Increased Risk of <i>Toxoplasma gondii</i> Infection in Patients with Colorectal Cancer in Eastern China: Seroprevalence, Risk Factors, and a Case–Control Study

Yu, Yang; Guo, Dong; Qu, Tingting; Zhao, Shuchao; Xu, Chang; Wang, Longlong; Wang, Zhongjun; Fu, Haiyang; Zhang, Xiangyan; Zhou, Na

doi:https://doi.org/10.1155/2020/2539482

BioMed Research International

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Research Article | Open Access

Volume 2020 | Article ID 2539482 | https://doi.org/10.1155/2020/2539482

Increased Risk of Toxoplasma gondii Infection in Patients with Colorectal Cancer in Eastern China: Seroprevalence, Risk Factors, and a Case–Control Study

Yang Yu,¹Dong Guo,²Tingting Qu,³Shuchao Zhao,³Chang Xu,⁴Longlong Wang,²Zhongjun Wang,¹Haiyang Fu,³Xiangyan Zhang,³and Na Zhou²

Academic Editor: Haruki Komatsu

Received29 May 2020

Revised15 Sept 2020

Accepted24 Sept 2020

Published07 Oct 2020

Abstract

The aim of this study was to explore the epidemiology of Toxoplasma gondii infection in patients with colorectal cancer (CRC) in eastern China. Therefore, 287 primary CRC patients and 287 age-matched healthy control subjects were recruited to estimate the seroprevalence of T. gondii and identify the risk factors of infection. Enzyme-linked immunoassays were used to test for anti-T. gondii immunoglobulin G (IgG) and IgM antibodies. Forty-six (16%) samples were positive for anti-T. gondii IgG antibodies in patients with CRC, compared with 26 (9.1%) in the healthy controls, a significant difference (). By contrast, eight (2.8%) patients tested positive for T. gondii IgM antibodies, compared with three (1.1%) in the controls, a difference that was not significant (). Multivariable backward stepwise logistic regression analysis revealed that a rural residence (OR 2.83; 95% CI 1.15–7.01; ) and treatment with chemotherapy (OR 2.16; 95% CI 1.02–4.57; ) were risk factors for T. gondii infection in patients with CRC. Thus, T. gondii infection is serious in patients with CRC, and a rural residence and treatment with chemotherapy are independent risk factors for infection by this parasite. Therefore, medical professionals should be aware of this pathogen in patients with CRC, and the causes of T. gondii infection in these patients need to be explored further.

1. Introduction

Colorectal cancer (CRC) is one of the most common malignancies, with the morbidity increasing steadily in recent years [1]. However, the outcome of CRC patients has improved substantially because of anticancer treatments such as surgery, chemotherapy, and targeted treatment [2]. The most common adverse effects that lead to death in malignancy patients immunocompromisation by tumors and antitumor treatments are complications associated with infection, such as those caused by bacteria and viruses [3, 4]. Parasites, especially those that cause opportunistic infections, have received relatively little attention in malignancy patients.

Toxoplasma gondii is one of the most common parasites to cause opportunistic infections, and nearly one-third of humans suffer from chronic infection worldwide [5]. The human immune system can prevent the propagation of T. gondii, and thus, an acute acquired infection is generally self-limiting and asymptomatic in healthy humans [6]. However, in immunocompromised patients, such as those with a tumor, T. gondii may cause a serious, life-threatening infection. Several studies demonstrate a latent relationship between toxoplasmosis and malignancy, including with brain and oral cancers [7–9]. In recent studies, patients with hematologic malignancies had higher seroprevalence of T. gondii antibodies [10, 11]. Moreover, in Iran, T. gondii DNA was detected in formalin-fixed, paraffin-embedded breast cancer tissue [12].

Cats are the only definitive host, and the oocysts they shed can be viable in soil for many years. Humans can develop toxoplasmosis when they ingest oocysts shed by cats or tissue cysts in other mammals [4]. Many factors are associated with toxoplasmosis in cancer patients, including contact with pigs or cats, consumption of raw or undercooked meat, and exposure to soil [9, 10, 13]. Moreover, histories of blood transfusion and chemotherapy are also risk factors for T. gondii infection in patients with malignancy [9, 14]. However, in patients with CRC, data on T. gondii infection are rare, and as a result, the prevalence of T. gondii infection and the associated risk factors in patients with CRC are unclear. Thus, this study was conducted to investigate the seroprevalence of T. gondii in patients with CRC and the association between T. gondii infection and different risk factors.

2. Methods

2.1. Subjects

Serum samples were collected from 287 primary CRC patients who presented to the Affiliated Hospital of Qingdao University (Qingdao, China) for diagnosis and treatment from May 2016 to June 2019. Patients who had received intravenous immunoglobulin therapy or immunotherapy before blood collection were excluded. The ages of the patients were from 33 to 87 years. The control subjects were 287 persons who participated in health screenings at the Affiliated Hospital of Qingdao University that were recruited and matched with CRC patients by age, gender, and location of residence.

The Ethics Committee of the Affiliated Hospital of Qingdao University approved the study (No. 2016-017-29), and all patients/guardians signed informed consent.

2.2. Sample Collection

Approximately, 5 ml of venous blood was drawn from the participants. The blood samples were centrifuged at 3,000 rpm for 10 min. Then, sera were collected in 1.5 ml Eppendorf tubes and stored at −80°C until tested for T. gondii antibodies.

2.3. Sociodemographic and Clinical Data

Sociodemographic data including age, sex, residence location, and occupation were obtained from all participants. A structured questionnaire was used to collect data on lifestyle, including any history of contact with cats, pigs, or dogs kept at home, consumption of raw or undercooked meat or vegetables and fruits, exposure to soil, and source of drinking water [7]. Clinical data that included primary locations of tumors, tumor diameter, TNM stage, histological characteristics, and histories of blood transfusion and chemotherapy were obtained from the medical records and pathological reports of the patients.

2.4. Serological Assay

Anti-T. gondii immunoglobulin G (IgG) and IgM antibodies were tested by using commercially available enzyme-linked immunosorbent assay kits (Kanghua Bio, Inc., China), following the manufacturer’s instructions. Briefly, sera diluted 1 : 400 were incubated in a T. gondii antigen-coated 96-well plate at 37°C for 20 min, followed by washing three times with distilled water, and then, 50 μl of HRP conjugate enzyme was added to each well. After washing five times, “A” (50 μl) and “B” (30 μl) solutions were added into the wells and incubated at 37°C for 10 min. The optical density (OD) was read at 450 nm using an automated microplate reader (Infinit f200, Tecan, Australia) and corrected with blank controls. The cutoff value was calculated as 2.1 times the mean negative control OD, and results equal to or greater than the cutoff value were considered positive. Positive and negative serum controls were included in every plate. The samples from patients with CRC and control subjects were randomly mixed.

2.5. Statistics

Statistical analyses were conducted using the statistical software SPSS 19.0. In the single variable analysis, a chi-squared test or Fisher exact test was used to analyze the antibody seroprevalence for various variables. The independent risk factors associated with T. gondii infection were identified by a multivariable backward stepwise logistic regression analysis. The adjusted odds ratio (OR) and 95% confidence interval (CI) were calculated to identify the effect size of risk factors. Results with were considered as statistically significant.

3. Results

The overall seroprevalence of T. gondii antibodies was 48/287 (16.7%) in CRC patients and 26/287 (9.1%) in healthy controls, a significant difference (). The seroprevalence of anti-T. gondii IgG antibodies was significantly different () between CRC patients (46/287, 16.0%) and healthy controls (26/287, 9.1%). By contrast, eight (2.8%) patients tested positive for T. gondii IgM antibodies, compared with three (1.1%) controls, a difference that was not significant (). The single variable analysis showed that T. gondii seroprevalence was associated with residence in a rural area, an advanced tumor stage, and chemotherapy treatment. A higher seroprevalence of T. gondii antibodies was found in patients ≤50 years old (22.58%) than in those 51 to 69 (15.98%) or ≥70 years old (16.13%), although the difference was not significant (). In addition, patients with a left-side colon tumor or those with a nonmucin tumor had a higher T. gondii seroprevalence, although the differences were not significant. The sociodemographic and clinical characteristics of the CRC patients and the healthy controls are shown in Table 1.

The multivariable backward stepwise logistic regression analysis revealed that residence in a rural area (OR 2.83; 95% CI 1.15–7.01; ) and chemotherapy treatment (OR 2.16; 95% CI 1.02–4.57; ) were significantly associated with T. gondii infection (Table 2).

4. Discussion

Genetic factors and physical and chemical factors are responsible for the development of CRC. Although some reports indicate a possible association between T. gondii infection and malignancies [9, 15, 16], the infection status of T. gondii in patients with CRC remains unclear in eastern China.

In this study, the T. gondii seroprevalence was significantly higher in patients with CRC (16.7%, 48/287) than in control subjects (9.1%%, 26/287) (). The T. gondii seroprevalence is higher than the 8.4% reported among 119 CRC patients in Anhui, China [17], but lower than the 21.7% reported in Hainan, China [18]. Compared with China, T. gondii seroprevalence is higher in the Middle East and Egypt, where it reaches 50% in patients with CRC [19, 20]. Several factors may be responsible for these differences, such as the sample size and the age distribution and race of patients, as well as diet and environmental factors. In addition, compared with healthy controls, patients with CRC had a higher seroprevalence of T. gondii IgG antibodies (16.0% vs. 9.1%; ), although the seroprevalence of T. gondii IgM antibodies was not significantly different between the two groups (2.8% vs. 1.1%; ). Thus, patients with malignancies more commonly harbored T. gondii infection. However, whether cancer opens a door for toxoplasmosis or toxoplasmosis promotes the development of cancer remains equivocal. Toxoplasma gondii has some rhoptry-secreted kinases that promote intracellular infection and inhibit the innate immune response in mammals [21, 22]. Toxoplasma gondii may also promote the development of brain cancer by transforming the expression of host microRNAs [23]. Moreover, in malignant tumors, there are defective both humoral and innate immune responses, and patients struggle to resist intracellular pathogen infections and are inclined to develop toxoplasmosis [22]. Thus, both toxoplasmosis and cancer are interacting. This study showed clearly that T. gondii is associated with CRC; however, the reasons for the association remain unclear, and the effects of T. gondii infection on CRC patients need to be studied further.

The rate of T. gondii infection increases with age [24, 25] and is affected by sex [16]. These associations can be explained because the possibility of infection increases with age and depends on type of occupation, often sex-related, with an opportunistic pathogen such as T. gondii. However in patients with malignancy, T. gondii is inclined to infect younger patients [10]. The reason for this association is that patients with malignancy are immune-defective, and young patients may have immune systems too frail to control opportunistic infections [7, 10]. In the present study, the T. gondii seroprevalence was highest in patients ≤50 years old, although the increase was not significant. Therefore, further studies based on larger sample sizes are needed to confirm the association between T. gondii infection and age of CRC patients.

Previous reports indicate that contact with pigs and cats, consumption of raw or undercooked meat, and exposure to soil are risk factors for T. gondii infection in cancer patients [7, 9]. In the present study, the multivariate analysis showed that patients residing in a rural area had higher seroprevalence than those residing in an urban area. Oocysts are shed by felines infected with T. gondii, and humans got infected via ingestion of oocysts. Therefore, contact with felines and drinking water contaminated with feline feces can increase the risk of T. gondii infection [26]. Rural areas are typically less developed with poor sanitation. In addition, most people who live in rural areas are farmers and are exposed to feces more frequently, thereby increasing the risk of new infection by the intracellular parasite. Although the patients that resided in rural areas had higher risk of T. gondii infection, this problem has received little attention. Therefore, there is an urgent need to appeal to the general public to take action and reduce T. gondii infection in people residing in rural areas. Additionally, in the patients from rural areas with CRC, it is essential to monitor for early signs of toxoplasmosis and to take steps to prevent T. gondii infection.

Chemotherapy is the main treatment for patients with advanced CRC, although it may cause immune system dysfunction and lead to failure of cancer therapy [27]. In fact, with chemotherapy, patients may be more susceptible to toxoplasmosis [15, 28]. Patients with malignant tumors have defective immunity, and when treated with chemotherapy, their immune systems weaken further and then fail to prevent T. gondii infection [7]. Paclitaxel and 5-fluorouracil (5-FU) are the most commonly used chemotherapy drugs for CRC. Paclitaxel activates ERK through the toll-like receptor 4-myeloid differentiation gene 88 signaling pathway, whereas 5-FU leads to the misincorporation of fluoronucleotides into RNA and DNA and inhibits the nucleotide synthetic enzyme thymidylate synthase. 5-FU-induced activation of MAPK activity is associated with increased production of IL-1, IL-6, and TNF, which may increase inflammation responses. In this study, the single variable analysis showed that patients with an advanced stage of tumor were more likely to be infected with T. gondii. Therefore, an advanced tumor stage and chemotherapy may interact in affecting the development of toxoplasmosis. Moreover, similar to other intracellular pathogens, T. gondii intracellular tachyzoites can disseminate into all organs and may disturb cellular barriers and cause irregularity in host gene expression. Thus, people with CRC may be susceptible to T. gondii and develop toxoplasmosis.

There were some limitations associated with this study. First, the dataset was relatively small and therefore did not reflect the entire Chinese population. Second, antibody-based assays may contribute to false positivity of the results as confirmatory tests based on antigen detection have not been employed in the study, so, the influence of this management for antibody seroprevalence was unclear. Third, the sera of the donors were not collected, so the positives for T. gondii antibodies caused by donor-derived antibodies were uncertain.

5. Conclusions

The present study revealed that T. gondii infection is serious in patients with CRC and that residence in a rural area and treatment with chemotherapy are independent risk factors for this parasitic infection. Thus, doctors should be careful with this pathogen in patients with CRC, and the causes of T. gondii infection in those patients need to be explored further.

Data Availability

Requests for access to individual subject data may be made to Na Zhou; please send an email to zhou_na_love@126.com.

Disclosure

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Conflicts of Interest

The authors declare that there are no conflicts of interest.

Acknowledgments

This study was supported by the Shandong Provincial Natural Science Foundation, China (ZR2016HQ18).

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Copyright © 2020 Yang Yu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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