The influence of serial fecal sampling on the diagnosis of giardiasis in humans, dogs, and cats

ABSTRACT

Giardia infection is a common clinical problem in humans and pets. The diagnosis of giardiasis is challenging as hosts intermittently excrete protozoan cysts in their feces. In the present study, we comparatively evaluated two methods of serial fecal sampling in humans, dogs, and cats from Rio de Janeiro, Brazil. The Faust et al. technique was used to examine fecal specimens collected in triplicate from 133 patients (52 humans, 60 dogs, and 21 cats). Specimens from 74 patients were received from the group assigned to carry out sampling on consecutive days - 34 humans, 35 dogs, and 5 cats, and specimens from 59 patients were received from the group assigned to carry out sampling on non-consecutive, separate days - 18 human beings, 25 dogs, and 16 cats. G. duodenalis cysts were found in stools of 30 individuals. Multiple stool sampling resulted in an increase in the number of samples that were positive for Giardia in both groups. The authors therefore conclude that multiple stool sampling increases the sensitivity of the Faust et al . technique to detect G. duodenalis cysts in samples from humans, cats and dogs.

Giardia duodenalis; Fecal examination; Protozoa; Cysts

INTRODUCTION

Giardia duodenalis is a flagellated protozoan parasite that infects millions of hosts around the world ¹ causing intestinal disease in humans, companion animals and livestock ^2-4 . Giardia cysts are excreted intermittently for indefinite periods of time in the feces of both symptomatic patients and asymptomatic carriers from different species, such as humans, dogs and ruminants ^5,6 , and can remain viable and infective in the environment for several months, which contributes to the persistence and dispersion of this pathogen ^7,8 . In subclinical infections, asymptomatic carriers can shed Giardia cysts in their stools for longer periods, which favors reinfection and persistent environmental contamination ⁹ .

In recent years there has been a growing interest in the zoonotic and epidemic potential of Giardia sp. prompting greater demand for diagnostic tools ¹⁰ . Microscopic examination of fecal samples is effective and cheap, and is the most common test used to diagnose giardiasis ^11,12 . Besides giardiasis, a large variety of helminth and protozoan infections can be detected by fecal examination ^13,14 . However, the use of a single zinc sulfate flotation test in a stool sample may be insufficient to make the diagnosis of Giardia sp . infection since cyst shedding in feces is intermittent ^15-22 . Therefore, the diagnosis of giardiasis presents a challenge to parasitologists ²³ . The disease therefore may be underdiagnosed as intermittent cyst shedding can lead to a false negative result especially if only one fecal sample is examined. It is, therefore, advisable to test multiple fecal samples in order to increase the probability of getting a positive result for Giardia and avoid false negative results ^19,24 .

Given the importance of using classical parasitological methods for the diagnosis of parasitic diseases, the aim of this study was to comparatively assess two methods of serial fecal sampling, increasing the sensitivity in the diagnosis of G. duodenalis infection. Moreover, samples were collected from humans, dogs, and cats from the East Metropolitan area of Rio de Janeiro State, Southeast Brazil, to compare the efficiency of both sampling methods for each host, aiming to confirm previous studies in humans and dogs using a different methodology, and to perform the first study assessing the influence of serial sampling on feline hosts.

MATERIALS AND METHODS

In the present study, two methods of serial fecal sampling were comparatively assessed; multiple fecal samples from humans, dogs, and cats living in the East Metropolitan area of Rio de Janeiro State, Southeast Brazil, were collected between June and October 2015. The population was randomly selected among pet owners attended in veterinary clinics and veterinary clinic laboratories of Niterói . Nine hundred stool sample kits were manufactured and distributed among the individuals who volunteered to participate in this study.

The inclusion criteria for participants were the signature of a consent term and the correct collection of three fecal samples. Participants collected fecal specimens from human beings, dogs, and cats living in the city of Niterói , Rio de Janeiro State (RJ), Southeast Brazil. The cats and dogs were owned pet-animals and their feces were picked up from soil, and were collected fresh after expulsion. In addition, the volunteers who collected their feces were advised about the importance of collecting samples of the same dog/cat day by day.

Each stool sample kit consisted of 3 sampling bottles and instructions for sample collection, handling, and storage.

Two groups were formed for the collection of fecal samples from the three aforementioned species, and different sampling timings were used. Participants were assigned to each of these groups based on the random distribution of the stool sample kits among the volunteers. Half of the forms with instructions for sample collection informed participants to collect 3 fecal samples in consecutive days (daily sampling). In the other half participants were asked to collect 3 fecal samples every other day (every-other-day sampling). No preservation media were used for the storage of stool samples; these fecal specimens were kept refrigerated for a maximum of 24 h.

Fecal aliquots were analyzed using the Faust et al . ²⁵ technique for the diagnosis of giardiasis. Approximately 4 g of faeces were diluted in 20 mL of distilled water in order to obtain a homogeneous solution. After that, the samples were strained through a wire gauze onto a centrifuge glass tube and submitted to centrifugation for 2 min at 640 g. That washing step was performed twice, discarding the supernatant. Subsequently the sediment was re-suspended with 7 mL of zinc sulfate solution (sp gravity 1.200). The flotation was performed with centrifugation for 2 min at 640 g. Five loops of the convex meniscus were collected with a bacteriological loop, as recommended by Pereira and Ferreira ²⁶ . They were placed on a microscope slide, stained with a drop of Lugol’s iodine and covered with a coverslip.

The same trained clinical pathologist performed both sample preparation and microscopic examination. Each sample was numbered to allow a blind exam. In order to increase the sensitivity of the fecal flotation and improve the diagnosis of giardiasis, two slides were prepared from each sample for microscopic examination. The slides were observed at 100X magnification. To confirm the presence of Giardia cysts, a 400X magnification was used. Microscopic examination was performed up to 24 h after sample collection.

The results obtained with each of the two sampling schemes in all three species were compared using the Fisher exact test for independent variables and statistical significance was determined based on a 2-sided p-value of 0.05. The cumulative frequency of positivity was calculated considering one-, two- or three-day sampling for each host in each sampling scheme. The Fisher exact test was used to compare the calculated frequencies.

ETHICS

This study was approved by the Research Ethics Committee of the School of Medicine/Antonio Pedro University Hospital (CAAE 44055615.0.0000.5243) and by the Ethics Committee on Animal Use from the Fluminense Federal University (UFF) (Nº 643), Niterói , RJ, Brazil.

RESULTS

A total of 415 stool samples from 141 individuals were received for analysis (58 humans, 62 dogs, and 21 cats). In the daily sampling group, 74 stool samples from humans (n=34), dogs (n=35), and cats (n=5) were obtained. In the every-other-day sampling group, 59 stool samples from humans (n=18), dogs (n=25), and cats (n=16) were obtained. Eight participants did not collect all three stool samples as requested, and they were excluded from the analysis.

G. duodenalis cysts were detected on fecal samples from 30/133 patients (22.6%) evaluated by the Faust technique. In the daily sample collection scheme, 7/35 (20%) dogs and 3/5 (60%) cats were diagnosed. In the every-other-day scheme, it was possible to identify 5/25 positive (20%) dogs, 4/16 (25%) positive cats and 7/18 (38.9%) positive humans. The results obtained in each sampling scheme and for each animal species are shown in Table 1 . Fecal samples from some individuals were Giardia -negative in the first fecal examination and Giardia -positive in the second or third fecal examination.

Table 1
- Number of Giardia duodenalis -positive stool samples in each sampling scheme and in each animal species analyzed (humans, dogs, and cats). The Faust technique ¹ was used to screen fecal specimens

	Giardia -positive samples
	Daily sampling	Every-other-day sampling
Humans	0 / 34 (0%)	7 / 18 (38.9%)
Dogs	7 / 35 (20%)	5 / 25 (20%)
Cats	3 / 5 (60%)	4 / 16 (25%)
All three species	10 / 74 (13.5%)	16 / 59 (27.1%)

Serial stool sample collection increased the number of Giardia -positive fecal specimens in both, daily sampling and every-other-day sampling schemes ( Figures 1 and 2 and Table 2 ).

Figure 1
Chart showing the detection of Giardia duodenalis cysts in stool samples from all the three animal species assessed in the present study (humans, dogs, and cats), and the number of fecal specimens that were collected during the daily sampling scheme and examined using the Faust technique ¹

Figure 2
Chart showing the detection of Giardia duodenalis cysts in stool samples from all the three animal species assessed in the present study (humans, dogs, and cats), and the number of fecal specimens that were collected during the every-other-day sampling scheme and examined using the Faust technique ¹

Table 2
- Number of Giardia duodenalis -positive patients considering the number of samples collected in each sampling scheme and in each animal species analyzed (humans, dogs, and cats). The Faust technique ¹ was used to screen fecal specimens

	Giardia -positive samples
	Daily sampling			Every-other-day sampling
	S1	S1 + 2	S1 + 2 + 3	S1	S1 + 2	S1 + 2 + 3
Humans	0	0	0	5 (71.4%)	7 (100%)	7 (100%)
Dogs	3 (42.9%)	5 (71.4%)	7 (100%)	3 (60%)	3 (60%)	5 (100%)
Cats	0	1 (33.3%)	3 (100%)	0	1 (25%)	4 (100%)
All three species	3 (30%)	6 (60%)	10 (100%)	8 (50%)	11 (68.7%)	16 (100%)

When considering samples from humans regardless of the sampling group, there was an increase of 2 Giardia -positive patients with a two days sampling, an increment of 28.6% (2/7) in the detection of carriers of this protozoan infection (p=0.46). Since no human host from daily sampling group was positive, it was not possible to compare both groups for this host.

When results from dogs regardless of the sampling group were analyzed, we found that collection of two samples allowed the diagnose of 2 extra positive patients and, with the collection of three samples, 4 more Giardia -positive animals were diagnosed, with an increase of 16.7% (2/12) (p=0.44) and 33.3% (4/12) (p=0.09) in the detection of carriers, respectively. When comparing one-day sampling with three-day sampling, there was an increase of 6 Giardia -positive animals (50%) (p=0.01). In dogs, no significant difference between the two sampling schemes was observed (p=0.99).

The collection of two and three samples in the daily collection scheme provided two more positive animals each, increasing the positivity by 28.6% in the each extra sampling day scheme (p=0.59 and p=0.46, respectively). Regarding the every-other-day scheme, there was an increase of 2 positive animals only with the collection of three samples, rising the positivity by 40% (p=0.44).

An increase in the diagnostic sensitivity when multiple stool samples were examined for the presence of Giardia cysts was particularly relevant in cats: 2 (28.6%) of them were diagnosed with two collected samples (p=0.46) and the other 5 (71.4%) with three collected samples (p=0.02). No cats were diagnosed with a single sample collection. When comparing the two sampling schemes in feline samples, there was a decrease of 35.0% in the number of positive fecal specimens when using the every-other-day scheme (p=0.28). Taking into account the feline samples, it was observed that positive cats were diagnosed only with two and three collected samples, in both schemes. In the daily scheme, a percentage increase of 33.3 (p=1.00) and 66.7 (p=0.40) in each extra day of collection was observed, respectively. When samples were collected alternately, increases of 25% on the second (p=1.00) and 75% on the third day (p=0.14) of sampling collection were observed. When comparing the single sample collection with the three-day sample collection, there was a significant difference favoring the every-other-day sampling scheme (p=0.02).

When considering fecal samples from all the three species studied and from both sampling groups, there was an increase of 6 Giardia -positive patients with the two-day sampling and 9 Giardia -positive patients with the three-day sampling with an increase of 23.1% (p=0.10) and 34.6% (0.001) in the detection of carriers of this protozoan infection, respectively. When the two serial sampling schemes were compared in all animal species, there was an increase of 13.6% in the number of Giardia -positive fecal specimens if those were sampled by the every other day scheme (p=0.07).

Taking into account all three species, when stool samples were collected daily, the second and the third sample collection afforded the diagnosis of, respectively, more three and seven patients in comparison with the single collection scheme, raising the number of positive cases by 30% (p=0.21) and 70% (p=0.003). In the every-other-day scheme, it was possible to identify three more patients with two collected samples (18.7%; p=0.47) and eight more patients with three collected samples (50%; p=0.002).

Stool samples that were Giardia -positive in one assessment were Giardia -negative in other assessment; this pattern was observed in 100% of humans (7/7), 91.7% of dogs (11/12) and 100% of cats (7/7) and was present in 25 (96.2%) of 26 positive patients.

In the group in which fecal specimens were sampled on consecutive days (daily sampling), intermittent cyst shedding was observed in 100% of dogs and cats ( Figure 1 ). In the group assigned to collect fecal samples every other day (every-other-day sampling), intermittent excretion of protozoan cysts in stool was observed in 100% of humans (7/7), 80% of the dogs (4/5) and 100% of cats (4/4). In that group, 93.7% of patients (15/16) that were positive for Giardia presented intermittent cyst shedding ( Figure 2 ).

DISCUSSION

Since the same number of stool sample kits was distributed among individuals from each sampling group assessed, the difference in the number of fecal samples collected by each sampling group was due to the fact that some of the participants didn’t collect samples every other day as requested. A major drawback in parasitology research involving fecal specimen collection by volunteers is that there are participants who fail to follow the provided instructions ²⁷ . In the present study, serial sampling of multiple specimens by many individuals was an additional confounding factor.

In this study, multiple fecal sampling accounted for an increase in the number of Giardia -positive fecal samples in all three species examined and in both sampling schemes. Other authors that also assessed the influence of serial sampling on the diagnosis of giardiasis in humans ^{13,16,21,28,29} and dogs ^18,19,30,31 reported similar findings. Since no studies were observed in a comprehensive literature search, to our knowledge, this is the first study assessing the influence of serial sampling on feline hosts.

Contrary to our findings, Györkös et al . ³² , Senay and MacPherson ³³ , and Morris et al . ³⁴ reported no significant increase in the number of positive samples for intestinal parasites detection when the serial sampling scheme was used. It is important to highlight that not all of those authors studied the use of serial sample collection for diagnosing protozoa. Györkös et al . ³² performed serial fecal examination for intestinal parasites detection only in asymptomatic human carriers, and Senay and MacPherson ³³ , and Morris et al . ³⁴ tested stool samples from symptomatic human patients for enteric parasites detection. Moreover, the methods used for fecal examination and sample preservation were not standardized in these studies. Senay and MacPherson ³³ used the concentration formalin-ether technique on sodium acetate-formalin preserved samples; Morris et al . ³⁴ used the concentration by formalin-ethyl acetate method on 10% formalin and PVA preserved samples; and Györkös et al . ³² used the Faust and formalin-ether concentration techniques on sodium acetate-formalin preserved samples. It is worth noting that the authors were not expecting to specifically diagnose Giardia duodenalis infection so that a more sensitive technique for this parasite diagnosis was not used to analyze the samples. Many of intestinal parasites don’t have an intermittently shedding of ova or cysts like Giardia sp. Nevertheless, it should be emphasized that those studies were conducted in developed countries, in areas where the prevalence of Giardia is low whereas our study was conducted in a developing country (Brazil). Since epidemiological and socioeconomic features in each of these geographical areas vary significantly, different results are expected in similar assessment studies performed in each of those regions.

Smith and Wolfe ³⁵ reported that the use of triplicate fecal samples for the diagnosis of giardiasis would decrease the chance of a false negative result that would occur due to intermittent cyst excretion in humans. After that, over the years, that feature was reaffirmed by other authors, who examined the presence of Giardia cysts in infected dogs by serial evaluation of fecal samples ^18,19,31 . This finding is in agreement with the findings from our study, where the excretion of G. duodenalis cysts in the feces of 92.6% of positive volunteers was intermittent in both sampling groups and in patients from all species. The increase of Giardia -positive fecal specimens in the every-other-day sampling scheme can also be attributed to the aforementioned intermittent cyst shedding pattern of G. duodenalis .

Fecal sampling has proven to be an issue in research studies about intestinal parasites in all types of hosts ^36,37 . With regard to pets (dogs and cats), owners may be unwilling to cooperate in research and would refuse to sample fecal specimens from their animals and send those samples for parasitological examination as the odor and appearance of those stools would repulse them. In addition, the patient identification and estimating defecation time and rate can also be difficult especially in environments inhabited by many animals from different species, in particular in households with large outdoor areas that are shared by dogs and cats. Thus, the correct instruction for volunteers about sampling methods and the awareness of the pet owners about the importance of multiple fecal exams are important to ensure reliable results. Therefore, albeit sampling problems are possible in a methodology based on volunteers’ collection of samples, actions involving volunteer instructions were taken to minimize the influence of the aforementioned problems on the results.

Despite the limited number of fecal samples from each species that was analyzed in the present study, to the best of the authors’ knowledge, there are no previous studies published to date with similar methodology for sample collection (consecutive versus every-other-day) involving all three species studied.

CONCLUSIONS

Based on the results of this study, we conclude that multiple fecal sampling increases the sensitivity and accuracy of the Faust et al . ²⁵ technique to diagnose G. duodenalis infection in the three animal species examined, regardless of the sampling scheme. This procedure increases the number of tested samples but overcomes the interference of the intermittent excretion of Giardia cysts.

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Publication Dates

• Publication in this collection
  2017

History

• Received
  28 Nov 2016
• Accepted
  31 May 2017