Acta Veterinaria Brasilica. Feline neonatal toxoplasmosis and cystoisospora coinfection Case Report

Similar documents
Protozoan Parasites: Lecture 20 - Heteroxenous Coccidia - Part 1 Pages 39-51

Systemic Apicomplexans. Toxoplasma

04/02/2013. Parasites and breeding dogs: These parasites we don t hear so much about. Main internal parasites found in breeding kennels

Protozoan Parasites: Lecture 21 Apicomplexans 3 Heteroxenous Coccidia - Part 1 Pages 37-49

Above: life cycle of toxoplasma gondii. Below: transmission of this infection.

Coccidia. Nimit Morakote, Ph.D.

For Vets General Information Prevalence of Tox Prevalence of opl Tox asm opl asm Humans Hum Animals Zoonotic Risk & Other Ris Zoonotic Risk & Ot

Canine and Feline Distemper. Description. The following chart indicates the animals which are susceptible to infection by canine and feline distemp

Coccidia and Giardia Diagnosis, Prevention and Treatment

Australian and New Zealand College of Veterinary Scientists. Membership Examination. Medicine of Cats Paper 1

Outline 1/13/15. Range is mostly surrounding Puerto Rico Important for Tourism and ecological balance

Canine Anaplasmosis Anaplasma phagocytophilum Anaplasma platys

For Public Health Personnel

Feline zoonoses. Institutional Animal Care and Use Committee 12/09

Australian and New Zealand College of Veterinary Scientists. Membership Examination. Small Animal Medicine Paper 1

Diagnosing intestinal parasites. Clinical reference guide for Fecal Dx antigen testing

Diagnosing intestinal parasites. Clinical reference guide for Fecal Dx antigen testing

A:Malaria (Plasmodium species) Plasmodium falciparum causes malignant tertian malaria P. malariae: causes Quartan malaria P. vivax: causes benign

Australian and New Zealand College of Veterinary Scientists. Membership Examination. Veterinary Anaesthesia and Critical Care Paper 1

This information is intended to give guidance for vets and CP staff and volunteers in the treatment of a CP cat with diarrhoea.

How to talk to clients about heartworm disease

We Check Your Pets For Internal Parasites

Panleuk Basics Understanding, preventing, and managing feline parvovirus infections in animal shelters

Doctor B s BARF & Toxoplasmosis

LABORATORY. The Protozoa. At the Bench

Table of Contents. About the Author. Preface. Acknowledgments. Part One: Performing the Feline Physical Examination

Phylum:Apicomplexa Class:Sporozoa

Canine Distemper Virus

Control of Intestinal Protozoa in Dogs and Cats

Copper-Storage Liver Disease Basics

Control of Intestinal Protozoa in Dogs and Cats

Journal home page:

Feline Immunodefficiency Virus

Diagnosis, treatment and control: dealing with coccidiosis in cattle

Clinical Manifestations and Treatment of Plague Dr. Jacky Chan. Associate Consultant Infectious Disease Centre, PMH

JOURNAL OF INTERNATIONAL ACADEMIC RESEARCH FOR MULTIDISCIPLINARY Impact Factor 2.417, ISSN: , Volume 4, Issue 2, March 2016

Senior Pet Care and Early Disease Detection

Outline 4/25/2009. Cytauxzoonosis: A tick-transmitted parasite of domestic and wild cats in the southeastern U.S. What is Cytauxzoonosis?

AUSTRALIAN AND NEW ZEALAND COLLEGE OF VETERINARY SCIENTISTS. Sample Exam Questions. Veterinary Practice (Small Animal)

Reedy Fork Dairy Farm Parasitology Report Fall 2016

Vaccination. Why do I need to vaccinate my dog? many dogs don t survive. Several outbreaks of Parvovirus are reported in the UK each year.

What s Hiding in your Pet?

Describing characteristics of Feline Fecal Matter as it relates to Parasitic, Bacterial and Digestive maladies and infestations.

Acute Hemorrhagic Diarrhea Syndrome (AHDS) A Cause of Bloody Feces in Dogs

Seroprevalence and risk factors of infections with Neospora caninum and Toxoplasma gondii in hunting dogs from Campania region, southern Italy

Prevalence of Giardia in Household Dogs and Cats in the State of Rio de Janeiro using the IDEXX SNAP Giardia Test

Tritrichomonas Foetus in Cats

SPCA CERTIFIED. Table 1. Animal Health Response Plan. Calf mortality pre-weaning exceeds 5 % per calving season

EHRLICHIOSIS IN DOGS IMPORTANCE OF TESTING FOR CONTRIBUTING AUTHORS CASE 1: SWIGGLES INTRODUCTION WITH PERSISTENT LYMPHOCYTOSIS

Coccidia in a Shelter Setting Video Transcript July 2013

General introduction

Coccidiosis in macropods and other species

Suggested vector-borne disease screening guidelines

Professor Joe Camp June 2018

IACUC Policy on Humane Endpoints in Animal Use Proposals

Vaccines for Cats. 2. Feline viral rhinotracheitis, FVR caused by FVR virus, also known as herpes virus type 1, FHV-1

Hendra virus: Important information for all horse owners. An update on Hendra virus The Hendra vaccine

Contains most of the medically important tapeworms Scolex has 4 suckers and compact vitelline gland are characteristic Range from mm to >10m

BRUCELLOSIS. Morning report 7/11/05 Andy Bomback

Wallenpaupack Veterinary Clinic 2425 Route 6 Hawley, PA Senior Pet Care

What s Your Diagnosis? By Sohaila Jafarian, Class of 2018

SEROPREVALENCE OF BRUCELLA SPP, LEPSTOSPIRA SPP AND TOXOPLASMA GONDII IN WILD BOARD (SUS SCROFA) FROM SOUTHERN BRAZIL

Identification and Management of At- Risk Pre-fresh Cows

Fungal Disease. What is a fungus?

PARASITOLOGICAL EXAMINATIONS CATALOGUE OF SERVICES AND PRICE LIST

New Mexico Department of Agriculture

Zoonotic Diseases. Risks of working with wildlife. Maria Baron Palamar, Wildlife Veterinarian

Blood Cells of Reptiles. Blood Cells of Reptiles. Blood Cells of Reptiles. Blood Cells of Reptiles. Blood Cells of Reptiles

Feline Vaccines: Benefits and Risks

Australian and New Zealand College of Veterinary Scientists. Membership Examination. Medicine of Horses Paper 1

Australian and New Zealand College of Veterinary Scientists. Membership Examination. Veterinary Emergency and Critical Care Paper 1

What causes heartworm disease?

Australian College of Veterinary Scientists. Fellowship Examination. Feline Medicine Paper 1

HOOKWORM FAQ SHEET (rev ) Adapted from the CDC Fact Sheet

INFECTIOUS HEPATITIS, PARVOVIRUS & DISTEMPER

Hurricane Animal Hospital 2120 Mount Vernon Road Hurricane, WV or

Fact sheet. All animals, particularly herbivores, appear to be natural hosts for coccidian species with a high degree of host specificity observed.

General Approach to Infectious Diseases

Feline Wellness Report

Understanding your pet s LIVER CONDITION

Protozoan Parasites of Veterinary importance 2017

FDA Announcement. For Immediate Release. Contact. Announcement. February 13, Consumers

Dear Doctor: Our sincerest thanks, Stephen A. Connell, DVM Director, Technical, Academic and Consumer Services Elanco Companion Animal Health

Feline and Canine Internal Parasites

Proceedings of the World Small Animal Veterinary Association Sydney, Australia 2007

Index. Note: Page numbers of article titles are in boldface type.

Originally posted February 13, Update: March 26, 2018

Hydatid Cyst Dr. Nora L. El-Tantawy

Changing Trends and Issues in Canine and Feline Heartworm Infections

New Insights into the Treatment of Leishmaniasis

FELINE INFECTIOUS PERITONITIS Visions Beyond the Tip of the Iceberg!

Enteric Clostridia 10/27/2011. C. perfringens: general. C. perfringens: Types & toxins. C. perfringens: Types & toxins

Graduation: Affordable Evidence- Based Practice

Tick-borne Disease Testing in Shelters What Does that Blue Dot Really Mean?

////////////////////////////////////////// Shelter Medicine

Prescribing Guidelines for Outpatient Antimicrobials in Otherwise Healthy Children

Author - Dr. Josie Traub-Dargatz

Australian and New Zealand College of Veterinary Scientists. Fellowship Examination. Small Animal Medicine Paper 1

Apicomplexans Apicomplexa Intro

11-ID-10. Committee: Infectious Disease. Title: Creation of a National Campylobacteriosis Case Definition

Transcription:

Acta Veterinaria Brasilica June 12 (2018) 40-44 Acta Veterinaria Brasilica Journal homepage: https://periodicos.ufersa.edu.br/index.php/acta/index Case Report Feline neonatal toxoplasmosis and cystoisospora coinfection Case Report Felipe Jacques Sanches¹*, Suene Andriele da Silva Queiroz¹, Ana Paula Lourenção de Albuquerque¹, Priscila da Silva Queiroz¹, Michele Ferreira de Assis¹, Paulo Fernandes Marcusso² 1Universidade Estadual de Maringá (UEM), Campus Regional de Umuarama PR. 2Universidade Federal dos Vales do Jequitinhonha e Mucuri (UFVJM), Campus de Unaí MG. A R T I C L E I N F O Article history Received 28 January 2018 Received in revised form 12 May 2018 Accepted 14 May 2018 Keywords: Cat Kitten Acute Protozoan Zoonosis A B S T R A C T Toxoplasma gondii and Cystoisopora spp. are coccidian protozoa and compulsory intracellular parasites. These parasites present an enteric cycle phase, wild and domestic felines are definitive hosts capable of eliminating non-sporulated oocysts by faeces. Furthermore, they share the same transmission path, through the ingestion of infectious oocysts or the ingestion of cysts present on tissues. Most cat infections occur subclinically. Commonly, clinical and severe disease develops more often in kittens and immunocompromised animals. The present paper reports a case of coinfection of T. gondii and Cystoisospora spp in a feline of approximately 20 days old, weighing 260 grams, assisted at the Veterinary Hospital - UEM. The patient presented acute signs of limited mobility, remaining only in sternal position, cervical ventroflexion, dyspnea, lethargy and anorexia. T. gondii was identified through Polymerase Chain Reaction (PCR) test using a blood sample, whereas the co-analysis by flotation in saturated saline solution (Willis technique) was able to verify the presence of oocysts of Cystoisospora spp. After negative result from PCR test using stool sample, the presence of Cystoisospora spp. was confirmed, differentiating it from oocysts of T. gondii. The treatment based on sulfamethoxazole and trimethoprim was able to control the infection and decrease disease symptoms, proving to be effective and showing significant clinical improvement within 3 days after starting the treatment. INTRODUCTION Toxoplasma gondii is the most common parasitic zoonosis in humans (ELMORE et al., 2010; VIDOTTO et al., 2015). Also capable of infecting a large number of animals, such as birds and reptiles, and mammals as well. However, only felids are considered definitive hosts, able of completing the life cycle of the coccidia by eliminating non-sporulated oocysts from the faeces, which contaminate the environment and, after sporulation, become infectious for animals and humans. (MUNHOZ et al., 2017; ZULPO et al., 2018). The infection occurs after the ingestion of any of the three stages of life of the protozoa: oocysts sporulated by the ingestion of feces, tachyzoites via transplacental and / or transmamial or bradyzoites by carnivorous diet (LAPPIN, 2010). * Corresponding author: felipejaques@gmail.com Cystoisospora spp. (or Isospora), as well as T. gondii, is a coccidia that belongs to the phylum Apicomplexa. These two protozoa present similar characteristics, such as: both are compulsory intracellular parasites; present an enteric cycle phase; have the cat as the definitive host; a common transmission path, through the ingestion of infectious oocysts or the ingestion of cysts present on tissues (BRESCIANI; COELHO; PAIVA, 2015; CRYSTAL, 2009). The clinical changes observed in feline toxoplasmosis are nonspecific, including gastrenteric, respiratory, hemolymphatic, ocular, muscular and / or neurological disorders (STRITAL et al., 2016). The clinical manifestations commonly reported are: anorexia, lethargy and dyspnea, also jaundice, ascites, fever, abdominal pain, diarrhea, emesis, pneumonia, hepatitis, pancreatitis, encephalitis and neurological deficits, http://dx.doi.org/10.21708/avb.2018.12.2.7635

Sanches et al. Acta Veterinaria Brasilica March 12 (2018) 40-44 41 muscle hyperesthesia, gait stiffness and ocular lesions. (BRESCIANI et al., 2016; COSTA et al., 2015). As well as toxoplasmosis, most infections with Cystoisospora spp. are subclinical, and more susceptible and severe in kittens and immunosuppressed cats, causing symptoms such as severe diarrhea, hematochezia, loss of weight, anorexia, dehydration and death (BRESCIANI; COELHO; PAIVA, 2015; CRYSTAL, 2009). Assist in the diagnosis the clinical manifestation, hematological and biochemical exams, as well as radiographic, cytological, serological, coproparasitological and molecular exams (DUBEY; LINDSAY; LAPPIN, 2009; VIDOTTO et al., 2015). It is known that there is no therapy to cure toxoplasmosis, but there are infection control and symptom reduction, and treatments that include anti- Toxopalsma drugs such as clindamycin; sulfonamide associated with trimethoprim; and azithromycin (BRESCIANI et al., 2016; ELMORE et al., 2010; JAVINSKY, 2016; LAPPIN, 2010). In a paper written by Barbosa et al. (2012), significant therapeutic efficacy was observed with the use of enrofloxacin in vitro and in vivo models, and it could also be considered a therapeutic option for the control of toxoplasmosis. However, recurrence of the disease is always possible, since T. gondii can not be eliminated by any drug protocol (JAVINSKY, 2016; LAPPIN, 2010; NORSWORTHY; GRACE, 2009). Sulfabased therapies associated or not with trimethoprim have a good clinical response in cases of Cystoisospora spp. infections (BRESCIANI; COELHO; PAIVA, 2015; CRYSTAL, 2009; JAVINSKY, 2016). As the therapeutic response is good in most cases of toxoplasmosis, the prognosis will be good to reserved. Poor prognosis is mainly for immunosuppressed cats with liver or lung disease (LAPPIN, 2010; VIDOTTO et al., 2015). The aim of this paper is to report a case of T. gondii and Cystoisospora spp. coinfection in a newborn feline. CASE REPORT On October 18 th, 2016, was assisted by the Veterinary Hospital UEM, a feline, mongrel, approximately 20 to 25 days old, weighing 260 grams. The owner reported acute musculoskeletal weakness, lethargy, and cervical ventroflexion for less than 6 to 8 hours. The kitten had been rescued 10 days ago, along with 8 other kittens from two different litters and had been in his care ever since. Nevertheless, four kittens came to death without apparent neurological signs. Previously, the animal was in good health condition, presenting normorexia (fed with Pet Milk - milk substitute for animal feeding), which intake of the artificial milk was provided every 2 to 3 hours following label instructions and well received by the animal. The clinical symptoms had sudden onset, including: locomotor difficulty, sternal position, cervical ventroflexion, dyspnea, lethargy and anorexia. Seizure, sialorrhea, emesis and ascites, among other non-specific clinical manifestations weren t observed. Seven days before, the animal presented soft to liquid stool of lumpy appearance, with presence of striae of blood, lasting 5 days. The vermifugation had not been performed yet. On physical examination, the patient presented: rectal temperature 37.8 ºC; lung fields clear to auscultation, but dyspneic breathing; Normorritimic and normophonetic heart sounds, with rhythmic and strong arterial pulse; Oral and ocular mucosa with normal color; Absence of pain to abdominal palpation, but with moderate abdominal distension; Normohydrate; and non-reactive submandibular and popliteal lymph nodes. During the appointment the feline remained in a sternal position, presenting cervical ventroflection and muscular weakness. There were no relevant disorders during the neurological examination (present reflexes, cranial nerves intacts), but the consciousness was decreased (depressed, drowsy). Initially, glycemia was measured and was shown to be within normal reference values for the species; Hemogram and polymerase chain reaction (PCR) tests were requested for toxoplasmosis and neosporosis diagnosis; Also a coproparasitological exam. There were no significant alterations in the hemogram, and the coproparasitology was positive to Cystoisospora spp. The treatment was based on sulfamethoxazole and trimethoprim at a dose of 15mg / kg / SID - once a day, until new recommendations, considering that it was a neonate. The supportive therapy was based on supplemental vitamin (Glutamina - NutriSana) and Lactobac Cat (probiotic and prebiotic), both enteral, instituted during the treatment. Three days after the start of treatment, the owner reported total and progressive improvement in health status, and absence of the clinical disorders described previously. The PCR result confirmed the suspected of toxoplasmosis and was negative for Neospora spp. Thus, the initial treatment was maintained and prolonged for 28 days. At the end of the treatment the animal was in excellent physical condition, alert and with no clinical alterations. DISCUSSION The present report presents a case of feline toxoplasmosis and cystoisosporosis diagnosed in a

Sanches et al. Acta Veterinaria Brasilica March 12 (2018) 40-44 42 neonate. Vidotto et al. (2015) and Elmore et al. (2010) reported that the higher prevalence of the disease in kittens with congenital infection, due to transplacental transmission or during lantation, are more likely to develop clinical signs. The diarrhea reported by the owner may have resulted from the enteroepithelial replication of T. gondii, as discussed by Lappin (2010). Despite unspecific, clinical manifestations of anorexia, lethargy and dyspnea are described by Vidotto et al. (2015) and Dubey; Lindsay; Lappin (2009), and may appear suddenly. These same authors also claim that because clinical toxoplasmosis is more severe in cats infected by the transplacental route, the affected kittens may die even before weaning, which may have occurred with the other kittens that came to death. The PCR was selected as method for diagnosis, a resource provided by the hospital itself, which is a diagnostic option described by Vidotto et al. (2015). For Lappin (2010), the ideal would be to correlate the PCR with the serological test, analyzing specific antibodies for T. gondii, such as IgM and IgG, because IgM has a better correlation with clinical feline toxoplasmosis, since it is rarely present in serum of healthy cats. However, for Dubey; Lindsay; Lappin (2009), newborn cats from chronically infected mothers receive a concentration of IgG through colostrum that can persist for up to 12 weeks after birth, which might not be reliable in this case. Complementary tests performed were hemogram (table 1) and coproparasitology, suggested by Vidotto et al. (2015) and Dubey; Lindsay; Lappin (2009). Table 1 Demonstration table with values of the patient's hemogram exam, Exam realized at the Laboratory of Clinical Pathology of the Veterinary Hospital UEM. Erythrogram Results Units Reference values RBC 5,1 millions/µl 5,0-10,0 millions/µl Hemoglobin 8,2 g/dl 8-15 g/dl HCT 26,6 % 24-45 % MCV 52,2 fl 39-55 fl MCHC 30,8 g/dl 30-36 g/dl Metarybricytes % 0% PPT 6,3 g/dl 6,0-8,0 g/dl RBC normal morphology Leukogram Results Reference values % µl Percentage Absolute WBC 14.900 100 5.500-19.500 /µl Segmented neutrophils 86 12.814 35-75% 2.500-12.500/µL Neutrófilos bastonetes 0 0 0-3% 0 300/µL Metamyelocyte 0 0 0% 0 /µl Lymphocytes 11 1.639 20-55% 1.500-7.000/µL Monocytes 1 149 1-4% 0-850/µL Eosinophils 2 298 2-12% 0-1.500/µL Basophils 0 Raro Raro WBC normal morphology Thrombogram Results Reference value Platelets 492.000 200.000-500.000/uL Platelets normal morphology *RBC (red blood cells); MCV (mean corpuscular volume); MCHC (mean corpuscular hemoglobin concentration); PPT (total plasma protein); WBC (white blood cells). Coproparasitological exam is the way to detect the presence of oocysts in the faeces of animals infected by both T. gondii and Cystoisospora spp. Oocysts of Cystoisospora spp. are easily observed through centrifugal-flotation techniques using zinc sulphate solution (Faust technique) or saturated sugar solution (Sheater technique) or even flotation in saturated sodium chloride solution (Willis technique), as described by Bresciani; Bunny; Paiva (2015). They report that the main species of Cystoisospora that cause infection in felines are: Cystoisospora felis and Cystoisospora rivolta, and the size of oocysts are between 39 and 48 μm in length by 26 to 37 μm in width and 20 to 24 μm in length by 15 to 20 μm wide, respectively.

Sanches et al. Acta Veterinaria Brasilica March 12 (2018) 40-44 43 According to Javinsky (2017), the oocysts of Toxoplasma gondii are about a quarter of the size of the oocysts from Cystoisospora felis. The major difficulty in identifying T. gondii oocysts is the differentiation between Hammondia or Besnoitia spp. oocysts, since they are morphologically indistinguishable. In this case, the author proposes the use of PCR of stool sample to detect the presence or not of T. gondii oocysts. Vidotto et al. (2015) and Dubey; Lindsay; Lappin (2009) point out the difficulty of finding T. gondii oocysts, since felines eliminate these oocysts through faeces only once in their lives, with rare exceptions, and in a short period of time. The coproparasitological exam performed at the veterinary hospital was a flotation in saturated sodium chloride solution (Willis technique), sufficient to identify Cystoisospora spp. The sample was analyzed by the professor responsible for the parasitology sector of the hospital, who was able to confirm the presence of Cystoisospora spp. oocysts considering especially morphological characteristics described in literature and knowing that Cystoisospora spp. oocysts are bigger when compared to Toxoplasma gondii, through experience in the evaluations of this specific exam. PCR was also performed on the faeces of the patient in order to identify the presence of T. gondii oocysts, which resulted in a negative result. Thus, it was concluded, analysing stool sample, that only Cystoisospora spp. oocysts were identified, through coproparasitological exam. Pasty feces to lumpy liquids with traces of blood presented by the animal in this report may have been secondary to both Cystoisospora spp. and T. gondii, since diarrhea and hematochisis are symtoms of both diseases. However, none of the consulted authors reported clinical manifestations of locomotor difficulty, cervical ventroflexion and dyspnea, similar to the case described, as originating from Isosporosis. Costa et al. (2015) report that the development of clinical toxoplasmosis is associated with factors such as age, simultaneous infections, pathogenicity of the protozoal and immunosuppression. The first two factors were present in this case, since the animal had a coinfection with Cystoisospora spp. To Bresciani; Bunny; Paiva (2015), Cystoisospora spp. may contribute to complications of the clinical situation in several diseases, which probably occurred in this case. We may also consider that the kitten was probably immunosuppressed, a common characteristic in orphan. These aspects imply in an acute clinical condition and neuromuscular disorders observed. The anti-toxoplasmosis treatment based on sulfamethoxazole and trimethoprim is able to control the infection and decrease the symptomatology (BRESCIANI et al., 2016; ELMORE et al., 2010 ; VIDOTTO et al., 2015). Therefore, this protocol was used, selecting a drug that can reach significant concentrations in the central nervous system, moreover the same therapeutic protocol is effective against cystoisosporosis (BRESCIANI; PAELHO, 2015; CRYSTAL, 2009). As the patient was considered a newborn animal, Mata's guidelines were followed; Papich (2011) recommend decreasing the antibiotics dose up to 50% in these patients, thus the initial dose was lower (15mg / kg) administrated orally and daily for 7 days; starting from the second week, the interval between medications was decreased at a dose of 15mg / kg administered every 16 hours for 21 days. The treatment period (28 days) was consistent with that reported by Vidotto et al. (2015) and Lappin (2010). Glutamina (NutriSana) and Lactobac Cat (containing probiotic and prebiotic) were instituted as supportive therapy, two multivitamins composed of a combination of nutrients that helped with a fast response and improvement of the health status of the animal, besides acting as adjuvant in the microbiota recomposition of the digestive tract, since the animal had shown symptoms of enteritis. Finally, the therapeutic response was considered satisfactory and the animal exhibited significant clinical improvement within three days after treatment onset, healing after the end of the therapeutic protocol established, totaling thirty days of treatment. CONCLUSION The present paper reported a case of toxoplasmosis in a neonate feline with nonspecific and acute symptoms infected with T. gondii, detected by molecular test (PCR). The clinical status was probably aggravated due to coinfection with Cystoisospora spp., confirmed by coproparasitological examination. However, a effective and fast therapeutic response was obtained with the administration of sulfa-trimethoprim, administered for approximately 30 days, in addition to the nutritional supportive therapy. REFERENCES BARBOSA, B. F. et al. Enrofloxacin is able to control Toxoplasma gondii infection in both in vitro and in vivo experimental models. Veterinary Parasitology. v. 187, p. 44 52, 2012. BRESCIANI, K. D. S. et al. Epidemiological Aspects of Feline Toxoplasmosis. Archives of Veterinary Science. v.21, n.2, p.01-08, 2016. BRESCIANI, K. D. S.; COELHO, W. M. D.; PAIVA, F. Isosporose. In JERICÓ, M. M.; NETO, J. P. A.; KOGIKA, M. M. Tratado de Medicina Interna de Cães e Gatos. 1 ed. Rio de Janeiro: Roca, 2015. v. 1, cap. 76, p. 695-698. COSTA, R. C. B. et al. Infecção pelo toxoplasma gondii e pelo vírus da imunodeficiência felina em gatos domésticos (felis catus). Enciclopédia Biosfera, Centro Científico Conhecer - Goiânia, v.11, n.22; p. 1994, 2015.

Sanches et al. Acta Veterinaria Brasilica March 12 (2018) 40-44 44 CRYSTAL, M. A. Coccidiose. In NORSWORTHY, G. D. et al. O Paciente Felino. 3 ed. São Paulo: Roca, 2009. cap. 23, p. 50-51. DUBEY, J. P.; LINDSAY, D. S.; LAPPIN, M. R. Toxoplasmosis and other intestinal coccidial infections in cats and dogs. Vet. Clin. Small Anim. v 39, p. 1009 1034, 2009. ELMORE, S. A. et al. Toxoplasma gondii: epidemiology, feline clinical aspects, and prevention. Trends in Parasitology, v. 26, n. 4, p. 190-196, 2010. JAVINSKY, E. Sistema Digestivo, Fígado e Cavidade Abdominal: Parasitos Gastrintestinais. LITTLE, S. E. O GATO: Medicina Interna. 1 ed. Rio de Janeiro: Roca, 2016. cap. 23, p. 479-495. LAPPIN, M. R. Doenças infecciosas: Infecções Polissistêmicas por Protozoários. In NELSON, R. W.; COUTO C. G. Medicina Interna de Pequenos Animais. 4 ed. Rio de Janeiro: Elsevier, 2010. cap. 99, p. 1367-1370. MATA, J.; PAPICH, M. G. Considerações Farmacológicas em Pacientes Jovens. In PETERSON, M. E.; KUTZLER, M. A. Pediatria em Pequenos Animais. 1 ed. Rio de Janeiro: Elsevier, 2011. cap. 27, p. 233-243. MUNHOZ A. D. et al. Toxoplasmosis in cats in northeastern Brazil: Frequency, associated factors and coinfection with Neospora caninum, feline immunodeficiency virus and feline leukemia vírus. Veterinary Parasitology: Regional Studies and Reports, v. 8, p. 35 38, 2017. NORSWORTHY, G. D.; GRACE, S. F. Toxoplasmose. In NORSWORTHY, G. D. et al. O Paciente Felino. 3 ed. São Paulo: Roca, 2009. cap. 138, p. 335-336. STRITAL, A. D. et al. Estudo epidemiológico e avaliação de fatores de risco da infecção por Toxoplasma gondii e achados clinico-patológicos da infecção aguda em cães admitidos em um Hospital Escola Veterinário. Pesq. Vet. Bras. v. 36, n. 10, p. 993-998, 2016. VIDOTTO, O. et al. Toxoplasmose. In JERICÓ, M. M.; NETO, J. P. A.; KOGIKA, M. M. Tratado de Medicina Interna de Cães e Gatos. 1 ed. Rio de Janeiro: Roca, 2015. v. 1, cap.78, p. 703-712. ZULPO, D. L. et al. Toxoplasma gondii: A study of oocyst re-shedding in domestic cats. Veterinary Parasitology, v. 249, p.17 20, 2018.