year with 5 kittens each. The remaining parameters such as treatment rate (τ), treatment abandonment rate (α), cure rate (ρ), and death rate from the disease (μ) were attributed values considered reasonable for the scenarios explored, as no reliable values were available for them.

Control scenarios.

We used the model to investigate two forms of control, mass pharmacological treatment and mass neutering. Pharmacological treatment is explicitly represented in the model by the parameters τ (treatment rate), α (treatment abandonment rate) and ρ (cure rate). Neutering, on the other hand, is considered to affect mainly the contact rates for fighting and sex, cf and cx[1,2], respectively.

We considered scenarios where strategies were implemented to control the dissemination of the disease. Twelve scenarios were created, combining increased rates of treatment of infected individuals and reduced rate of contact between animals via methods such as neutering and avoiding cat’s access to the outdoor environment.

Results

Demographic dynamics of the urban feline population

The demographic dynamics described in model (7) is shown in Fig 2 using values from Table 1. The age structure of the cat population at this equilibrium is 9.52% kittens, 21.01% young, and 19.45% adults for each sex. Sex ratio is assumed 1:1 at birth and there are no sex differences in natural death rates.

thumbnail
Fig 2. Age distribution of the feline population in the equilibrium.

https://doi.org/10.1371/journal.pone.0272672.g002

We derived closed form expressions for the age-structure of the feline population at steady-state (Eq 7): (7a) (7b) (7c) where .

This equilibrium (given by 7) is stable, as the dominant eigenvalue of the system’s Jacobian matrix at this equilibrium is real and negative.

When simulating the introduction of sporotrichosis in this population, the cat population is assumed to be at this steady-state age-structure, being all individuals susceptible.

The next-generation matrix

The basic reproduction number, , measures the rate of increase of incidence upon the arrival of an infected individual in a completely susceptible population. Values above one indicate disease spread, while values below one indicate disease extinction. Deriving an expression for is important since we can assess which parameters contribute the most to transmission. One method to derive the is by computing the spectral radius of the next-generation matrix of the model. Following the methodology proposed by Van de Driessche [27], we have calculated the next-generation matrix, M = FV−1, where the matrices F and V represent the flows at the disease-free equilibrium (Eq 7), assuming the population age distribution are at the steady-state given by Eq 6. (8) (9) where , , and , being the output flow from infected compartments at each age class.

The full matrix M was omitted due to its size. A simplified version is presented instead, obtained by turning-off the treatment dynamics (τ = 0 and α = 0) and setting the aging rates to zero. The justification is that aging is a slower process compared to disease invasion and for the purposes of studying the instant of disease invasion, it could be ignored. The simplified matrix Mr(Eq 10) is: (10)

Due to the structure of M, it was not possible to derive a closed form expression for , its spectral radius. But it is possible to calculate specific numerical values, by substituting parameter values into M. For example, with the values from Table 1, .

The investigation of the matrix M itself is quite useful. Elements (i, j), i, j ∈ {Ik1, Iy1, Ia1, Ik2, Iy2, Ia2} of M can be interpreted as partial reproduction numbers of the compartments i in response to the introduction of an infected individual in the compartment j. As such, one can compute ∑j M[i, j] as the partial basic reproduction number of compartment i, that is, the expected number of secondary cases in compartment i, after the introduction of one infected individual in any of the sex and age classes. Meanwhile, a sum across the rows of M, ∑i M[i, j], produces the expected number of secondary cases on the whole population after the introduction of one index case in compartment j.

Sporotrichosis invasion in the absence of treatment

Fig 3 shows the epidemic curve of sporotrichosis after the arrival of one infected cat in the population with steady-state age structure, and . No treatment or other intervention is implemented. As the disease-free equilibrium is unstable, the infected population increases towards the endemic prevalence equilibrium, of approximately 70%, reached in a few years. The epidemic curve shape is typical of SIS models, that is, models of diseases without cure or immunity acquisition. Since all infected animals remain so until death, the observed prevalence results from the balance between infection and loss to natural and disease-induced mortality. In the absence of treatment, disease prevalence is greater among young cats, and among them, in males. This results from the higher exposure of this group to different modes of transmission.

thumbnail
Fig 3. Establishment of sporotrichosis on an entirely susceptible feline population at the demographic equilibrium shown in Fig 2, in the absence of controls.

The y-axis is scale to show the fraction of the entire population.

https://doi.org/10.1371/journal.pone.0272672.g003

In the absence of treatment, Fig 3 shows that the endemic equilibrium with 70% of prevalence can be reached within a few years. The mechanisms of transmission represented in the model, namely the role of fighting and sex in the transmission of sporotrichosis, lead to a greater importance of the young age class in establishing the Sporothrix endemic equilibrium.

Simulating control strategies

Table 2 shows the effect of control strategies on the prevalence of infection in 5 and 10 years. Important conclusions can be derived from this exercise. First, without treatment, prevalence will increase to the same equilibrium despite the implementation of contact reduction practices. Such practices affect the time to reach this equilibrium but not its magnitude. Treatment of 50% of the infected animals can reduce the prevalence to 11% (Fig 4) while 70% treatment coverage can reduce to 5% in 5 years without the need for further interventions. Disease elimination can be achieved by combining 50% of contact reduction and 50% of treatment.

thumbnail
Fig 4. Effect of a treatment rate of 0.5 on the endemic prevalences.

Y-axis represents fraction of the entire population.

https://doi.org/10.1371/journal.pone.0272672.g004

thumbnail
Table 2. Approximate prevalence after 5 and 10 years, with different combinations of treatment and neutering.

NT: no treatment, NN: no neutering or other contact reduction measures, C50: 50% neutering. Treatment levels are specified by parameters τ. *effect on sexual contacts, effect on fighting.

https://doi.org/10.1371/journal.pone.0272672.t002

Discussion

Sporotrichosis is a neglected disease in Brazil, and public health policies and strategic plans are lacking. Developing cost-effective strategies to deal with this threat is paramount as the epidemics establishes in more cities every year. This is the first model of this disease, according to our knowledge. The model proposed seeks to represent the mechanisms of transmission described in the literature [13] and by clinical observations by the authors in their clinical practice in Rio de Janeiro, Brazil. The resulting dynamics provides a very important insight into the dynamics of sporotrichosis, and could be used to inform the design of future field studies to provide more accurate measures of some parameters of the model.

Although it was not possible to derive a closed form expression for the of sporotrichosis, numeric values of can be obtained by substituting the parameter values in the next-generation matrix. Our analysis shows that sporotrichosis can establish itself very quickly in the urban population of cats with a large proportion of non-neutered animals. In such a scenario, having pharmacological treatment available can substantially slow down the establishment of the disease in a population.

Pharmacological treatment of cats with sporotrichosis, however, faces many challenges. It is expensive and requires a long period (median = 4 months) of daily administration of oral antifungal drugs. This could be difficult to implement effectively at large scale and specially in low-income regions [18]. We show that simpler interventions such as mass neutering of male and female cats can synergistically increase the effectiveness of treatment as a public health strategy. This possibility opens an avenue for the development of more integrated approaches to disease control in the cat population.

The analyses presented in this paper are limited by the uncertainty of the parameter values. More field and laboratory studies are needed to elicit more realistic values for the natural history of the disease, as well as the population dynamics of urban cats. Nevertheless, the model is already useful to explore comparative scenarios, such as control strategies combining neutering and pharmacological treatment, versus each control separately. Our results support the expected conclusion that the most effective way to keep the prevalence of sporotrichosis in any cat population is to have a quick response both in terms of diagnosis and treatment of the cats as soon as they show the first symptoms of the disease. The availability of free neutering services can aid to drive the disease to undetectable levels.

References

  1. 1. Orofino-Costa R, Macedo PM, Rodrigues AM, Bernardes-Engemann AR. The threat of emerging and re-emerging pathogenic Sporothrix species. Mycopathologia. 2020;185(5):813–842. pmid:32052359
  2. 2. Rodrigues AM, de Melo Teixeira M, de Hoog GS, Schubach TMP, Pereira SA, Fernandes GF, et al. Phylogenetic analysis reveals a high prevalence of Sporothrix brasiliensis in feline sporotrichosis outbreaks. PLoS neglected tropical diseases. 2013;7(6):e2281. pmid:23818999
  3. 3. Page CG, Frothingham L, Paige JB. Sporothrix and epizootic lymphangitis. The Journal of medical research. 1910;23(1):137. pmid:19971963
  4. 4. Meyer K. The relation of animal to human sporotrichosis: Studies on American sporotrichosis III. Journal of the American Medical Association. 1915;65(7):579–585.
  5. 5. Chakrabarti A, Bonifaz A, Gutierrez-Galhardo MC, Mochizuki T, Li S. Global epidemiology of sporotrichosis. Medical mycology. 2015;53(1):3–14. pmid:25526781
  6. 6. da Rosa ACM, Scroferneker ML, Vettorato R, Gervini RL, Vettorato G, Weber A. Epidemiology of sporotrichosis: a study of 304 cases in Brazil. Journal of the American Academy of Dermatology. 2005;52(3):451–459. pmid:15761423
  7. 7. Kovarik CL, Neyra E, Bustamante B. Evaluation of cats as the source of endemic sporotrichosis in Peru. Medical mycology. 2008;46(1):53–56. pmid:17885948
  8. 8. Gutierrez-Galhardo M, Freitas DFS, do Valle ACF. Epidemiological Aspects of Sporotrichosis Epidemic in Brazil. Curr Fungal Infect Rep. 2015;9:238–245.
  9. 9. Gremião IDF, Oliveira MME, Miranda LHM, Freitas DFS, Pereira SA. Geographic Expansion of Sporotrichosis, Brazil. Emerging Infectious Diseases. 2020;26(3):621–624. pmid:32091376
  10. 10. Freitas DF. Avaliação de fatores epidemiológicos, micológicos, clínicos e terapêuticos associados à esporotricose. Tese (Doutorado em Medicina Tropical)—Instituto Oswaldo Cruz. 2014;.
  11. 11. Pereira SA, Gremiao IDF, Menezes RC. Sporotrichosis in animals: zoonotic transmission. In: Sporotrichosis. Springer; 2015. p. 83–102.
  12. 12. de Lima Barros MB, de Oliveira Schubach A, Galhardo MCG, Schubach TMP, Reis RSd, Conceição MJ, et al. Sporotrichosis with widespread cutaneous lesions: report of 24 cases related to transmission by domestic cats in Rio de Janeiro, Brazil. International journal of dermatology. 2003;42(9):677–681. pmid:12956676
  13. 13. Barros MBdL, Schubach AdO, do Valle ACF, Galhardo MCG, Conceição-Silva F, Schubach TMP, et al. Cat-transmitted sporotrichosis epidemic in Rio de Janeiro, Brazil: description of a series of cases. Clinical Infectious Diseases. 2004;38(4):529–535. pmid:14765346
  14. 14. Dunstan RW, Langham RF, Reimann KA, Wakenell PS. Feline sporotrichosis: a report of five cases with transmission to humans. Journal of the American Academy of Dermatology. 1986;15(1):37–45. pmid:3722508
  15. 15. Montenegro H, Rodrigues AM, Dias MAG, da Silva EA, Bernardi F, de Camargo ZP. Feline sporotrichosis due to Sporothrix brasiliensis: an emerging animal infection in São Paulo, Brazil. BMC veterinary research. 2014;10(1):1–11. pmid:25407096
  16. 16. Rodrigues AM, Fernandes GF, Araujo LM, Della Terra PP, dos Santos PO, Pereira SA, et al. Proteomics-based characterization of the humoral immune response in sporotrichosis: toward discovery of potential diagnostic and vaccine antigens. PLoS neglected tropical diseases. 2015;9(8):e0004016. pmid:26305691
  17. 17. Gremião IDF, Miranda LHM, Reis EG, Rodrigues AM, Pereira SA. Zoonotic epidemic of sporotrichosis: cat to human transmission. PLoS pathogens. 2017;13(1):e1006077. pmid:28103311
  18. 18. Estrada-Castañón R, Estrada-Chávez G, Chávez-López MdG. Diagnosis and Management of Fungal Neglected Tropical Diseases In Community Settings—Mycetoma and Sporotrichosis. Tropical medicine and infectious disease. 2019;4(2):81. pmid:31100844
  19. 19. Lyon G, Zurita S, Casquero J, Holgado W, Guevara J, Brandt M, et al. Population-based surveillance and a case-control study of risk factors for endemic lymphocutaneous sporotrichosis in Peru. Clinical infectious diseases. 2003;36(1):34–39. pmid:12491199
  20. 20. Chaves A, de Campos M, Barros M, Do Carmo C, Gremião I, Pereira S, et al. Treatment abandonment in feline sporotrichosis–Study of 147 cases. Zoonoses and public health. 2013;60(2):149–153. pmid:22898261
  21. 21. Schubach TM, Schubach A, Okamoto T, Barros MB, Figueiredo FB, Cuzzi T, et al. Evaluation of an epidemic of sporotrichosis in cats: 347 cases (1998–2001). Journal of the American Veterinary Medical Association. 2004;224(10):1623–1629. pmid:15154732
  22. 22. Nascimento JMV. Estudo de intervenção em Educação em Saúde: uma estratégia para a redução do abandono de tratamento da esporotricose felina. Fundação Oswaldo Cruz, Instituto Nacional de Infectologia Evandro Chagas. Rio de Janeiro; 2019.
  23. 23. Canatto BD, Silva EA, Bernardi F, Mendes MCNC, Paranhos NT, Dias RA. Caracterização demográfica das populações de cães e gatos supervisionados do município de São Paulo. Arquivo Brasileiro de Medicina Veterinária e Zootecnia. 2012;64(6):1515–1523.
  24. 24. Papa CE. Embryo tecnology in conservation efforts for endangered felids. PUBMED. 2020;53(1):163–174.
  25. 25. Jemmett J, Evans J. A survey of sexual behaviour and reproduction of female cats. Journal of Small Animal Practice. 1977;18(1):31–37. pmid:853730
  26. 26. DIAS CGA. Características reprodutivas durante a cópula, gestação, pósparto e estudo das relações materno-filiais em gatos domésticos (Felis silvestris catus) mantidos em gatil experimental sob fotoperíodo equatorial natural. Universidade Estadual do Ceará. 2006;.
  27. 27. Van den Driessche P, Watmough J. Reproduction numbers and sub-threshold endemic equilibria for compartmental models of disease transmission. Mathematical biosciences. 2002;180(1-2):29–48. pmid:12387915